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<title>Biotechnology</title>
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<prism:eIssn>1682-2978</prism:eIssn>
<prism:publicationName>>Biotechnology</prism:publicationName>
<prism:issn>1682-296X</prism:issn>
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<image rdf:about="http://198.170.104.138/org_img/logo-1-3.gif">
<title>Biotechnology</title>
<url>http://198.170.104.138/org_img/logo-1-3.gif</url>
<link>http://www.ansijournals.com</link>
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<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4518">
<title><![CDATA[Effects of Different Fixation Devices on Fracture Treatment and Evaluation by Radiography in Birds  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4518</link>
<description><![CDATA[Twenty star crossbred broilers of 5 weeks age were taken and divided into 4 groups to know the suitable method of fracture immolization. The fixation devices used were adhesive tape with wood splint, intramedullary pinning and dynamic compression plate with cortical screws and one group as control kept in case rest. To monitor the healing status, the radiographs were taken at 3rd, 4rd and 6rd postoperative weeks. Minimal fracture gap, callus formation and excellent alignment were found in dynamic compression plate. Fracture gap reduces significantly (P<0.01) with small callus formation and good alignment in dynamic compression plate group but similar result along with larger callus found in intramedullary group. The present study suggested that dynamic compression plate is the best method for fixation of fractured bone in birds.
 ]]></description>
<dc:creator>M.M. Islam, M.M. Rahman, D. Biswas, M.M. Rahman and M.A. Haque </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Effects of Different Fixation Devices on Fracture Treatment and Evaluation by Radiography in Birds  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>9</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>1</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4519">
<title><![CDATA[Biosynthesis of Xylanase by UV-Treated Mutant Strain of <I>Aspergillus niger</I> GCBMX-45  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4519</link>
<description><![CDATA[This investigation describes the biosynthesis of xylanase by UV-treated strain of <I>Aspergillus niger</I>  GCBMX-45. For this purpose, parental strains of Aspergillus niger was UV- irradiated for different time intervals (5-60 minutes). It was found that the strain treated for 45minutes gave the maximum yield of xylanase when different parameters were employed. Among different substrates and carbon sources, wheat bran (10g) and sucrose, respectively gave maximum production. Distilled water as a diluent and incubation period of 72 hours at 30<sup>o</sup>C were optimized for improved production under solid substrate fermentation conditions.
 ]]></description>
<dc:creator>Waseem Ahmad Butt, Ikram-ul-Haq and Javed Iqbal  </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Biosynthesis of Xylanase by UV-Treated Mutant Strain of <I>Aspergillus niger</I> GCBMX-45  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>14</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>10</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4520">
<title><![CDATA[Effects of Nutrients on the Extracellular Lipase Production by Mutant Strain of <I>Rhizopus oligosporous </I>T<sup>UV</sup>-31 ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4520</link>
<description><![CDATA[Mutant strain of <I>Rhizopus oligosporous</I> T<sup>UV</sup>-31 was used for the production of extracellular lipase by solid-state fermentation. Maximum lipase activity (76.69 /g) was observed when different nutrients were added to the substrate. Among different carbon sources Tween 80 at 0.5% was found to be the best carbon source. The best organic and inorganic nitrogen sources for lipolytic activity were soybean meal (1%) and ammonium sulphate (0.4%) respectively. Addition of egg yolk to fermentation medium enhanced the lipase production.
]]></description>
<dc:creator>Tehreema Iftikhar and Athar Hussain</dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Effects of Nutrients on the Extracellular Lipase Production by Mutant Strain of <I>Rhizopus oligosporous </I>T<sup>UV</sup>-31 ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>20</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>15</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4521">
<title><![CDATA[Spectroscopic Study of Porphyrin Production and Accumulation in Culture of <I>Propionibacterium acnes </I> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4521</link>
<description><![CDATA[The Gram-positive skin bacterium <I>Propionibacterium acnes</I> was grown semi-anaerobically on Eagle\'s medium for 16 days at pH 6.7. Porphyrins were produced and accumulated in culture-grown P. acnes. Fluorescence spectroscopy was used to identify and quantify the amount of porphyrins produced in culture during the growth of the cells. Free base protoporphyrin IX (PPIX) as well as both free base coproporphyrin III (CPIII) and metallocoproporphyrin III (MCPIII) were identified in the culture. The CPIII was the dominant porphyrin species present in the early cultured-cells, however, the production and accumulation of PPIX was found to increase linearly with the age of the culture, which could be used in estimating the age of the culture of <I>P. acnes</I>. This investigation might help to understand efficient photodynamic therapy (PDT) of P. acnes. 
 ]]></description>
<dc:creator>M. Idrish Miah </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Spectroscopic Study of Porphyrin Production and Accumulation in Culture of <I>Propionibacterium acnes </I> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>27</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>21</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4522">
<title><![CDATA[Histochemical and Physicochemical Study of Bacterial Exopolysaccharides  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4522</link>
<description><![CDATA[Present study shows the complexity of determining the chemical composition of three exopolysaccharides obtained from bacteria associated with plant roots grown under salt stress conditions. Physicochemical analysis indicated that the exopolysaccharides were varying in their chemical composition. Presence of the sugar shows that these were hetero/homo polysaccharides. IR analysis of the crude extracts for the presence of functional groups indicated a need for more purification of exopolysaccharides. Moreover the IR analysis along with histochemical studies showed the presence of hydroxyl, carboxyl and nitro groups. The physicochemical characteristics of the exopolysaccharides showed that the exopolysaccharides would be used in industrial applications. However, a thorough investigation is needed to determine their industrial application. 
 ]]></description>
<dc:creator>Aamira Iqbal, Haq Nawaz Bhatti, Sofia Nosheen, Amer Jamil and Muhammad Ashraf Malik </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Histochemical and Physicochemical Study of Bacterial Exopolysaccharides  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>33</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>28</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4523">
<title><![CDATA[Production of Amyloglucosidase by UV Irradiated Strain of <I>Aspergillus niger</I> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4523</link>
<description><![CDATA[The parental strain of <I>Aspergillus niger </I>was subjected to UV irradiations for 5-30 minutes. One hundred and ten mutants of <I>Aspergillus niger </I>were isolated by observing the hydrolysis of starch in the petri plates. Of all the mutants tested, the mutant strain of <I>Aspergillus niger </I> GCBU-25, isolated after 25 minutes of UV irradiation gave the maximum production of AMG (136.1 IU/ml/min), which gave two fold increase in the production of the enzyme than the parental strain. The production of amyloglucosidase reached its maximum (183 IU/ml/min) when starch at 1% level and (NH<sub>4<sub>)<sub>2</sub>SO<sub>4</sub> at 0.2% level of nitrogen was used as carbon and nitrogen source respectively.
 ]]></description>
<dc:creator>Ikram-ul-Haq, Shahida Javed and Hamad Ashraf </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Production of Amyloglucosidase by UV Irradiated Strain of <I>Aspergillus niger</I> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>39</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>34</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4524">
<title><![CDATA[Effect of Different Mineral Nutrients on Invertase Production by Saccharomyces cerevisiae GCB-K5  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4524</link>
<description><![CDATA[The effect of different mineral nutrients was studied on the production of extracellular invertases by <I>Saccharomyces cerevisiae</I> GCB-K5. Nutritional studies were carried out in 250ml Erlenmeyer flasks by submerged fermentation. The culture medium (pH 6.0) was incubated for 48 hours at 30<sup>o</sup>C. The optimum levels of peptone and dipotassium hydrogen phosphate were found to be 4.0 and 0.2 g/l, respectively. Maximum invertase activity was found to be 12.68 U/ml. The amount of sugar consumed and dry cell mass were 21.08 and 5.88g/l, respectively. 
 ]]></description>
<dc:creator>Kiran Shafiq, Sikander Ali and Ikram-ul-Haq </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Effect of Different Mineral Nutrients on Invertase Production by Saccharomyces cerevisiae GCB-K5  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>44</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>40</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4525">
<title><![CDATA[Chemical Composition and Antimicrobial Activity of Essential Oil of <I>Salvia verbenaca </I> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4525</link>
<description><![CDATA[The aerial parts of <I>Salvia verbenaca </I>L. (Labiatae) afforded an essential oil on steam distillation was analyzed by gas chromatography-mass spectrometry (GC/MS) using direct injection. Out of fifty-two peaks (representing 99.2% of the oil), forty-one components were identified representing 96.3% of the total oil composition. The major components were sabinene (16.0%), d-cadinene (7.9%), -pinene (7.3%), 4-terpeniol (7.4%) and limonene (6.7%). The oil was also screened for its anti-microbial activity, which exhibited a significant anti-bacterial activity against <I>Bacillus subtilis, Staphylococcus aureus </I>and <I>Mycobacterium smegmatis</I>, and a marked anti-fungal activity against <I>Candida albicans</I>.
 ]]></description>
<dc:creator>Tawfeq A. Al-Howiriny </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Chemical Composition and Antimicrobial Activity of Essential Oil of <I>Salvia verbenaca </I> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>48</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>45</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4526">
<title><![CDATA[Effect of Media, Growth Regulators and Genotypes on Callus Induction and Regeneration in Wheat (<I>Triticum estivum</I>) ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4526</link>
<description><![CDATA[Effects of media, growth regulators and genotype were investigated for callus induction, maintenance and regeneration in wheat (<I>Triticum aestivum</I> L. cvs., Chakwal 86, Rawal 87). The percentage of callus induction in Rawal 87 was 49.58 -75.62% on Murashige and Skoog (MS) medium and 58.31-91.58% on N6 medium. For Chakwal-86, callus induction frequency ranged from 52.08- 81.04% on MS medium and 53.12- 81.02% on N6 medium supplemented with 2mg/l 2, 4 dichlorophenoxy acetic acid(2,4-D) singly, and with three concentrations (0.1, 0.5 and 1mg/L) of 6-Benzylaminopurine (BAP). BAP proved to play no role in callus induction. Sorbitol promoted callus proliferation, on N6 medium supplemented with 2mg/L 2,4-D. For plant regeneration from calli, MS medium with 0.1mg/L IAA and four concentrations (0.5, 1.0, 2.5 and 5mg/L) of BAP were tested. Regeneration frequency was greater (31.9%) in Rawal 87 on the medium containing 0.5mg/L BAP whereas 2.5mg/L of BAP were found suitable for regeneration in Chakwal 86 (15.27%).
]]></description>
<dc:creator>Hamid Rashid, Rizwana Abdul Ghani and Zubeda Chaudhry</dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Effect of Media, Growth Regulators and Genotypes on Callus Induction and Regeneration in Wheat (<I>Triticum estivum</I>) ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>54</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>49</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4527">
<title><![CDATA[Antibacterial Activity of Hydrodistilled Essential Oil of <I>Psammogeton canescens </I>N.O. Umbelliferae  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=97&amp;articleno=4527</link>
<description><![CDATA[The essential oil of <I>Psammogeton canescens </I> obtained by hydrodistillation was evaluated for its antibacterial activity against gram positive (<I>Bacillus megaterium, B. subtilis, Lactobacillus acidophilus, Micrococcus leuteus, Staphyllococcus albus, S.aureus, Vibrio cholera</I>) and gram negetive bacteria (<I>E. coli, Salmonella typhae, Shigella ferrarie</I>). The oil was found active against all the bacterial strains. However the activity of oil varies with its concentration and kind of bacteria. The oil showed activity even at 50g concentration. The antibacterial activity was comparable with amoxil, streptomycin and kanamycin. The oil had bactericidal activity against all the bacteria under investigation except <I>Shigella ferrarie, Micrococcus leuteus </I> and <I>Vibrio cholera</I>. The MIC value of oil varies from 75.5-160 and 75.5-135 mg per mL against gram positive and gram negetive bacteria, respectively. 
 ]]></description>
<dc:creator>Mujeeb ur Rahman and Shereen Gul </dc:creator>
<dc:date>2002-01-01</dc:date>
<dc:title><![CDATA[Antibacterial Activity of Hydrodistilled Essential Oil of <I>Psammogeton canescens </I>N.O. Umbelliferae  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>60</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>55</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4528">
<title><![CDATA[Isolation and Screening of Fungi for the Biosynthesis of Alpha Amylase  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4528</link>
<description><![CDATA[This study is concerned with the isolation and screening of mould cultures for the biosynthesis of alpha amylase. Forty mould culture were isolated from soil and tested for the production of alpha amylase. Of all the culture tested, the Saccharomyces cerevisiae-20 and <I>Aspergillus niger</I>-34 gave maximum production of alpha amylase. These strains were tested for the screening of culture media and M1 containing yeast extract, peptone, soluble starch ammonium sulphate, CaCl<sub>2</sub>, MgSO<sub>4</sub>, FeSO<sub>4</sub> in 100 ml of phosphate buffer gave maximum 2 4 4 production of alpha amylase by <I>Saccharomyces cerevisiae</I>. However, <I>Aspergillus niger</I>-34 gave insignificant result. Thus, Saccharomyces cerevisiae -20 was selected for the production of alpha amylase. The production of alpha amylase was reached optimum 72 h after inoculation at pH 5.5.
 ]]></description>
<dc:creator>Ikram-ul-Haq, Roheena Abdullah, Hamad Ashraf and Athar Hussain Shah </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[Isolation and Screening of Fungi for the Biosynthesis of Alpha Amylase  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>66</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>61</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4529">
<title><![CDATA[In vitro Shoot Tip Culture of Sugar-cane (<I>Saccharum officinarum</I>) Variety Isd 28  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4529</link>
<description><![CDATA[Multiple shoots were obtained from shoot tip explant of sugar-cane (<I>Saccharum officinarum</I>) cultured on MS medium supplemented with BAP (0.5-2.0 mg l<sup>-1</sup>), Kn (0.1-0.5 mg l<sup>-1</sup>) and IBA (0.1-0.5 mg l<sup>-1</sup>). Roots were induced in in vitro regenerated shoots on half MS medium supplemented with 5.0 mg l<sup>-1</sup> NAA, IBA and IAA. Plant regeneration from shoot tip was the highest on MS medium supplemented with BAP 2.0 mg l<sup>-1</sup> and IBA 0.5 mg l<sup>-1</sup>. The reported experimental findings present a method of plant regeneration of sugar-cane variety Isd 28 through shoot tip culture. The plantlets were successfully transferred to soil and the percentage of survivability under <I>ex vitro </I> condition was 70.
 ]]></description>
<dc:creator>R. Baksha, R. Alam, M.Z. Karim, S.K. Paul, M.A. Hossain, M.A.S. Miah and A.B.M.M. Rahman  </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[In vitro Shoot Tip Culture of Sugar-cane (<I>Saccharum officinarum</I>) Variety Isd 28  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>72</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>67</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4530">
<title><![CDATA[<I>In vitro </I>Effect of Salt on the Vigor of Potato (<I>Solanum tuberosm</I> L.) Plantlets  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4530</link>
<description><![CDATA[The effects of NaCl stress on in vitro induced potato plantlets of variety of potato <I>Solanum tuberosm </I>L.) commercial variety cardinal was studied at Potato Research Center, Abbottabad, NWFP, Pakistan. Five NaCl treatments, each consisting of 0, 1, 2, 3 and 4% were used. Viability percentage, fresh weight of plantlet and height of plantlet was decreased by given range levels of NaCl. The effect of all treatments was very drastic on length of roots and number of roots per plantlet where no response was recorded. The treatment of 4% NaCl depressed all the parameters understudy. The results indicate that the variety "Cardinal" is not salt tolerant, even at 1% salt concentration.
 ]]></description>
<dc:creator>Farhatullah, Rashid Mahmood and Raziuddin </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[<I>In vitro </I>Effect of Salt on the Vigor of Potato (<I>Solanum tuberosm</I> L.) Plantlets  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>77</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>73</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4531">
<title><![CDATA[Evolution of Genomes and Genome Relationship among the Rapeseed and Mustard  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4531</link>
<description><![CDATA[Reports regarding the chromosomal architecture of <I>Brassica genomes</I> and genome relationship among various species of the genus appeared in the second quarter of the 20th century AD. In the second quarter genome relationship was elaborated through secondary associations, pachytene and somatic karyotypes. Genome analysis and preferential pairing were extensively utilized for characterizing <I>Brassica genomes </I>in the third quarter. In last quarter of the century molecular characterization supplemented the conventional analytical tools for understanding the infrastructure of Brassica genomes. Whether it is the breeding system analysis, chromosome morphology, meiotic associations or molecular characterization proves that Brassica is monophyletic origin and it descended from an unknown six chromosomal prototype. Scientific developments made in Brassica genetics, from genome analysis to genomics during the 20th century AD are generalized in this paper. 
 ]]></description>
<dc:creator>Habib Ahmad, Shahida Hasnain and Afzal Khan </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[Evolution of Genomes and Genome Relationship among the Rapeseed and Mustard  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>87</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>78</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4532">
<title><![CDATA[Sub-acute Toxicity Studies of a Metabolite of <I>Streptomyces</I> Species  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4532</link>
<description><![CDATA[The ethyl acetate extract of yeast extract-glucose broth medium of an Actinomycetes strain, Streptomyces yielded a reddish yellow metabolite by chromatographic technique and was identified as 2-N-butanamide-3-methyl-4-methoxy-5--L-arabinosyl-propanophenone (MZ-4) on the basis of spectral data. The sub-acute toxicity study of this metabolite was carried out on long Evan\'s rats. The change of haematological and biochemical parameters were statistically insignificant. No abnormalities were found in the histopathology of the liver, kidneys, heart, lungs and spleen in the experimental group of rats at a dose of 300 g rat<sup>-1</sup> day<sup>-1</sup> for 14 consecutive days, when compared with the control group. 
 ]]></description>
<dc:creator>M. Zakir Sultan, Z. Sultana Sathi, M. Shah Alam Bhuiyan, M. Akteruzzaman Choudury, M. Helal Uddin Biswas, M.A. Gafur and M. Aziz Abdur Rahman </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[Sub-acute Toxicity Studies of a Metabolite of <I>Streptomyces</I> Species  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>93</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>88</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4533">
<title><![CDATA[Toxicity Study of 8-Propionato-2- (D+) Glucosyl-9, 10-Pyranopyridine Isolated from <I>Streptomyces</I> species on Long Evan`s Rats ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4533</link>
<description><![CDATA[The subacute toxicity studies of 8-propionato-2- (D+) glucosyl-9, 10-pyranopyridine (R-1), isolated from the <I>Streptomyces</I> species was carried out in Long Evan\'s rats. The compound was administered at a dose of 300 g/rat/day for 14 consecutive days. The gross general observations such as changes of body weight, hematological profiles, biochemical parameters of blood and the histopathology of the liver, kidney, heart and lungs were investigated both in control and experimental rats. The body weights of the rats were slightly increased. The change of hematological and biochemical parameters were statistically nonsignificant. No abnormalities were detected in the histopathology of the liver, kidneys, heart and lungs in the experimental group of rats as compared with control group of rats.
]]></description>
<dc:creator>Ranjan Kumar Barman, Zakia Sultana Sathi, M. Anwar Habib, M. Aktar Uzzaman Chowdhury, M. Helal Uddin Biswas, M.A. Gafur and M. Aziz Abdur Rahman</dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[Toxicity Study of 8-Propionato-2- (D+) Glucosyl-9, 10-Pyranopyridine Isolated from <I>Streptomyces</I> species on Long Evan`s Rats ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>99</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>94</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4534">
<title><![CDATA[<I>In vitro</I> Antibacterial Activity of an Active Metabolite Isolated from <I>Streptomyces </I>Species  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4534</link>
<description><![CDATA[The ethyl acetate extract of yeast extract-glucose broth medium of an Actinomycetes strain, Streptomyces yielded a reddish yellow antibiotic metabolite by chromatographic technique and was identified as 2 N-butanamide 3-methyl 4-methoxy 5--L-arabinosyl propanophenone (MZ-4) on the basis of spectral data. The compound exhibited significant antibacterial activity against five gram positive and nine gram negative bacteria when compared with standard Kanamycin antibiotic. The zone of inhibition were observed between 17 to 20 mm. The minimum inhibitory concentration (MIC) of the compound was determined against four gram positive and gram negative bacteria and the values were found between 32 and 64 g ml<sup>-1</sup>. 
 ]]></description>
<dc:creator>M. Zakir Sultan, Naznin Ara Khatune, Zakia Sultana Sathi, Md. Shah Alam Bhuiyan, M. Golam Sadik, M. Akteruzzaman Choudury, M. A. Gafur and Md. Aziz Abdur Rahman </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[<I>In vitro</I> Antibacterial Activity of an Active Metabolite Isolated from <I>Streptomyces </I>Species  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>107</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>100</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4535">
<title><![CDATA[Temperature Optima for Citric Acid Accumulation by <I>Aspergillus niger </I> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4535</link>
<description><![CDATA[The effect of different temperatures on citric acid fermentation by <I>Aspergillus niger </I> ANABt was studied in a 15 L stirred fermentor. Ferrocyanide treated (200 ppm) cane molasses medium containing sugar 150 g l<sup>-1</sup>, was used as the basal fermentation medium. The citric acid yield ranged from 48.58-65.96 g l<sup>-1</sup>. Maximum amount of anhydrous citric acid obtained during the course of study was 65.96 g l<sup>-1</sup> at 30C. The sugar consumption was 98 g l<sup>-1</sup> while mycelial dry weight was 14.55 g l<sup>-1</sup>. Mycelia were intermediate round pellets.
 ]]></description>
<dc:creator>Asad-ur-Rehman, Sikander Ali and Ikram-ul-Haq </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[Temperature Optima for Citric Acid Accumulation by <I>Aspergillus niger </I> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>110</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>108</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4536">
<title><![CDATA[In vitro Seed Propagation of Dendrobium (Dendrobium transparens) Orchid as Influenced by Different Media  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4536</link>
<description><![CDATA[Four different media namely- Hyponex, Murashige and Skoog (MS), OKF1 and Knudson C (KC), were tested for large scale multiplication of sympodial native orchid, Dendrobium transparens Wall. via seeds. MS medium was found to be best for characters studied in Dendrobium transparens, followed by Hyponex medium but OKF1 medium gave the least performance. Days required to seed germination was the minimum (50 days) in MS medium while the maximum days (59 days) was required by OKF1 medium. Considering other characteristics, such as days required to protocorm formation and plantlet development, number of leaves and roots per plantlet, plantlet height and root length and finally plant survivability percentage, MS medium showed significantly better performance for in vitro seed propagation of Dendrobium transparens. 
 ]]></description>
<dc:creator>M.K. Alam, M.H. Rashid, M.S. Hossain, M.A. Salam and M.A. Rouf </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[In vitro Seed Propagation of Dendrobium (Dendrobium transparens) Orchid as Influenced by Different Media  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>115</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>111</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4537">
<title><![CDATA[Sub-acute Toxicity Study of 3,6-Dimethyl-4-Ethyl-O-Acetyl Benzene Isolated from Soil Streptomyces Species  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=98&amp;articleno=4537</link>
<description><![CDATA[The sub-acute toxicity study of 3,6-dimethyl-4-ethyl-0-acetyl benzene (BM-5), was carried out on Long Evan\'s rats using daily administration (300 g/rat/day) of compound for 14 consecutive days. Non-significant differences between weight of compound receiving rats and control rats (480.816 vs 460.816) were found. The change in hematological parameters was found to be nonsignificant (total count of RBC, 5.10.081 vs 4.630.094; white blood cell, 7.330.124 vs 5.730.124; platelets, 36166610274 vs 2616668498, (cell/ml) 106; percentage of hemoglobin 65.671.60 vs 560.816; ESR, 250.816 vs 19.670.471 for experimental and control rats, respectively) and biochemical parameters (serum glutamate pyruvate transaminase, 8.50.408 vs 8.33 0.471 IU L<sup>-1</sup>; serum glutamate oxaloacetate transaminase, 9.830.235 vs 9.330.234 IU L<sup>-1</sup>; bilirubin, 0.360.104 vs 0.340.016 g dL<sup>-1</sup>; creatinine, 0.67 0.089 vs 0.610.009 mg dL<sup>-1</sup>; urea, 18.830.235 vs 18.50.408 mg dL<sup>-1</sup>; for experimental and control rats). Therefore, the changes in body weight, hematological and biochemical parameters were statistically non-significant. No detectable abnormalities were found in histopathology of heart, kidney, liver and lung in experimental group of rats as compared with that of the control group of rats.
 ]]></description>
<dc:creator>Bytul M. Rahman, M.S.A. Bhuiyan, M. Golam Sadik and A.S.M. Anisuzzman </dc:creator>
<dc:date>2002-07-01</dc:date>
<dc:title><![CDATA[Sub-acute Toxicity Study of 3,6-Dimethyl-4-Ethyl-O-Acetyl Benzene Isolated from Soil Streptomyces Species  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>1</prism:volume>
<prism:endingPage>120</prism:endingPage>
<prism:publicationDate>2002</prism:publicationDate>
<prism:startingPage>116</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4538">
<title><![CDATA[Optimization of Various Parameters for the Production of Glucose Oxidase from Rice Polishing Using <I>Aspergillus niger</I> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4538</link>
<description><![CDATA[The enzyme glucose oxidase was produced by fermentation technology, using <I>Aspergillus niger</I> as fermentation organism and rice polishing as substrate. Maximum production of enzyme (3.42 U mL 1) was recovered at substrate level of 2% after 36 h of submerged fermentation. The pH for the optimal production of enzyme was found to be 4. Addition of salts such as urea (0.3%), CaCO<sub>3</sub> (0.04%) and KH<sub>2</sub>PO<sub>4</sub> (0.6%) into the fermentation medium enhanced enzyme production while MgSO<sub>4</sub>.7H<sub>2</sub>O was found to inhabit microbial growth and glucose oxidase production by <I>A. niger</I>. 
 ]]></description>
<dc:creator>Hafiz M. Hamid, Khalil-ur-Rehman, M. Anjum Zia and M. Asgher </dc:creator>
<dc:date>2003-01-01</dc:date>
<dc:title><![CDATA[Optimization of Various Parameters for the Production of Glucose Oxidase from Rice Polishing Using <I>Aspergillus niger</I> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>7</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>1</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4539">
<title><![CDATA[Bio-ethanol Fermentation by the Bioconversion of Sugar from Dates by <I>Saccharomyces cerevisiae </I>Strains ASN-3 and HA-4 ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4539</link>
<description><![CDATA[The essence of bioconversion of sugar containing materials by the use of screened microbial source is the significant need of today. Saccharomyces cerevisiae is one of the common and the cheapest source of bioconversion of substrate to the higher yield of bioethanol under the controlled optimization parameters. In the present study Saccharomyces cerevisiae strains ASN-3 and HA-4 were activated and finally used for ethanol fermentation from Dates. The results revealed that both strains are actively involved in fermentation process but it is concluded that strain HA-4 resulted higher cellular mass when inoculated in Malt Yeast extract Peptone Glucose medium supplemented with fructose and yeast nitrogen base and higher yield of ethanol was also observed when the activated strain were inoculated in dates syrup as substrate at 120 rpm, having pH 4.5 at 30C at 600 nm after 72 h post incubation. ]]></description>
<dc:creator>A.A. Noor, A. Hameed, Kouser Parveen Bhatti and Sarfraz A. Tunio </dc:creator>
<dc:date>2003-01-01</dc:date>
<dc:title><![CDATA[Bio-ethanol Fermentation by the Bioconversion of Sugar from Dates by <I>Saccharomyces cerevisiae </I>Strains ASN-3 and HA-4 ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>17</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>8</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4540">
<title><![CDATA[Isolation and Screening of Amino Acids Producing Bacteria from Milk ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4540</link>
<description><![CDATA[Twenty eight strains from buffalo and cow milk were tested for amino acids production in M-1, M-II and L-6 media, fourteen being from each source. Generally, bacterial strains did not produce significant amount of all amino acids, but bacteria from both sources produced aspartic acid and alanine in molasses media (M-I and M-II). Maximum production of aspartic acid (1.9 g L<sup>-1</sup>) was given by MB-7 and MB-12 in M-I medium after 72 h of fermentation. Some strains of both the sources also produced glutamic acid. Valine (maximum 1.4 g L<sup>-1</sup> by MC-10) was produced in M-I medium by some bacterial strains isolated from cow\'s milk only. In L-6 medium, lysine (maximum 1.8 g L<sup>-1</sup> by MB-6 and MC-13) was produced by all the isolates of both sources. The other amino acid which was produced in L-6 medium by majority of strains was isoleucine (maximum 2.1 g L<sup>-1</sup> by MB-6). MB-5 isolated from buffalo milk was found as the best strain in L-6 medium and its produced glutamic acid, lysine and alanine as 4.5, 1.3 and 5.1 g L<sup>-1</sup>, respectively. It was observed that bacterial strains isolated from buffalo milk were more productive than the strains obtained from cow milk. The strains MB-1, MB-5, MB-13 and MB-14 obtained from buffalo milk and MC-1, MC-7 and MC-13 from cow milk were selected as good amino acids producers strains. Thus aspartic acid, alanine, glutamic acid, lysine and isoleucine were the major amino acids produced from the bacterial strains of both the milk sources. ]]></description>
<dc:creator>Babar Hassan, M. Asghar, S. Nadeem, H. Zubair, H.M. Muzammil and M. Shahid </dc:creator>
<dc:date>2003-01-01</dc:date>
<dc:title><![CDATA[Isolation and Screening of Amino Acids Producing Bacteria from Milk ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>29</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>18</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4541">
<title><![CDATA[Production of Proteases by a Locally Isolated Mould Culture under Lab Conditions ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4541</link>
<description><![CDATA[Thirteen mould cultures, capable of producing proteases by solid state fermentation, were isolated from soil. <I>Rhizopus oligosporus</I> IHS<sup>13</sup> strain was found to be the best producer of acidic proteases. The agricultural by-products namely sunflower meal, wheat bran, soybean meal, lupin cake and cotton seed meal were evaluated as inducers for the production of enzyme. The enzyme synthesis was maximum when sunflower meal was used as substrate. The production of proteases by <I>Rhizopus oligosporus</I> HIS<sub>13<sub> strain was studied by varying the size of inoculum and type of diluent. The optimum inoculum size and diluent were 10% and distilled water, respectively. The effect of different buffers on the extraction of enzyme was also studied and distilled water was found to be the best extractor. The maximum enzyme production, obtained during the course of study was 4.8 U ml<sup>-1<sup>.
 ]]></description>
<dc:creator>Ikram-ul-Haq, Hamid Mukhtar, Sunila Daudi, Sikander Ali and M. A. Qadeer  </dc:creator>
<dc:date>2003-01-01</dc:date>
<dc:title><![CDATA[Production of Proteases by a Locally Isolated Mould Culture under Lab Conditions ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>36</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>30</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4542">
<title><![CDATA[Influence of ABA, Gibberellin and Kinetin on IAA Induced Adventitious Root Development on Hypocotyl Cuttings of Mungbean ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4542</link>
<description><![CDATA[GA<sub>3</sub> dissolved in 0.2% ethanol inhibited the adventitious root formation in mungbean cuttings. Conversely, when it is dissolved in water, GA<sub>3</sub> promoted the adventitious rooting response at 10<sup>-7</sup> and 10<sup>-8</sup> M concentrations. Ethanol suppressed the promoting effects of GA<sub>3</sub>. Generally, it has been observed that low concentration of GA<sub>3</sub>, favour rooting and high concentration inhibit it. Furthermore no evidence of synergism between supplied GA<sub>3</sub> and IAA was observed. Kinetin, at low concentration and in the presence of IAA promoted rooting response. ABA at 10<sup>-5</sup> M and in the presence of IAA promoted adventitious root formation. The stimulatory effects of ABA was more pronounced at 5x10<sup>-4</sup> concentration of ABA. ]]></description>
<dc:creator>Shamsa Yasmin, Basir Ahmed and Rashida Soomro </dc:creator>
<dc:date>2003-01-01</dc:date>
<dc:title><![CDATA[Influence of ABA, Gibberellin and Kinetin on IAA Induced Adventitious Root Development on Hypocotyl Cuttings of Mungbean ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>43</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>37</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4543">
<title><![CDATA[Influence of Genotypes on Plant Regeneration from Cotyledons of <I>Corchorus capsularis</I> L. ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4543</link>
<description><![CDATA[The present study was conducted on influence of genotypes on plant regeneration from cotyledons of <I>Corchorus capsularis</I> L. Multiple shoots were produced at the cut end of the petioles of each cotyledon of <I>C. capsularis <I>varieties on MS agar solidified medium supplemented by IAA and BAP. The results indicated that percentage of shoot regeneration from the cotyledon explants were found dependent on the genotypes used. Variation was observed among the varieties in number of cotyledons produced shoots and in number of shoots produced by each cotyledon. The highest number of shoots produced by each cotyledon and the highest number of cotyledons responded for shoot regeneration was recorded from Tri-cap-2. However, jute varieties have shown differences in  in vitro responses and the differences were statistically significant. The results showed that the regenerated plants from all varieties were rooted in vitro and successfully transferred in pots containing soil. The plants grew well into maturity and produced seeds. ]]></description>
<dc:creator>Zabun Naher, Asma Khatun, Sherin Mahbub, Md. Abdul Alim and Abu Bakar Siddique </dc:creator>
<dc:date>2003-01-01</dc:date>
<dc:title><![CDATA[Influence of Genotypes on Plant Regeneration from Cotyledons of <I>Corchorus capsularis</I> L. ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>51</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>44</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4544">
<title><![CDATA[Biotechnology: Promethean Science or Obsession? ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=99&amp;articleno=4544</link>
<description><![CDATA[Not Available ]]></description>
<dc:creator>S. Farooq and F. Azam </dc:creator>
<dc:date>2003-01-01</dc:date>
<dc:title><![CDATA[Biotechnology: Promethean Science or Obsession? ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>72</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>52</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4545">
<title><![CDATA[Isolation and Characterization of 2,4-Dichlorophenoxyacetic Acid Degrading Organisms from Soil in Jordan Valley ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4545</link>
<description><![CDATA[2,4-Dichlorophenoxyacetic acid (2,4-D) degrading bacteria were isolated from soil samples collected from selected sites in Jordan Valley, which had a history of 2,4-D exposure. The herbicide 2,4-D was used in aminimal salt medium as a sole source of carbon to isolate and enumerate the 2,4-D-degraders by most probable  number (MPN) method. One site have previous history of exposure to 2,4-D found to contain 88 2,4-D-degraders/g soil suspension; other sites were not exposed to 2,4-D and showed much lower numbers of 2,4-D-degraders ranging from 0.5-2.1 degraders/g soil suspension. One of the 7 isolates was found to degrade 2,4-D entirely in 45 h and it was the most potent isolate. It was identified and found to be <I>Pseudomonas putida</I>. It grew and degraded 500 ppm of 2,4-D optimally at pH 6.5 and 30C. ]]></description>
<dc:creator>Amjad B. Khalil </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Isolation and Characterization of 2,4-Dichlorophenoxyacetic Acid Degrading Organisms from Soil in Jordan Valley ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>85</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>73</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4546">
<title><![CDATA[An Efficient Protocol for Plant Regeneration from the Cotyledons of Kenaf (<I>Hibiscus cannabinus</I> L.)]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4546</link>
<description><![CDATA[Plant regeneration was obtained from the cotyledonary petioles of kenaf (<i>Hibiscus cannabinus </i>L. var. HC-2) on MS medium supplemented by different levels of IAA or NAA and BAP. The effects of non-ionic surfactant, Pluronic F-68 have been studied on shoot regeneration of kenaf cotyledons with attached petioles in vitro. The effect was most marked in 0.1% and 0.5% level of Pluronic F-68 in addition to usual plant regeneration medium. These results were found significantly much higher than the control. The difference between control and Surfactant-treated cotyledons was marked. Plants regenerated from the Pluronic-treated cotyledons were found morphologically normal. Pluronic F-68 has been proved to be a growth stimulating agent for increasing the shoot regeneration efficiency of kenaf explants and this system can used for other crop plants.
]]></description>
<dc:creator>Khatun A., Zabun Naher, Shirin Mahboob, Chandan Kumar Saha and Shana Bilkis</dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[An Efficient Protocol for Plant Regeneration from the Cotyledons of Kenaf (<I>Hibiscus cannabinus</I> L.)]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>93</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>86</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4547">
<title><![CDATA[Effect of Coliphage Entrapment on its Interaction with the Host Bacterium  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4547</link>
<description><![CDATA[Coliphage isolate CPS1 was entrapped in different gel matrices to simulate the entrapment of enteric viruses in natural biofilms. K-Carrageenan beads at 2% concentration allowed the release of phage particles enough to cause more decrease in the growth rate of the host bacterium. Alginate beads allowed a slower rate of release of phages. Sequential release in successive recycles of the phage-seeded beads still decreased effectively the growth rate of E. coli (13706). Addition of phage seeded beads into sewage water significantly decreased the estimates of faecal coliforms in the water sample. ]]></description>
<dc:creator>Faiza A. Fattouh, Samy A. EL Aassar, Aida E.M. Farag  and Sahar W. Hassan </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Effect of Coliphage Entrapment on its Interaction with the Host Bacterium  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>100</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>94</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4548">
<title><![CDATA[Studies on Multiple Antibiotic Resistance Gene in <i>Aeromonas</I> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4548</link>
<description><![CDATA[Three xylanase-producing Aeromonas strains (St<sub>1</sub>, So<sub>1</sub> and So<sub>2</sub>) were isolated from stagnant water from Rajshahi University campus. The strains were isolated on xylan agar media and screened by  -xylanolysis method. This strains showed drug resistance to cotrimoxazole, ampicilline and amoxycilline when tested by disc diffusion method on nutrient agar or xylan agar plate respectively. This strains also showed sensitive to erythromycin, tetracycline and doxycyclin. The minimum inhibitory concentration (MIC) of erythromycin, tetracycline and doxycyclin was determined by serial dilution technique against three test bacterial strains. The MIC values of the above three drugs against St<sub>1</sub> were 250, 125 and 250 g ml<sup>-1<sup>, against So<sub>1</sub> and So<sub>2</sub> were 125, 62.5 and 125 g ml<sup>-1</sup> respectively. Plasmid DNA was isolated the multi-drug resistant strain St<sub>1</sub>. These drug resistant plasmids were transformed into sensitive <I>E. coli</I> LE 392. The transformed LE392 became resistant to cotrimoxazole, ampicilline and amoxycilline and the respective plasmid DNA was detected in the plasmid DNA isolated from transformed <I>E. coli</I> cells. The antibiotic resistant in Aeromonas was plasmid born. ]]></description>
<dc:creator>Narayan Roy Md Belaluddin and M. Shahjahan </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Studies on Multiple Antibiotic Resistance Gene in <i>Aeromonas</I> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>108</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>101</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4549">
<title><![CDATA[Purification of Mutarotase, Extracted from Bovine Kidney Cortex ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4549</link>
<description><![CDATA[Bovine kidney cortex was homogenized to extract mutarotase that was subjected to ammonium sulfate precipitation, ion exchange and gel filtration chromatographic techniques. The activity and specific activity of crude enzyme was observed as 1.27 and 0.34 U mg<sup>-1</sup>, respectively which was increased by 3.52 and 2.55 U mg<sup>-1</sup> after partial purification by ammonium sulfate precipitation and desalting. The enzyme was then subjected to DEAE column for ion exchange chromatography and the resultant activity and specific activity gained by the enzyme was 3.17 and 2.50 U mg<sup>-1</sup>, respectively. After gel filtration chromatography through sephadex G-150, the observed activity and specific activity was 2.894 and 3.36 U mg<sup>-1</sup> which indicates 9.97 fold purification. ]]></description>
<dc:creator>M. Anjum Zia, Khalil-ur-Rehman, Nadia Jamil and Farzana Alyas </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Purification of Mutarotase, Extracted from Bovine Kidney Cortex ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>114</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>109</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4550">
<title><![CDATA[<I>In vitro</I> Shoot Multiplication of <I>Chrysanthemum morifolium</I> as Affected by Sucrose, Agar and pH.]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4550</link>
<description><![CDATA[Effects of sucrose, agar and pH on in vitro shoot multiplication of Chrysanthemum were studied. Nodal explant from the ex vitro grown plant was used as the test material. For optimum shoot induction and multiplication in MS medium containing BAP+ sucrose 30 gm l<sup>-1</sup>, agar 6 gm l<sup>-1</sup> and pH 5.5-6.0 proved more effective. The media having 30 gm l<sup>-1</sup> sucrose showed the highest percentage of explant responded to shoot proliferation and that was 100%. This sucrose concentration also showed the optimum result for number of usable shoots per culture, number of node shoot 1 and average length of shoots and the values were 5.40.6, 5.10.8 and 5.60.4 cm. The highest proliferation response of the explant was observed on MS medium having 6 gm l<sup>-1</sup> of agar and the frequency was 100%. Among different level of pH, the highest percentage of explant showing proliferation was observed on the media adjusted to pH 5.5 and 6.0. The results presented here proved to be suitable for the <i>in vitro</i> shoot multiplication of <i>Chrysanthemum morifolium.</i>]]></description>
<dc:creator>M.Z. Karim, M.N. Amin, M.A.K. Azad, F. Begum, M.M. Rahman, S. Ahmad and R. Alam</dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[<I>In vitro</I> Shoot Multiplication of <I>Chrysanthemum morifolium</I> as Affected by Sucrose, Agar and pH.]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>120</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>115</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4551">
<title><![CDATA[Easy and Rapid Detection of Point Mutations in the Human  beta-hemoglobin Gene with DNA-chips ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4551</link>
<description><![CDATA[Study was conducted on hemoglobinopathies the world\'s most common class of single gene disorders. We selected four point mutations of the human  beta-hemoglobin gene, giving rise to frequently occurring unstable  beta-hemoglobin variants or  beta-thalassemias. Our chip system is based on allele-specific oligonucleotide hybridization to detect single nucleotide polymorphisms (SNPs) and mutations. The probes attached to the chip surface consist of oligonucleotides containing the point mutations and the three corresponding control sequences. The labeled target cDNAs used for hybridization are derived from genomic or subcloned genomic DNA via asymmetric PCR, which is specially adapted for the synthesis of labeled single stranded target DNA. In addition to the useage of a chip reader, evaluation of the hybridized chip is adapted for using enhanced chemiluminescence. With this chip all four hemoglobin point mutations are easily detected and furthermore, homozygous alleles are distinguished from heterozygous alleles. Our SNP chip system is ready for rapid detection of all point mutations and SNPs occurring in the hemoglobin and other genes. ]]></description>
<dc:creator>Joaquin Brintrup, Weidong Du, Flavio Ortigao, Marianne Krause, Klaus-Michael Debatin, Elisabeth Kohne and Hubert Hug </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Easy and Rapid Detection of Point Mutations in the Human  beta-hemoglobin Gene with DNA-chips ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>130</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>121</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4552">
<title><![CDATA[DNA-fingerprints and Phylogenetic Studies of Some Chitinolytic Actinomycete Isolates ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4552</link>
<description><![CDATA[Twenty-one chitinolytic actinomycete-isolates were isolated on chitin agar and were able to degrade chitin as sole carbon source. Total count of chitinolytic active actinomycetes (halo-forming colonies) were significantly lower (P<0.05) than those non-active colonies (non -halo-forming colonies). Rizosphere of <I>Alkanna orientalis</I> plants grown in Saint Catherine area was better habitat for chitinolytic actinomycetes than other rhizospheres of tested plants grown in Suez Canal farm. Using RAPD analysis in an attempt to generate specific markers for chitinolylic actinomycete-isolates, we able to analyzed seven randomly polymorphic DNA primers against the most active chitinolytic actinomycete-isolates. Most of the primers used were useful in identifying unique DNA polymorphisms of all isolates tested. Thirty RAPD-PCR markers were found to be effective to be used as isolate-specific markers. Phylogenetic relationships between the isolates using previous technique (RAPD analysis) revealed that the isolates with higher similarity percent were belong to the same taxonomical group. Using standard techniques of actinomycete identification, morphological and physiological characterization, strengthened these results. ]]></description>
<dc:creator>Zaki A. El-Fiky, Samira R. Mansour, Yahia El-Zawhary and Samar Ismail </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[DNA-fingerprints and Phylogenetic Studies of Some Chitinolytic Actinomycete Isolates ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>140</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>131</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4553">
<title><![CDATA[Whey Induced-Modifications in Growth, Photosynthetic Characteristics, Protein patterns and Water Relations of Wheat Seedlings ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4553</link>
<description><![CDATA[A pot experiment was conducted to investigate the effect of presoaking of wheat grains in cheese whey at different concentrations (0, 25, 50 and 100 %) on growth vigor of wheat seedlings and some physiological criteria. Whey treatment at 50% level induced a marked increase in shoot length, shoot fresh and dry masses and total leaf area of wheat plants as compared with control plants. On the other hand, the other used whey concentrations had no significant effect on the abovementioned criteria. In comparing to control plants, whey concentrations appeared to improve Hill activity and photosynthetic pigments and this effect depends mainly on the applied whey concentration. On the other hand, only 50% level of whey increased total 14C photoassimilates and consequently soluble and insoluble carbohydrate fractions of wheat plants as compared with control plants. Furthermore, this treatment induced noticeable increase in total carbohydrates and total nitrogen content of wheat seedlings. Qualitative and quantitative analysis of protein profile indicated that whey at 25 and 50 % levels increased protein concentrations in wheat seedlings and the effect was more elicited with 47- 89 kDa polypeptides. Moreover, all whey treatments induced new protein bands with molecular weight 5 and 33 kDa. Grain priming with 50% whey significantly increased K, Ca and P concentrations of wheat seedlings. Magnesium concentration appeared to increase in wheat with increasing whey concentration as compared with control plants. Total leaf conductivity and transpiration rate of wheat seedlings were increased in response to grain priming in cheese whey at 25 and 50% level. Conversely, whey treatment at 100% level appeared to reduce transpiration rate and total leaf conductivity. Relative water content (RWC) was greatly increased in wheat seedlings with whey treatments. ]]></description>
<dc:creator>S.A. Haroun and A.H. Ibrahim </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Whey Induced-Modifications in Growth, Photosynthetic Characteristics, Protein patterns and Water Relations of Wheat Seedlings ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>153</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>141</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4554">
<title><![CDATA[Somatic Embryogenesis and Plant Regeneration from Immature Embryo Derived Callus of Inbred Maize (<I>Zea mays</I> L.) ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4554</link>
<description><![CDATA[The present study was carried out to develop protocol in which plants could be regenerated with easy and in high numbers from tissue cultures of maize. The tissues of immature embryos were tested in three inbred lines (CML-161, CML-323, CML-327) MS and N6 were used. In N6 medium, the range of embryogenic calli formation was varied from 56.33-72.0%. The results indicated that the highest amount 72.0% was obtained when N6 was supplemented with L-proline 2.3 gm l<sup>-1</sup>, Casein Hydrolysate 200 mg l<sup>-1</sup> and 2,4-D 1.0 mg l<sup>-1</sup>. Where as in MS medium the embryogenic calli formation was varied from 39.0-68.66%. In this case the highest amount (68.66) was obtained where MS was supplemented with L-Asparagine 150 mg l 1, Thiamin 50 mg l<sup>-1</sup> and 2,4-D 1 mg l<sup>-1</sup>. Plants were regenerated successfully from embryogenic callus in hormone free MS medium. The results showed that MS (52.83-61.0%) medium was found better than N6 (35.66-42.49%). The mode of somatic embryogenesis was studied using histological technique.  ]]></description>
<dc:creator>A.M. Shohael, M.A.L. Akanda, S. Parvez, S. Mahfuja, M.F. Alam, R. Islam and N. Joarder  </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Somatic Embryogenesis and Plant Regeneration from Immature Embryo Derived Callus of Inbred Maize (<I>Zea mays</I> L.) ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>161</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>154</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4555">
<title><![CDATA[Phytohaemagglutinins in Membrane Signalling, Biomedical and Genetic Engineering Research ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=100&amp;articleno=4555</link>
<description><![CDATA[Plant lectins have long been used as powerful and specific tools in carbohydrate chemistry and histology. Lectins are now also recognized in their own right as a class of communication proteins which are involved in interactions between plants and their environment and may also have physiological functions within the plant. Using molecular modelling techniques, new opportunities have arisen to explore similarities, make predictions and establish correlations in sugar-binding activity and/or specificity between well-studied and newly discovered lectins. This paper attempts to review the major plant lectin family, their physiology, carbohydrate binding specificity, their role in biomedical and genetic engineering of crop plants, towards pests and disease resistance. ]]></description>
<dc:creator>C.N. Fokunang and R.A. Rastall </dc:creator>
<dc:date>2003-05-01</dc:date>
<dc:title><![CDATA[Phytohaemagglutinins in Membrane Signalling, Biomedical and Genetic Engineering Research ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>177</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>162</prism:startingPage>
</item>


<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4556">
<title><![CDATA[Selection of Fermentation for Citric Acid in Bioreactor ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4556</link>
<description><![CDATA[Twenty-five strains of <I>Aspergillus niger</I>, isolated from different soil samples were evaluated for citric acid production. Shake flask technique was employed for screening of the isolated. The best citric acid producing strain, GCB-14, was selected for further studies using a laboratory scale stirred fermentor. Cane-molasses medium and sucrose salt medium were tested for the basal fermentation medium. The results indicated that maximum amount of citric acid i.e. 55.43 gl<SUP>-1</SUP> was produced 144 h after incubation using cane-molasses medium. The maximum amount of sugar consumed and dry cell mass produced were 126 and 27.49 gl<SUP>-1</SUP>, respectively. Therefore, cane-molasses was optimized as the basal fermentation medium for maximal citric acid production. ]]></description>
<dc:creator>Asad-ur-Rehman, Sikander Ali and Ikram-ul-Haq </dc:creator>
<dc:date>2003-09-01</dc:date>
<dc:title><![CDATA[Selection of Fermentation for Citric Acid in Bioreactor ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>184</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>178</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4557">
<title><![CDATA[Isolation and Screening of <I>Aspergillus niger</I> Isolates for Xylanase Biosynthesis ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4557</link>
<description><![CDATA[Present investigation deals with the isolation and screening of <I>Aspergillus niger</I> isolates for the biosynthesis of xylanase. About 104 different strains of <I>Aspergillus niger</I> were isolated from soil collected from different areas of Lahore by serial dilution method on xylene agar malt extract medium. The strains with larger whitish zones of xylene hydrolysis were picked up and transferred to the PDA slants. The cultures were incubated at 30C for 3-5 days for maximal sporulation. The <I>Aspergillus niger</I> strains were screened for xylanase production by submerged fermentation. Xylanase activity was ranged from 30-225 
U ml<SUP>-1</SUP> and dry cell mass from 6.48-26.56 g 
L<SUP>-1</SUP>. Maximum xylanase productivity  was  obtained  by  GCBT-35  (225  U  
ml<SUP>-1</SUP>).  
The  mycelial  dry  weight  was 9.54 g L<SUP>-1</SUP> while mycelia were small in size and rounded in shape. ]]></description>
<dc:creator>Ayesha Khan, Ikram-ul-Haq, Waseem Ahmad Butt and Sikander Ali </dc:creator>
<dc:date>2003-09-01</dc:date>
<dc:title><![CDATA[Isolation and Screening of <I>Aspergillus niger</I> Isolates for Xylanase Biosynthesis ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>190</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>185</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4558">
<title><![CDATA[<I>In vitro</i> Response of Potato (<I>Solanum tuberosum</I> L.) to Various Growth Regulators  ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4558</link>
<description><![CDATA[The effect of three different growth regulators viz: Naphthalene Acetic Acid (NAA), Indole Acetic Acid (IAA) and Indole Butyric Acid (IBA) each at five concentration levels (0.0, 0.05, 0.15, 0.25 and 0.35) was evaluated on meristem culture of Potato (<I>Solanum tuberosum </I>L.) for production of virus-free plantlets. The parameters included were plantlet height, number of nodes/plantlet, number of leaves/plantlet, root length and number of roots/plantlet. Maximum plantlet height (9 cm) with NAA at 0.15 mg l<SUP>-1</SUP>, higher number of nodes/plantlet (9.714) with IBA at 0.35 mg l<SUP>-1</SUP> and maximum number of leaves/plantlet (6.143) with IAA at 0.25 mg l<SUP>-1</SUP> were recorded. ]]></description>
<dc:creator>Abdul Ghaffoor, Gul Bahar Shah and Kashif Waseem </dc:creator>
<dc:date>2003-09-01</dc:date>
<dc:title><![CDATA[<I>In vitro</i> Response of Potato (<I>Solanum tuberosum</I> L.) to Various Growth Regulators  ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>197</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>191</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4559">
<title><![CDATA[Growth Stimulatory Effects of <I>Azospirillum</I> Strains on <I>Triticum aestivum </I>and <I>Vigna radiata</i> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4559</link>
<description><![CDATA[Five bacterial strains of <I>Azospirillum</I> (As-2, As-4, As-5, As-6 and As-8) were used both as monocultures and mixed cultures (twenty-six combinations for each plant) for the inoculation of <I>Triticum aestivum </I>(non leguminous) and <I>Vigna radiata </I>(leguminous) seeds. Inoculated as well as non inoculated seeds were germinated and grown under controlled temperature and light conditions for 10 days. Growth parameters revealed that in both plants, mono culture inoculations manifested the better growth as compared to non inoculated treatments. Mixed cultures inoculation 3j (three strain combination) and 4a (four strain combination) in <I>T. aestivum</I> and 4a (four strain combination) and 3i (three strain combination) in <I>V. radiata</I> exhibited synergistic responses as compared to control treatment. Stimulatory effects were more pronounced in non leguminous seedlings relative to leguminous one. ]]></description>
<dc:creator>Amina Munir, Iram Munir, Shazia Afrasyab and Shahida Hasnain </dc:creator>
<dc:date>2003-09-01</dc:date>
<dc:title><![CDATA[Growth Stimulatory Effects of <I>Azospirillum</I> Strains on <I>Triticum aestivum </I>and <I>Vigna radiata</i> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>205</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>198</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4560">
<title><![CDATA[Plant Regeneration from the Cotyledonds of Tossa Jute (<I>Corchorus olitorius </I>L<I>.</I>) ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4560</link>
<description><![CDATA[Plant regeneration from the cotyledons of <I>C. olitorius</I> has recently been optimized at Bangladesh Jute Research Institute (BJRI). One of the major constraints of getting plant regeneration from the explants of <I>C. olitorius</I> was the production of healthy seedlings <I>in vitro</I>. An efficient seed germination system and healthy seedling production have been established at BJRI. Seeds of different varieties (O4, O9897, OM1 and O72) of <I>C. olitorius</I> germinated on both agar supported hormone free MS medium and cotton supported hormone free liquid MS medium. The percentage of seeds germinated on cotton supported medium was found to be much higher than seeds germinated on agar supported medium. This system ensured maximum of an average of 98% seed germination. Whereas, in case of agar-supported medium an average of 46% seeds could be germinated with very slow growth. The seedlings grown on cotton supported medium were found to be much more healthily than seedlings grown on agar supported medium. Plant regeneration was obtained from the cotyledonary petioles of the varieties (O4, O9897, OM1 and O72) of <I>C. olitorius</I> on MS agar solidified medium supplemented by IAA 0.5 and BAP 3.0 mg l<SUP>-1</SUP>. The efficiency of plant regeneration from the cotton supported seedlings was found to be as good as the agar supported seedlings. The plantlets produced roots on hormone free MS medium readily. After transfer to soil the plants grew into maturity and produced fruits. No morphological changes were noticed. ]]></description>
<dc:creator>Asma Khatun, Chandan Kumar Saha, Zabun Naher, Shirin Mahbub, Abu Bakar Siddique and Shahana Bilkis </dc:creator>
<dc:date>2003-09-01</dc:date>
<dc:title><![CDATA[Plant Regeneration from the Cotyledonds of Tossa Jute (<I>Corchorus olitorius </I>L<I>.</I>) ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>213</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>206</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4561">
<title><![CDATA[Effects of Plant Growth Regulators on Callus Proliferation, Plantlet Regeneration and Growth of Plantlets of <I>Doritaenopsis</I> Orchid ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4561</link>
<description><![CDATA[Supplement of 2,4-D and BAP into New <I>Phalaenopsis</I> (NP) medium was not effective for the growth of callus in <I>Doritaenopsis</I> orchid. Among the different combinations of BAP and NAA, 5.0 mg l<SUP>-1</SUP> BAP + 0.1 mg l<SUP>-1</SUP> NAA highly enhanced PLB formation from calli. For plantlet initiation from PLBs 0.5 mg l<SUP>-1</SUP> BAP was suitable and higher  concentration was inhibitory. Similar effect to that of BAP was found for NAA (0.5 mg l<SUP>-1</SUP>) and BAP + NAA (0.5 mg l<SUP>-1</SUP> + 0.5 mg l<SUP>-1</SUP>) in plantlet initiation. For <I>in vitro</I> growth of plantlets, 0.5 
mg l<SUP>-1</SUP> of BAP was the best for leaf and shoot growth compared to that of for BAP and NAA. However, for root growth of plantlets 1.0 mg l<SUP>-1</SUP> BAP + 1.0 mg l<SUP>-1</SUP> NAA was the most suitable. ]]></description>
<dc:creator>Israt Chowdhury, Abu Reza Md. Mahfuzur Rahman, M. Obaidul Islam and S. Matsui </dc:creator>
<dc:date>2003-09-01</dc:date>
<dc:title><![CDATA[Effects of Plant Growth Regulators on Callus Proliferation, Plantlet Regeneration and Growth of Plantlets of <I>Doritaenopsis</I> Orchid ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>221</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>214</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4562">
<title><![CDATA[<I>Spirulina </i> Species as a Source of Carotenoids and a-Tocopherol and its Anticarcinoma Factors</font> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=101&amp;articleno=4562</link>
<description><![CDATA[In the present study blue-green alga <I>Spirulina platensis </I>and<I> Spirulina maxima </I>were grown in batch culture at different nitrogen and NaCl concentrations, respectively. Both species were found to respond to nitrogen deficiency and high NaCl level by accumulation of large amounts of commercially important chemicals such as carotenoids and tocopherols. The higher carotenoids and a-tocopherol contents was obtained when <I>Spirulina</I> <I>sp</I> grown at low nitrogen level (51 ppm N), with values ranged from 19.82 to 24.1 mg g
<SUP>-1</SUP>
and from 533.2 to 978.5 
g Kg<SUP>-1</SUP> (dry weight, d.w.), respectively. Whilst, these values in cells grown in free nitrogen medium were ranged from 30.15 to 31.13 
mg g<SUP>-1</SUP>
and from 960.4 to 1325.7 
g Kg<SUP>-1</SUP> (d.w), respectively. The high performance liquid chromatography (HPLC) elution patter of total caroteniods extracted from <I>S. platensis </I> and <I> S maxima </I>
culture contained a-carotene (49.6 to 319.5 g g<SUP>-1</SUP>
lutein (0.06 to17.21 g 
g<SUP>-1</SUP>, astaxanthin (6.61 to 160.27 g g<SUP>-1</SUP>,
zeaxanthin (1.25 to 18.55 g g<SUP>-1</SUP>) and cryptoxanthin (1.41 to 20.13 g g<SUP>-1</SUP>). <I>S. maxima </I> accumulated a large amount of cryptoxanthin and zeaxanthin<I> </I>than that found in <I>S. platensis.</I> The effect of <I>Spirulina</I> species extracts containing various carotenoid compounds and tocopherols on the viability of Ehrlich ascites carcinoma cells (EACC) were evaluated. All algae extracts at different concentration of 200 and 400 ppm significant reduced the cell viability ranged from 89.11 to 5.25%. These extracts did not induce any significant changes in DNA fragmentation of treated EACC compared with untreated cells. But lactate dehydrogenase (LDH) and glutathione-S- transferase (GST) enzyme activities and glutathione level in treated EACC were significantly higher than that in untreated cells. These finding suggest that algae extracts may be reduce cell viability by other mechanism such as membrane lyases instead of apoptosis. Thus, <I>Spirulina </I>extract rich in carotenoids and tocopherols could be used as chemopreventive agents since they are relative non-toxic. ]]></description>
<dc:creator>Hanaa H. Abd El-Baky, Farouk K. El Baz and Gamal S. El-Baroty </dc:creator>
<dc:date>2003-09-01</dc:date>
<dc:title><![CDATA[<I>Spirulina </i> Species as a Source of Carotenoids and a-Tocopherol and its Anticarcinoma Factors</font> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>2</prism:volume>
<prism:endingPage>240</prism:endingPage>
<prism:publicationDate>2003</prism:publicationDate>
<prism:startingPage>222</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4563">
<title><![CDATA[Advancement in Genetic Modification Technologies Towards Disease Resistance and Food Crop Production]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4563</link>
<description><![CDATA[Genetically modified (GM) crops are cultivated presently in more than 40 million hectares in more than 13 countries in the World. The GM technology contained introduced microbial genes that provide tolerance to broad-spectrum herbicides such as glufosinate or glyophosate and resistance to pest and diseases. The continuous search for disease control strategies in crop production and the prospect of meeting the goals of global sustainable food crop production, has led to a significant interest in the GM technology as a modern tool for the introduction of disease resistance in crops. This review document attempts to discuss the progress of GM technology as a vital tool for the engineering of pathogen resistance in crops, the evolution of cloned disease resistance genes and the level of success of the GM disease resistant crops in commercial release. The GM technologies have the potential for producing improved high yielding disease resistant crops and better quality food products for consumption.]]></description>
<dc:creator>C.N. Fokunang, J.L. Beynon, K.A. Watson, N.H. Battey, J.M. Dunwell and E.A. Tembe-Fokunang</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Advancement in Genetic Modification Technologies Towards Disease Resistance and Food Crop Production]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>20</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>1</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4564">
<title><![CDATA[Kinetic and Stoichiometric Relationships of the Energy and Carbon Metabolism in the Culture of Microalgae]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4564</link>
<description><![CDATA[Some microalgae can grow metabolizing inorganic and organic carbon sources, which might occur simultaneously and independently, while energy is supplied by light and/or an organic carbon source. In this context, the contribution of each metabolism to total growth can be determined by quantitative analysis. The illumination of microalgal cells growing in the presence of organic substances, might cause an effect which can drive the carbon metabolism in different ways. When analyzing the growth of different strains of microalgae, some differences could be distinguished, between additive or inhibitory effect of light on heterotrophic metabolism in mixotrophic or photoheterotrophic growth. This manuscript proposes, the integration of a kinetic and stoichiometric metabolic model which explains the differences of carbon and energy utilization modes between mixotrophic and photoheterotrophic growth in microalgae. This model presumably discloses relevant independent facts between the mechanisms of photosynthesis and the oxidative metabolism of organic compounds, such as glucose and the importance of these differences on the production of biomass and secondary metabolites.]]></description>
<dc:creator>Katarzyna Chojnacka and Facundo-Joaquin Marquez-Rocha</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Kinetic and Stoichiometric Relationships of the Energy and Carbon Metabolism in the Culture of Microalgae]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>34</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>21</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4565">
<title><![CDATA[Isolation and Identification of Yeast Strains with High Beta-galactosidase Activity from Dairy Products]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4565</link>
<description><![CDATA[In this study of twenty-five samples which were collected from dairy producing 
  centers in the city of Isfahan, 30 yeast strains were isolated using Malt Extract 
  Broth (MEB) containing 0.1 gl<SUP>1</SUP> chloramphenicol 
  and Yeast Extract Glucose Chloramphenicol Agar (YGCA). Of the isolated strains, 
  11 with the ability to lactose fermentation were isolated (M1-M11). These strains 
  were identified by morphological and physiological properties. From these 11 
  strains, six were identified as <I>Kluyveromyces lactis</I>, four as <I>Kluyveromyces 
  marxianus</I> and one as <I>Candida versatilis</I>. In the next step, the amount 
  of produced single cell protein, SCP, from whey; whey including nitrogen supplementation 
  and whey with mixed yeast cultures in these strains was measured. Among these 
  strains, M2 that was identified as <I>K. lactis</I> had the most SCP production 
  from whey with 11.79 gl<SUP>1</SUP>. It was found 
  that the ammonium sulfate as a nitrogen source has a significant effect on biomass 
  yield so that amount of produced biomass of the M11 strain <I>(K. marxianus)</I> 
  increase from 11.54 gl<SUP>1</SUP> (from whey 
  without nitrogen supplementation) to 15.75 gl<SUP>1</SUP> 
  (in the presence of nitrogen source). The co-cultures of yeast strains with 
  <I>Saccharomyces cerevisiae</I> were evaluated. In the mixed yeast cultures 
  of these yeast strains and <I>S. cerevisiae</I>, the M2 strain which was identified 
  as <I>K. lactis</I> had the most biomass production, 22.38 gl<SUP>1</SUP>. 
  ONPG assay of beta-galactosidase in yeast strains found that a strain of <I>K. 
  lactis</I> (M2) has the highest enzyme activity (8103 Eu ml<SUP>1</SUP>). 
  These strains can be used for removal of whey pollutant, SCP &amp;amp; ethanol production 
  and treatment of lactose in dairy food.]]></description>
<dc:creator>I. Nahvi and H. Moeini</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Isolation and Identification of Yeast Strains with High Beta-galactosidase Activity from Dairy Products]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>40</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>35</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4566">
<title><![CDATA[Antimicrobial Activities of Cajanus cajan, Garcinia kola and Xylopia aethiopica on Pathogenic Microorganisms]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4566</link>
<description><![CDATA[The antimicrobial effect of the ethanol and aqueous extracts of locally available plants, <I>Cajanus cajan</I>, <I>Garcinia kola</I> and <I>Xylopia aethiopica</I> on <I>Staphylococcus aureus,</I> <I>Pseudomonas aeruginosa, Escherichia coli</I> and C<I>andida albicans</I> were evaluated. The agar gel diffusion and paper disk diffusion method were used to determine the inhibitory effects of both the leaves and seeds extract of the test plants on the test microorganisms. The plant extracts produced inhibition zones ranging from 3 to 22 mm against the test microorganisms. The ethanol extracts of the test plants were more effective in producing inhibition zones against the micro-organisms than water extracts. The extracts of <I>Cajanus cajan</I> produced wider zones of inhibition against <I>Candida albicans</I> than the other plants extracts.]]></description>
<dc:creator>G.O. Ezeifeka, M.U. Orji, T.I. Mbata and A.O. Patrick</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Antimicrobial Activities of Cajanus cajan, Garcinia kola and Xylopia aethiopica on Pathogenic Microorganisms]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>43</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>41</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4567">
<title><![CDATA[Rapid and Simultaneous Identification of Two <I>Salmonella enterica</I> Serotypes, Enteritidis and Typhimurium from Chicken and Meat Products by Multiplex PCR]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4567</link>
<description><![CDATA[In order to overcome the large volume of work required to detect and identify food samples that may contain <I> Salmonella  enterica</I>  serotypes  Enteritidis and Typhimurium, multiplex polymerase chain reaction (m-PCR) was used as a diagnostic tool to identify <I>Salmonella enterica</I>, <I>Salmonella enterica</I> ser. Enteritidis and Typhimurium in naturally contaminated meat and poultry products. Three sets of known <I>S. enterica</I> and serotypes <I>S. enteritidis</I> and <I>S. typhimurium</I> specific primers were applied to simultaneous identification of such pathogens in the most frequently used fresh and frozen meat (beef and lamb) and poultry (chicken) products (whole, cut, ground and processed) collected from eight locations within Irbid city (Jordan). Out of 93 samples, Only 21 (22.5%) samples contained serotype <I>S. typhimurium</I> alone. Nineteen samples (20%) showed the 312 bp  specific  band  for  serotype <I> S. enteritidis</I>   specific  band.  A  total of 28 (30%) samples showed only for <I>S. enterica</I> genus and 25 (26.8%) samples showed both serotypes <I>S. enteritidis </I>and <I>S. typhimurium</I>. In general, 46  (49.5%)  samples  contained  serotype <I> S.  typhimurium</I>, while  44  (47.3%)  samples  contained  serotype <I>S. enteritidis</I>. Multiplex PCR amplification was shown to be an effective and rapid method for the simultaneous identification of such pathogens in food samples.]]></description>
<dc:creator>Hanan Issa Malkawi and Raad Gharaibeh</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Rapid and Simultaneous Identification of Two <I>Salmonella enterica</I> Serotypes, Enteritidis and Typhimurium from Chicken and Meat Products by Multiplex PCR]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>48</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>44</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4568">
<title><![CDATA[A Single Ser<SUB>85</SUB>Ala Mutation Enhances the Catalytic Efficiency of 
  Subtilisin E from <I>Bacillus subtilis</I> 168]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4568</link>
<description><![CDATA[A single mutation of Ser for Ala was introduced into the highly conserved 83-Gly-Val-Ala-85 
region of AprE (subtilisin E) which resulted in the generation of a subtilisin 
mutant with an enhanced catalytic efficiency. The position of the mutation was 
placed in the conserved N-terminal end of the loop 
that connects a &amp;#946;-sheet with the &amp;#945;-helix containing the catalytic residue 
His<SUB>64</SUB>. The mutant Ser<SUB>85</SUB>Ala<I> apr</I>E gene was over 
expressed in a protease deficient <I>B. subtilis</I> genetic background and its 
product purified to homogeneity. The Ser<SUB>85</SUB>Ala AprE protein exhibited 
a catalytic efficiency two fold higher than that of its wild type parent AprE 
due to a larger <I>k<SUB>cat</SUB>.</I> Other biochemical properties such as thermal 
stability, optimum pH and temperature remained unchanged with respect to those 
exhibited by the pure wild type subtilisin. These results support the idea that 
mutations on the conserved stretch bend 83-Gly-Val-Ser-85 which connects two elements 
of secondary structure in AprE cause alterations on the catalytic properties of 
AprE and other subtilisins.]]></description>
<dc:creator>Eliel R. Romero-Garca, Joel A. Esquivel-Naranjo, Norma Ramrez-Ramrez, Jess Garca-Soto and Mario Pedraza-Reyes</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[A Single Ser<SUB>85</SUB>Ala Mutation Enhances the Catalytic Efficiency of 
  Subtilisin E from <I>Bacillus subtilis</I> 168]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>55</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>49</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4569">
<title><![CDATA[A Comparative Study of Axillary Shoot Proliferation from the Nodal Explants 
  of Three Varieties Pummelo (<I>Citrus grandis</I> [L.] Osb.)]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4569</link>
<description><![CDATA[Nodal segments of <I>in vitro</I> germinated seedlings of three pummelo varieties [Var.-1 (pulp is pink colour), Var.-2 (pulp is white colour) and Var.-3 (pulp is red colour)] were cultured on half-strength MS medium for axillary shoot proliferation. A large number of shoot buds were produced when such four weeks old culture were subcultured on half-strength MS medium containing 1.0 mg l<SUP>1</SUP> BAP. Roots were induced when the isolated individual shoots were cultured on half-strength MS medium containing 0.1 mg l<SUP>1</SUP> each of NAA, IBA or IAA. Cent percent root were observed on half-strength MS medium having 0.1 mg l<SUP>1</SUP> NAA. These <I>in vitro</I> grown plantlets were then successfully transferred to outside natural condition through successive phases of acclimatization. About 93% of the regenerated plantlets survived under <I>ex vitro</I> condition.]]></description>
<dc:creator>F. Begum, M.N. Amin, S. Islam and M.A.K. Azad</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[A Comparative Study of Axillary Shoot Proliferation from the Nodal Explants 
  of Three Varieties Pummelo (<I>Citrus grandis</I> [L.] Osb.)]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>62</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>56</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4570">
<title><![CDATA[Molecular Cloning of &amp;#946;-glucosidase Gene from <I>Trichoderma harzianum</I>]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4570</link>
<description><![CDATA[<I>Trichoderma harzianum </I>(E-58) was grown on Vogel`s 
medium containing glucose and xylan as carbon source. Glucose repressed the <I>&amp;#946;-</I>glucosidase 
production while xylan produced the enzyme in substantial amounts. Total RNA was 
isolated from mycelia of <I>Trichoderma harzianum</I> grown in medium containing 
xylan as carbon source. RT-PCR was performed on the isolated RNA. cDNA strand 
was synthesized by using oligo (dT)<SUB>18</SUB> primer. Specific primers were 
used to amplify <I>bgl</I> gene from cDNA. The <I>bgl</I> gene was ligated at 
SmaI site of pUC18 and transformed into <I>E. coli</I>.]]></description>
<dc:creator>Nighat Aslam, Farooq Latif, Sibtain Ahmed and Amer Jamil</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Molecular Cloning of &amp;#946;-glucosidase Gene from <I>Trichoderma harzianum</I>]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>66</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>63</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4571">
<title><![CDATA[Biosynthesis of Methanol from CO<sub>2</sub> and CH<sub>4</sub> by Methanotrophic Bacteria ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4571</link>
<description><![CDATA[Methanotrophs can oxidize methane to carbon dioxide through sequential reactions catalyzed by a series of enzymes including methane monooxygenase, methanol dehydrogenase, formaldehyde dehydrogenase and formate dehydrogenase. Reducing carbon dioxide to methanol is an opposite reaction of methanol oxidation, which requires a considerable amount of energy. So far there are no known organisms whose normal biological role is reduction of carbon dioxide to methanol. In this paper, we report that bioconversion of carbon dioxide to methanol was successfully achieved using resting cells of methanotrophic bacteria of <I>Methylosinus trichosporium</I> IMV 3011 as biocatalysts. Extracellular methanol accumulation has been found in the carbon dioxide incubations. The conversion of carbon dioxide to methanol is energy-intensive and requires reducing equivalent to push the reaction along against energy laws. For long-term maintenance of methanol synthesis, methane was selected as a substrate for regeneration of reducing equivalent. By alternate reaction and regeneration, the results show that resting cell of <I>M. trichosporium</I> IMV 3011 can be used for many times to catalyze the reduction of carbon dioxide, in which the origin of the reducing equivalent is methane. It is possible to theoretically deduce that the overall reaction for methanol synthesis can be completed by biocatalysis using greenhouse gases (carbon dioxide and methane) as raw materials without adding hydrogen. This new route should be environmentally benign and a selective process operating at room temperature and normal pressure. Also, it is theoretically possible that the overall reaction can produce methanol without adding to the greenhouse effect.]]></description>
<dc:creator>Jia-Ying Xin, Jun-Ru Cui, Jian-zhong Niu, Shao-feng Hua, Chun-Gu Xia, Shu-Ben Li and Li-Min Zhu</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Biosynthesis of Methanol from CO<sub>2</sub> and CH<sub>4</sub> by Methanotrophic Bacteria ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>71</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>67</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4572">
<title><![CDATA[The Effect of Silver Nitrate (Ethylene inhibitor) on <I>in vitro</I> Shoot 
  Development in Potato (<I>Solanum tuberosum</I> L.)]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4572</link>
<description><![CDATA[Ethylene produced by tissue, callus and plantlets in closed vessels may lead to abnormal plantlet growth and branching <I>in vitro</I>. Silver nitrate (AgNO<SUB>3</SUB>) is known as an ethylene inhibitor. Therefore, the objective of this study was to determine the effect of AgNO<SUB>3</SUB> on potato plantlets with measuring several characters. The results showed that MS basal medium supplemented with AgNO<SUB>3</SUB> resulted in an inhibitory effect on ethylene gas produced by potato plantlets. The response of the cultivars used showed genotypic dependence to different AgNO<SUB>3</SUB> concentrations. In general, the best results for all cultivars were obtained from 5 or 10 &amp;#956;M AgNO<SUB>3</SUB>. On the other hand, the higher AgNO<SUB>3</SUB> concentrations (25 and 50 &amp;#956;M) can be also used for cultivar Nicola and Desiree that initially had branching and abnormal plantlet growth.]]></description>
<dc:creator>Hakan Turhan</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[The Effect of Silver Nitrate (Ethylene inhibitor) on <I>in vitro</I> Shoot 
  Development in Potato (<I>Solanum tuberosum</I> L.)]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>74</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>72</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4573">
<title><![CDATA[Performance of Transgenic Bt Cotton Against Insect Pest Infestation ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4573</link>
<description><![CDATA[Studies were carried out to investigate insect infestation on transgenic Bt and non-Bt cotton varieties and genotypes.  The seeds of seven cotton varieties, viz., KMG-1, KMG-2, KMG-3, MS-1, MS-2 NIAB-78 and CRIS-134 were sown on May 15, 2002 in a completely randomized block design. The study comprised laboratory bioassay and field screening of different varieties and genotypes.  Laboratory study indicated that transgenic Bt cotton was highly toxic to <I>Earias vittella</I> causing 100% larval mortality.  While armyworm, <I>Spodoptera exigua</I> was tolerant, its mortality ranged between 13.3 to 53.3% on different varieties and genotypes.  The results of field study revealed that the highest mean population (1.66 insect per leaf) of jassid was recorded on KMG-3 followed by 1.95 and 1.52 insects leaf on KMG-2 and KMG-1, respectively.  Whitefly population ranged between 1.47 and 1.52 insects leaf on different varieties and genotypes. Whereas, thrips population remained fluctuating in different varieties and genotypes during the crop growth period. But genotypes like KMG-1, KMG-2 and KMG-3 which are crosses of Bt cotton and non-Bt cotton varieties were found harboring more thrips population. The larval population of spotted bollworm, <I>Earias</I> spp. indicated no infestation and live larvae were found on MS-1 and MS-2 varieties of Bt cotton. Maximum infestation of spotted bollworm was recorded on NIAB-78 (0.97 larva per plant) followed by other varieties and genotypes.]]></description>
<dc:creator>G.H. Abro, T.S. Syed, G.M. Tunio and M.A. Khuhro</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Performance of Transgenic Bt Cotton Against Insect Pest Infestation ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>81</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>75</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4574">
<title><![CDATA[Malathion Degradation by <I>Pseudomonas</I> Using Activated Sludge Treatment 
  System (Biosimulator)]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4574</link>
<description><![CDATA[This study was aimed at determining the growth kinetics and degradation potential of malathion by inoculation of the bacterial culture. Growth kinetics studies of <I>Pseudomonas</I> were determined by SPC technique using 4.0 mg L<SUP>1</SUP> dissolved oxygen (DO) in sterile undiluted nutrient broth and sterile diluted (1:10) nutrient broth, whereas the degradation studies were determined using high pressure liquid chromatographic (HPLC) techniques, which were conducted using continuous cultivation technique with similar DO level as that of growth kinetic studies using biosimulator, with two different set of conditions (with-culture; using pure culture of <I>Pseudomonas</I> and without-culture; indigenous microorganisms). A critical comparison of data revealed that at each sampling hour the viable population density was greater in the presence of undiluted nutrient broth than in the presence of diluted nutrient broth. Similarly the mean of degradation studies revealed that malathion degradation was more pronounced in studies with inoculation (with-culture) as compared with indigenous bacteria (without-culture). The study demonstrated that inoculation of bacterial culture studied under laboratory conditions can be used in bioremediation of environmental pollution caused by pesticides.]]></description>
<dc:creator>Hashmi Imran, Khan Mohammed Altaf and Jong B. Guk Kim</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Malathion Degradation by <I>Pseudomonas</I> Using Activated Sludge Treatment 
  System (Biosimulator)]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>89</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>82</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4575">
<title><![CDATA[First Report of Antifungal Properties of a New Strain of <I>Streptomyces plicatus 
</I>(Strain101)<I> </I>Against Four Iranian Phytopathogenic Isolates of <I>Verticillium 
dahliae</I>, A New Horizon in Biocontrol Agents]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4575</link>
<description><![CDATA[This is the first report on antifungal activity of a new strain of <I>Streptomyces plicatus </I>(strain101)<I> </I>against four Iranian phytopathogenic isolates of <I>Verticillium dahliae.</I> In the recent decades, biological control of plant diseases has received more attention mainly as a response to public concern about the use of hazardous chemicals in the environment. Soil Actinomycetes particularly <I>Streptomyces</I> spp.<I> </I>enhance soil fertility and have antagonistic activity against wide range of soil-borne plant pathogens. In search for metabolites of soil Actinomycetes having antifungal activity against four isolates of the cosmopolitan pathogen, <I>Verticillium dahliae</I> Klebahn, 110 isolates were screened. Among all, strain101 that was identified as a new strain of <I>S. plicatus</I>,  showed  high  level  of  activity  in  Agar  disk  and  Well-diffusion  methods. <I> S. plicatus</I> was propagated in submerged cultures and active crude was prepared upon which some biological characterizations performed. The active metabolite (s) is polar, soluble in H<SUB>2</SUB>O and methanol but insoluble in chloroform, dichloromethane or hexane. Antifungal activity composed of two types, mycelial inhibition, inhibition of microsclerotia and melanin production. Antifungal gene from <I>S.</I> <I>plicatus</I> Strain 101 may be a useful candidate for genetic engineering of agriculturally important crop plants for increased tolerance against <I>V. dahliae</I>.]]></description>
<dc:creator>Aghighi, S., G.H. Shahidi Bonjar and I. Saadoun </dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[First Report of Antifungal Properties of a New Strain of <I>Streptomyces plicatus 
</I>(Strain101)<I> </I>Against Four Iranian Phytopathogenic Isolates of <I>Verticillium 
dahliae</I>, A New Horizon in Biocontrol Agents]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>97</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>90</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4576">
<title><![CDATA[<I>In vitro</I> Coconut (<I>Cocos nucifera </I>L.) Embryo Culture in Bangladesh]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4576</link>
<description><![CDATA[Zygotic embryos of BARI Narikel 1, BARI Narikel 2, Srilankan Tall and Malaysian Dwarf were cultured on Y<SUB>3</SUB> basal nutrient medium. Germination percentages of embryos were recorded 93, 96, 89 and 40% in BARI Narikel 1, BARI Narikel 2, Srilankan Tall and Malaysian Dwarf respectively. Germination percentage was different due to the difference of physiological state of the embryos and/or difference in the genetic make up of the genotypes. Most of the embryos developed root and shoots simultaneously and survival rate was more then 60%. Significant difference in plant height, number of secondary roots, length of roots and transferable plantlet were found among the coconut genotypes.]]></description>
<dc:creator>M.M.H. Molla, M.S.A. Bhuiyan, M. Dilafroza Khanam and Pons Batugal</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[<I>In vitro</I> Coconut (<I>Cocos nucifera </I>L.) Embryo Culture in Bangladesh]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>101</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>98</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4577">
<title><![CDATA[Production of Lipids Rich in Omega 3 Fatty Acids from the Halotolerant Alga <I>Dunaliella salina</I> ]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=102&amp;articleno=4577</link>
<description><![CDATA[The effect of nitrogen limitation and salt stress on total lipid and unsaponifiable contents as well as fatty acid composition of <I>Dunaliella salina </I>were studied. The contents of total lipids, unsaponifiables and fatty acid composition were basically depend on NaCl and nitrogen concentration in the culture. The highest yield of total lipids (37.69%) and unsaponifiables (29.02%) was obtained in cells grown at 16% NaCl combined with 2.5 mM nitrogen. While, minimum yield occurred in cells grown in a culture containing 8% NaCl and 5 mM N. Cells grown at 16% NaCl combined with 2.5 mM N produced relatively higher proportion of polyunsaturated fatty acids (PUFAs), in particular C18:3<I>w</I>3 and C16:4<I>w</I>3. Increasing NaCl combined with decreasing N levels in the growth medium increased the total unsaturated fatty acids (TU) at the expense of total saturated fatty acids. At higher salinity, the total amounts of carotenoids and &amp;#945;-tocopherol in unsaponifiable fraction were significantly increased to reaching up to 12.03 and 4.10%. The results obtained suggest that <I>D. salina </I>cells containing high amount of total<I> </I>lipid, rich in<I> </I><I>w</I><SUB>3 </SUB>polyunsaturated fatty acids and antioxidant compounds in unsaponifiable lipid fraction may used as a supplemental ingredient or as a complete food to enhance the performance and state of the human body or improve a specific bodily function. ]]></description>
<dc:creator>Hanaa H. Abd El-Baky, Farouk K. El Baz and Gamal S. El-Baroty</dc:creator>
<dc:date>2004-01-01</dc:date>
<dc:title><![CDATA[Production of Lipids Rich in Omega 3 Fatty Acids from the Halotolerant Alga <I>Dunaliella salina</I> ]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>108</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>102</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4578">
<title><![CDATA[Neuropsychopharmacological Effects of Leaves and Seeds Extracts of <I>Datura fastuosa
</I>]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4578</link>
<description><![CDATA[Neuropsychopharmacological effects of aqueous extracts of leaves and seeds 
  of <I>Datura fastuosa</I> (<I>D. fastuosa</I>), a solanaceae recently introduced 
  in Congo as ornamental plant, were studied in rat and mice by oral administration 
  using classical methods. Results revealed that extracts of <I>D. fastuosa</I> 
  were well tolerated by rats. No mortality was observed until 3200 mg kg<sup>-</sup><SUP>1</SUP>. 
  The doses of 400 and 800 mg kg<sup>-</sup><SUP>1</SUP> of 
  leaves and seeds extracts increased motor activity, reduced slightly the duration 
  of barbituric sleeping, antagonized catalepsy and ptosis induced by haloperidol 
  and the immobility induced by forced swimming. <I>D. fastuosa </I>exhibited 
  analgesic effect in acetic acid test with tolerance phenomenon in the leaves 
  but not in the seeds extracts. Only the leaves extract reduced rectal temperature, 
  apomorphin hypothermia and increased water drinking.Those results showed that, 
  at the low doses, <I>D. fastuosa </I>has some antidepressant profile.]]></description>
<dc:creator>Ange Antoine Abena, Landry M.Miguel, Alain Mouanga, Jean M. Ouamba, Dorothe F. Sianard, Marie H. Thiebolt, Thophile C. Hondi-assah and Martin Diatewa</dc:creator>
<dc:date>2004-07-01</dc:date>
<dc:title><![CDATA[Neuropsychopharmacological Effects of Leaves and Seeds Extracts of <I>Datura fastuosa
</I>]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>113</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>109</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4598">
<title><![CDATA[Somatic Embryogenesis in <I>Phoenix dactylifera </I>L: Effect of Exogenous 
  Supply of Sucrose on Proteins, Sugars, Phenolics and Peroxidases Activities 
  During the Embryogenic Cell Suspension Culture]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4598</link>
<description><![CDATA[The present study was conducted  to determine the effect of three concentrations of usually used (1.5, 3 and 6%) of  sucrose  on the proliferation of date palm cell suspension culture. The medium containing 3% sucrose, leads to best results than 1.5 and 6% sucrose especially for JHL cultivar. In fact, when sucrose concentration increased from 1.5 to 3%, the embryogenic mass significantly  increased  from  2.15  to  14.6  g per flask and 8.7 to 10 g per flask, respectively for JHL and BSTN cultivars. The biochemical analysis showed that the maturation medium with 3% sucrose significantly increased the proteins (14.9 mg g<SUP>-1</SUP> FW for JHL cultivar and 5 mg g<SUP>-1</SUP> FW for BSTN cultivar) and sugars contents (22.5 and 22.7 mg g<SUP>-1</SUP> FW, respectively, for JHL and BSTN cultivars) in the embryogenic mass.  In  addition,  as  compared  to  1.5  and  6%,  the  use  of 3% sucrose enhanced phenolics contents (0.69 mg g<SUP>-1</SUP>FW) and peroxidases activities (2.9.10<SUP>3</SUP> n Kat g<SUP>-1</SUP>FW) in BSTN cultivar. ]]></description>
<dc:creator>J. Zouine and I. El Hadrami</dc:creator>
<dc:date>2004-07-01</dc:date>
<dc:title><![CDATA[Somatic Embryogenesis in <I>Phoenix dactylifera </I>L: Effect of Exogenous 
  Supply of Sucrose on Proteins, Sugars, Phenolics and Peroxidases Activities 
  During the Embryogenic Cell Suspension Culture]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>118</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>114</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4599">
<title><![CDATA[Chromosome and Gene Mapping Homology between River Buffalo, Cattle and Sheep using Molecular Markers]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4599</link>
<description><![CDATA[Chromosomal localization of sixteen bovine microsatellites in river buffalo 
  has been assigned in this study, using polymerase chain reaction and buffalo-hamster 
  somatic cell hybrids. These tested microsatellites were previously assigned 
  to sheep chromosomes. This study also aimed to confirm that the chromosome band 
  identity between river buffalo, cattle and sheep is a good indicator of genetic 
  homology between these closely related species. The correlation coefficients 
  between these tested microsatellites and other markers- representing syntenic 
  groups and chromosomes in river buffalo- was calculated to assign these microsatellites 
  to river buffalo chromosomes (BBU)). The results showed that BM719 is assigned 
  to BBU5q, BM827 to BBU12, BM1818 to BBU2p, BM1824 to BBU1q, BM2113 to BBU2q, 
  CSSM015 to BBU3p, CSSM034 to BBU4q, CSSM037 to BBU3q, CSSM043 to BBU1p, CSSM058 
  to BBU21, ILSTS011 to BBU15, ILSTS013 to BBU10, ILSTS019 to BBU5p, ILSTS029 
  to BBU6, ILSTS054 to BBU20 and ILSTS060 to BBU4p. The result also showed that 
  16 tested microsatellites are localized in river buffalo, cattle and sheep on 
  the equivalent chromosomes, which have chromosome- band homology, in these closely 
  related species belonging to Bovidae family, which has a high degree of chromosome 
  conservation between its members and where the bi-armed autosomes are formed 
  by centric fusions of acrocentric autosomes.]]></description>
<dc:creator>Othman E. Othman</dc:creator>
<dc:date>2004-07-01</dc:date>
<dc:title><![CDATA[Chromosome and Gene Mapping Homology between River Buffalo, Cattle and Sheep using Molecular Markers]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>125</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>119</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4600">
<title><![CDATA[Broadspectrim, A Novel Antibacterial from <I>Streptomyces</I> sp.]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4600</link>
<description><![CDATA[ Rapid emergence of antibacterial resistance is well documented as a serious 
  problem worldwide. This situation shows that the potencies of prevalent antibiotics 
  are decreasing steadily. This situation implies the need for searching new antimicrobials 
  to replace with invalidated ones or use in antibiotic rotation programs. In 
  a four years study, from 1,300 soil Actinomycete isolates collected from different 
  localities of Kerman, Hormozgan, Sistan and Baloochestan, south and south east 
  Provinces of Iran, <I>Streptomyces</I> sp. isolate No. 419 showed widest antibacterial 
  activity. The active principle named as Broadspectrim. It showed antibacterial 
  activity against wide range of G+ and G- bacteria as <I>Bacillus anthracis, 
  Bacillus subtilis, Citrobacter diversus</I>,<I> Citrobacter freundii</I>,<I> 
  Corynebacterium diphtheriae</I>,<I> Enterobacter</I> sp.,<I> Escherichia coli</I>,<I> 
  Klebsiella pneumoniae</I>,<I> Micrococcus luteum</I>,<I> Proteus vulgaris</I>,<I> 
  Proteus rettgeri</I>,<I> Proteus mirabilis</I>,<I> Proteus morganii</I>,<I> 
  Pseudomonas fluorescens, Pseudomonas aeruginosa, Pseudomonas syringae </I>pv<I> 
  syringae, Salmonella</I> Para Typhi A, B, C, D,<I> Salmonella typhi</I>,<I> 
  Sarcinia </I>sp.,<I> S. marcescens, Shigella dysentery</I>,<I> S. flexneri</I>, 
  <I>S. sonnei, Staphylococcus aureus</I>,<I> Staphylococcus epidermidis</I>,<I> 
  Streptococcus pneumoniae, Vibrio cholera </I>Eltor (INABA) and <I>Xanthomonas 
  </I>sp. but <I>Shigella flexneri</I> and <I>Staphylococcus albus</I> were resistant 
  to it.]]></description>
<dc:creator>G.H. Shahidi Bonjar, M.H. Fooladi, M.J. Mahdavi and A. Shahghasi </dc:creator>
<dc:date>2004-07-01</dc:date>
<dc:title><![CDATA[Broadspectrim, A Novel Antibacterial from <I>Streptomyces</I> sp.]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>130</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>126</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4601">
<title><![CDATA[<i>In vitro</I> Rapid Regeneration of Plantlets from Leaf Explant of Watermelon 
  (<I>Citrullus lanatus</I> Thumb.)]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4601</link>
<description><![CDATA[Plantlets regeneration were achieved in callus culture of leaf segments from 
  five days old field grown seedlings of <I>Citrulus lanatus</I> Thumb. Callus 
  induction and plant regeneration at various frequencies were observed using 
  different concentrations and combinations of growth regulators. The highest 
  percentage of callus induction was observed in MS medium supplemented with 2.5 
  mg L<SUP>-1</SUP> 2, 4-D. After transfer of this callus on MS medium supplemented 
  with 1.0 mg L<SUP>-1</SUP> BA+0.2 mg L<SUP>-1</SUP> NAA induce adventitious 
  shoots and developed into plant by further subculture in the same medium. NAA 
  (0.1 mg L<SUP>-1</SUP>) was found effective in the production of root. Plantlets 
  were acclimatized and subsequently transferred to the field. Survival of the 
  plantlets under <I>ex vitro</I> condition was 80%.]]></description>
<dc:creator>R.S. Sultana, M.A. Bari, M.H. Rahman, M.M. Rahman, N.A. Siddique and N. Khatun</dc:creator>
<dc:date>2004-07-01</dc:date>
<dc:title><![CDATA[<i>In vitro</I> Rapid Regeneration of Plantlets from Leaf Explant of Watermelon 
  (<I>Citrullus lanatus</I> Thumb.)]]></dc:title>
<dc:publisher>Asian Network for Scientific Information</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>3</prism:volume>
<prism:endingPage>135</prism:endingPage>
<prism:publicationDate>2004</prism:publicationDate>
<prism:startingPage>131</prism:startingPage>
</item>
<item rdf:about="http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4602">
<title><![CDATA[Development of Alfalfa Tolerant to Salinity Stress Using Organogenesis Technique]]></title>
<link>http://198.170.104.138/3/detail.php?id=1&amp;jid=biotech&amp;theme=3&amp;issueno=105&amp;articleno=4602</link>
<description><![CDATA[The possibility of using Organogenesis culture to evaluate salt tolerance of 
  cultivated alfalfa plants (<I>Medicago sativum </I>L<I>.</I>) was studied and 
  related to the response obtained by callus culture. The research was carried 
  out in the tissue Culture Lab, Department of Aridland Agriculture, College of 
  Food Systems, UAE University during seasons 2000/2001 including two Lab Experiments: 
  1) Callus Initiation and shoot formation and 2) Evaluation of <I>in vitro</I> 
  callus and plantlets under salinity stress. Seeds of alfalfa were sown in pots, 
  then leaves of the seedlings were separated to blades and petioles and placed 
  in jars containing 50 ml of the modified MS medium. For callus induction and 
  shoot formation, modified Murshig and Skoog and B5 were used in addition to 
  two growth regulators being 2,4-D and BA In order to evaluate the salt response 
  of the <I>in vitro</I> callus and plantlets, the induced calli and formed shoots 
  in Experiment I were taken and placed on modified Murshig and Skoog mineral 
  salts and B5. Sodium Chloride (NaCl) at four doses (0, 3000, 6000 and 9000 ppm) 
  were used in jars. The results of this study indicates that the best concentration 
  of 2.4-D and BA to obtain higher number and weight of callus and also higher 
  values of shoot weights can be obtained from the concentration of 2 mg L<SUP>-1</SUP> 
  in both cases. Increasing of NaCl salt concentration in the media causes significant 
  reduction in the seedling weight but positively correlated with Na and negatively 
  correlated with K concentration in the seedling tissues. NaCl salt concentration 
  of 6000 ppm was high enough to induce harmful effect on the seedling fresh weight, 
  whereas number of generated shoots formed roots was dramatically affected by 
  increasing NaCl concentration up to 3000 ppm and there was no shoots formed 
  roots establishe