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    <title>NISCAIR Online Periodicals Repository Community: IJBT Vol.08 [2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/2929</link>
    <description />
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      <title>Retroviral vectors and gene therapy: An update</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6157</link>
      <description>Title: Retroviral vectors and gene therapy: An update
&lt;br/&gt;
&lt;br/&gt;Authors: Maurya, S K; Srivastava, Sushant; Joshi, R K
&lt;br/&gt;
&lt;br/&gt;Abstract: Gene therapy aims at treatment of diseases by transfer of genetic material&#xD;
into specific cells of a patient. So the transduction of appropriate target&#xD;
cell is critical. Retroviruses infect nearly every cell in the target&#xD;
population and become integrated in host cell genome for a stable expression.&#xD;
All retroviruses have only three structural genes &lt;i&gt;gag, pol &lt;/i&gt;and&lt;i&gt; env&lt;/i&gt;,&#xD;
except for lentiviruses where two other genes &lt;i&gt;tat, rev &lt;/i&gt;and four&#xD;
accessory genes are required (&lt;i&gt;vif, vpu, nif, vpr&lt;/i&gt;). There are two&#xD;
components of retroviral vector system—i) Packaging cell lines, which provide&#xD;
the products of &lt;i&gt;gag, pol &lt;/i&gt;&amp; &lt;i&gt;env &lt;/i&gt;genes but are unable to&#xD;
package itself as they lack the &lt;img src='/image/spc_char/shi.gif'&gt; sequence, and ii) retroviral&#xD;
vectors where &lt;i&gt;gag, pol &lt;/i&gt;and &lt;i&gt;env&lt;/i&gt; are deleted but &lt;img src='/image/spc_char/shi.gif'&gt; sequence along with LTR is present. Several other types of vectors are&#xD;
also described.
&lt;br/&gt;
&lt;br/&gt;Page(s): 349-357</description>
      <pubDate>Mon, 28 Sep 2009 22:58:59 GMT</pubDate>
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    <item>
      <title>Isolation of morphovariants through plant regeneration in &lt;i&gt;Agrobacterium rhizogenes&lt;/i&gt; induced hairy root cultures of &lt;i&gt;Plumbago rosea&lt;/i&gt; L.</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6156</link>
      <description>Title: Isolation of morphovariants through plant regeneration in &lt;i&gt;Agrobacterium rhizogenes&lt;/i&gt; induced hairy root cultures of &lt;i&gt;Plumbago rosea&lt;/i&gt; L.
&lt;br/&gt;
&lt;br/&gt;Authors: Satheeshkumar, K; Jose, Binoy; Soniya, E V; Seeni, S
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt;&#xD;
&#xD;
&lt;i style=""&gt;In vitro &lt;/i&gt;raised shoots of &lt;i&gt;Plumbago rosea&lt;/i&gt; L. were infected with A4 strain of &lt;i&gt;Agrobacterium&#xD;
rhizogenes&lt;/i&gt; to initiate hairy root formation, which produced 3.0±0.33 hairy&#xD;
roots per incision on explants in 20 d incubation. Southern blot analysis&#xD;
confirmed the integration of T-DNA into the genome of the roots. The hairy&#xD;
roots were cultured on MS agar medium supplemented with 2.0 mg/L BAP to induce&#xD;
the formation of shoots (3.2±0.24) of 0.2-0.4 cm length in 7-8 wks.&#xD;
Isolated shoots were multiplied through sub culturing in the presence of 0.5&#xD;
mg/L BAP and the resultant shoots were subjected to combined elongation (3.29±0.16 cm) and rooting&#xD;
(12.6±0.57) in a medium supplemented with 0.1 mg/L IBA. The rooted plants were&#xD;
invariably abnormal with short internodes and wrinkled leaves showing 34.5%&#xD;
establishment in 2 months after transplantation in polybags and rearing under&#xD;
75% sunlight in a shade house. Out of 38 plants transferred to the field, 20&#xD;
(52.6%) survived and grew over 10-month period to reveal variations in&#xD;
morphological and growth characters. The growth of all the hairy root-derived&#xD;
plants was slow to varied extent, 13 among them retaining actively growing&#xD;
hairy roots and shoots having short internodes and expanded leaves, one with&#xD;
emerging normal shoot and a tuberous root in the midst of the abnormal shoot&#xD;
and hairy roots and the rest with hairy roots as well as 1-2 normal roots and&#xD;
abnormal shoots having wrinkled leaves. The biomass production ability of the&#xD;
transformed plants contributed by foliage and root characters was poor compared&#xD;
to plants raised from the nodal explants of normal shoot cultures. Southern&#xD;
blot analysis of DNA further confirmed the presence of bacterial T-DNA in these&#xD;
established plants in the field after 10 months. The demonstrated hairy root&#xD;
regeneration system including field establishment of the plants may be useful&#xD;
for scoring new variations especially in non-seed setting &lt;i style=""&gt;P. rosea&lt;/i&gt;.&lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 435-441</description>
      <pubDate>Mon, 28 Sep 2009 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Studies on microbial transformation of albendazole by soil fungi</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6155</link>
      <description>Title: Studies on microbial transformation of albendazole by soil fungi
&lt;br/&gt;
&lt;br/&gt;Authors: Prasad, G Shyam; Girisham, S; Reddy, S M
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="country-region"&gt;&lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="place"&gt;&#xD;
&#xD;
Soil&#xD;
enrichment technique was followed to isolate the fungi capable of performing&#xD;
biotransformation of albendazole. Among the 5 fungi isolated, &lt;i style=""&gt;Aspergillus fumigatus&lt;/i&gt;, &lt;i style=""&gt;A. niger&lt;/i&gt; and &lt;i style=""&gt;Penicillium chrysogenum&lt;/i&gt; could transform albendazole to one&#xD;
metabolite and &lt;i style=""&gt;Fusarium moniliforme&lt;/i&gt;&#xD;
could transform albendazole to two metabolites. The transformation was&#xD;
confirmed by HPLC. Based on LC-MS-MS analysis, the metabolites formed were&#xD;
predicted to be albendazole sulfoxide and albendazole sulfone. The results&#xD;
support that the soil enrichment is a promising technique for isolation of&#xD;
fungi with industrial applicability, viz. production of active metabolites from&#xD;
drugs.&lt;/smarttagtype&gt;&lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 425-429</description>
      <pubDate>Mon, 28 Sep 2009 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Cost-effective fermentative production of calcium lactate using BISS (below Indian standard sugar) and &lt;i&gt;Spirulina&lt;/i&gt; hydrolysate</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6154</link>
      <description>Title: Cost-effective fermentative production of calcium lactate using BISS (below Indian standard sugar) and &lt;i&gt;Spirulina&lt;/i&gt; hydrolysate
&lt;br/&gt;
&lt;br/&gt;Authors: Yadav, A K; Chaudhari, A B; Kothari, R M
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt;&#xD;
&#xD;
&#xD;
&#xD;
Batch fermentation of BISS (below Indian&#xD;
standard sugar) in combination with &lt;i style=""&gt;Spirulina&lt;/i&gt;&#xD;
hydrolysate (SH) has been successfully explored at 50 L scale to replace costly&#xD;
glucose and yeast extract (YE) medium as a source of complex nutrients to&#xD;
produce calcium lactate economically by using &lt;i style=""&gt;Lactobacillus delbruckii&lt;/i&gt;. This has led to optimization of a&#xD;
protocol for cost-effective production of calcium lactate. Reduction in&#xD;
duration of fermentation has potential to provide additional benefits of (i)&#xD;
more batches per unit capital investment and time, (ii) less consumption of&#xD;
utilities, and (iii) higher output per unit labour cost.&#xD;
&#xD;
&lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 418-424</description>
      <pubDate>Mon, 28 Sep 2009 22:58:59 GMT</pubDate>
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