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    <title>NISCAIR Online Periodicals Repository Collection: IJBT Vol.05(3) [July 2006]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5431</link>
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      <title>Biopulping studies using an effluent isolate &lt;i&gt;Cuwularia lunata &lt;/i&gt;LW6</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7764</link>
      <description>Title: Biopulping studies using an effluent isolate &lt;i&gt;Cuwularia lunata &lt;/i&gt;LW6
&lt;br/&gt;
&lt;br/&gt;Authors: Narkhede, K P; Vidhale, N N
&lt;br/&gt;
&lt;br/&gt;Abstract: The lignin is unwanted constituent&#xD;
for a pulp and paper manufacturer, which must be removed for getting good&#xD;
quality paper. The aim of bio-delignification of raw material is to make&#xD;
pulping process easier, to save energy requirements, to improve pulp properties&#xD;
and to minimize pollution. The present study aims to find suitability of&#xD;
isolate &lt;i&gt;Curvularia lunata&lt;/i&gt; LW6 for biopulping of sugarcane bagasse. The&#xD;
organism was screened from effluent of pulp and paper mill and rested for lignolytic&#xD;
ability. The isolate produced the enzyme lignin peroxidase (3.31 U/mg of&#xD;
protein) and laccase (6.12 UImL). It showed good saprophytic ability (38.14&#xD;
cm2) on sterile bagasse when supplemented with glucose and yeast extract as cosubstrate. The solid-state fermentation of&#xD;
bagasse for biopulping resulted in loss of weight by 21.66%, while lignin content and kappa number decreased by 44.05%&#xD;
and 40.78%, respectively. The chemical pulping showed 55.25% reduction in kappa&#xD;
number; however, it required high temperature, pressure and alkaline medium.&#xD;
The mutagenesis studies showed slight&#xD;
&#xD;
decrease in cellulase activity of&#xD;
the isolate.&#xD;
&#xD;
 
&lt;br/&gt;
&lt;br/&gt;Page(s): 385-388</description>
      <pubDate>Wed, 28 Jun 2006 22:58:59 GMT</pubDate>
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    <item>
      <title>Efficient &lt;i style=""&gt;Pseudomonas putida&lt;/i&gt; for degradation of &lt;i style=""&gt;p&lt;/i&gt;-nitrophenol</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7763</link>
      <description>Title: Efficient &lt;i style=""&gt;Pseudomonas putida&lt;/i&gt; for degradation of &lt;i style=""&gt;p&lt;/i&gt;-nitrophenol
&lt;br/&gt;
&lt;br/&gt;Authors: Kulkarni, Meenal; Chaudhari, Ambalal
&lt;br/&gt;
&lt;br/&gt;Abstract: Exploration of &lt;i style=""&gt;Pseudomonas putida&lt;/i&gt; for controlling&#xD;
environmental (&lt;i style=""&gt;p&lt;/i&gt;-nitrophenol) PNP&#xD;
pollution revealed that 0.5 OD inoculum at 600 nm degraded 100 ppm of PNP&#xD;
completely under the ambient conditions within 24 h as established by&#xD;
UV-visible spectrophotometric and TLC analysis of treated broth and confirmed&#xD;
the same by HPLC analysis. An attempt to elucidate the mechanism of PNP&#xD;
degradation indicated that (i) it was oxidative with a stoichiometric release&#xD;
of nitrite, (ii) PNP was converted to hydroquinone, which accumulated in the&#xD;
presence of 2,2'-dipyridyl, (iii) hydroquinone was the&#xD;
first product of ring oxygenation and nitrite removal, as confirmed by TLC and&#xD;
HPLC analysis and (iv) concomitant formation of a keto acid by ring fission,&#xD;
which was confirmed by Rothera's test.
&lt;br/&gt;
&lt;br/&gt;Page(s): 411-415</description>
      <pubDate>Wed, 28 Jun 2006 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Integrated biological approach for the enhanced degradation of lindane</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7762</link>
      <description>Title: Integrated biological approach for the enhanced degradation of lindane
&lt;br/&gt;
&lt;br/&gt;Authors: Nagpal, Varima; Paknikar, K M
&lt;br/&gt;
&lt;br/&gt;Abstract: Lindane is a&#xD;
persistent organic pollutant (POP) and its removal from various environmental&#xD;
compartments is a global priority. In the present study, three lindane&#xD;
degrading bacterial cultures, viz. &lt;i style=""&gt;Pseudoarthrobacter&#xD;
&lt;/i&gt;sp., &lt;i style=""&gt;Pseudomonas &lt;/i&gt;sp. and &lt;i style=""&gt;Klebsiella &lt;/i&gt;sp., were selected from among&#xD;
ten isolates obtained from lindane-exposed soils by enrichment culture&#xD;
technique. The cultures exhibited a maximum lindane degradation efficiency of&#xD;
~50%, having little significance in bioremediation. However, in the presence of&#xD;
protozoa (ciliates) obtained from the same enrichment culture, lindane&#xD;
degradation efficiency of bacterial cultures increased to the tune of 90-92%&#xD;
with concomitant formation of 1,2,4-trichlorobenzene, a key degradation&#xD;
product. Lindane degradation by the bacterial cultures was also found to get&#xD;
enhanced by 10-15% in the presence of root exudates of lindane-tolerant plants,&#xD;
viz. corn, chili and coriander, even though these plants were unable to uptake&#xD;
any lindane and thus were unsuitable for phytoremediation &lt;i style=""&gt;per se&lt;/i&gt;. These data highlight the need for an intensive investigation&#xD;
on (a) bacteria-protozoa interactions for bioremediation of POPs and (b) use of&#xD;
POP-degrading bioinoculants in the rhizospheric soil of resistant plants as a&#xD;
possible alternative, in the absence of a viable conventional remedial option.
&lt;br/&gt;
&lt;br/&gt;Page(s): 400-406</description>
      <pubDate>Wed, 28 Jun 2006 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Micropropagation of &lt;i style=""&gt;Azadirachta indica &lt;/i&gt;A. Juss. via cotyledonary nodes</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7761</link>
      <description>Title: Micropropagation of &lt;i style=""&gt;Azadirachta indica &lt;/i&gt;A. Juss. via cotyledonary nodes
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, A Rajasekhar; Bavaji, M; Rao, J V S
&lt;br/&gt;
&lt;br/&gt;Abstract: An efficient protocol for micropropagation of &lt;i style=""&gt;Azadirachta indica &lt;/i&gt;A. Juss., a&#xD;
medicinally important plant, has been standardized. Cotyledonary nodes (1 cm&#xD;
long) excised from 15-20 d old &lt;i style=""&gt;in vitro-&lt;/i&gt;germinated&#xD;
seedlings were used as explants. The seeds were germinated on half strength MS&#xD;
medium devoid of phytohormones. Cotyledonary nodes were cultured on MS medium&#xD;
supplemented with different concentrations of cytokinins (BA/TDZ/2-ip) and&#xD;
auxins (2,4-D and NAA). Maximum shoot proliferation from single explant was obtained&#xD;
on MS media incorporated with TDZ (1.5 &lt;img src='/image/spc_char/micro.gif' border=0&gt; &lt;i style=""&gt;M&lt;/i&gt;), 2,4-D (0.5 &lt;img src='/image/spc_char/micro.gif' border=0&gt; &lt;i style=""&gt;M&lt;/i&gt;), adenine sulphate&#xD;
(40 mg/L), glutamine (100 mg/L) and thiamine HC1 (10 mg/L). &lt;i style=""&gt;In vitro-&lt;/i&gt;produced shoots were induced&#xD;
roots on half strength MS medium supplemented with a range of IBA concentrations&#xD;
(0.5-5.0 &lt;img src='/image/spc_char/micro.gif' border=0&gt; &lt;i style=""&gt;M&lt;/i&gt;).&#xD;
However, the highest frequency of root proliferation was observed on half&#xD;
strength MS medium supplemented with 2.0 &lt;img src='/image/spc_char/micro.gif' border=0&gt; &lt;i style=""&gt;M&lt;/i&gt; IBA. The regenerants&#xD;
were transferred to field conditions after acclimatization with a success rate&#xD;
of 80%
&lt;br/&gt;
&lt;br/&gt;Page(s): 309-311</description>
      <pubDate>Wed, 28 Jun 2006 22:58:59 GMT</pubDate>
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