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    <title>NISCAIR Online Periodicals Repository Collection: IJBT Vol.10(3) [July 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12102</link>
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    <item>
      <title>Detection of cardamom mosaic virus-related sequences in plant genomes</title>
      <link>http://nopr.niscair.res.in/handle/123456789/12118</link>
      <description>Title: Detection of cardamom mosaic virus-related sequences in plant genomes
&lt;br/&gt;
&lt;br/&gt;Authors: Jebasingh, T; Backiyarani, S; Manohari, C; Usha, R
&lt;br/&gt;
&lt;br/&gt;Abstract: Cardamom mosaic&#xD;
virus (CdMV)-related sequences have been found in cardamom plant genome.&#xD;
Integrated DNA was sequenced and was found identical to the 3′ end of NIb, the&#xD;
RNA dependent RNA polymerase gene of CdMV. This is the first report on the integration&#xD;
of potyviral partial NIb sequence into a plant genome. These&#xD;
CdMV-related&lt;sup&gt; &lt;/sup&gt;integrated DNA sequences were also detected in a few&#xD;
other plant genomes.
&lt;br/&gt;
&lt;br/&gt;Page(s): 369-371</description>
      <pubDate>Tue, 28 Jun 2011 22:58:59 GMT</pubDate>
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      <title>&lt;i&gt;In vitro&lt;/i&gt; multiplication of Merton I. 793–An apple rootstock suitable for replantation</title>
      <link>http://nopr.niscair.res.in/handle/123456789/12117</link>
      <description>Title: &lt;i&gt;In vitro&lt;/i&gt; multiplication of Merton I. 793–An apple rootstock suitable for replantation
&lt;br/&gt;
&lt;br/&gt;Authors: Soni, Mohit; Thakur, Manisha; Modgil, Manju
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;i&gt;In vitro&lt;/i&gt; shoot multiplication of Merton I. 793, a clonal apple rootstock,&#xD;
was achieved through terminal/axillary bud culture using Murashige and Skoog&#xD;
(MS) basal medium supplemented with 0.5-1.0 mg/L 6-benzyl amino purine (BA) and&#xD;
0.1 mg/L indole-3-butyric acid (IBA). Time of collection of explants, duration&#xD;
of surface sterilents and growth regulators added in the medium influenced the&#xD;
survival of explants and their bud break. Although, the shoots were multiplied&#xD;
on different concentrations of cytokinins and auxins, improved multiplication&#xD;
was achieved with 0.5 mg/L BA and 0.01 mg/L IBA. Of the three types of explants&#xD;
evaluated for shoot multiplication, shoot tips on elongation were found suitable&#xD;
for rooting whereas, nodal cuttings and cluster of small shoots for further&#xD;
multiplication. Low concentrations of α-naphthyl acetic acid (NAA) was proved&#xD;
to be more effective for rooting as compared to IBA and indole-3-acetic acid&#xD;
(IAA). To overcome profuse callus formation during rooting, activated charcoal&#xD;
was added. In another experiment, auxin was discontinued from the rooting&#xD;
medium after few days, thus, resulting in better rooting frequency (72%).&#xD;
Thirty plantlets of Merton I. 793 were successfully hardened after 7 wks, with&#xD;
around 80% survival rate.
&lt;br/&gt;
&lt;br/&gt;Page(s): 362-368</description>
      <pubDate>Tue, 28 Jun 2011 22:58:59 GMT</pubDate>
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      <title>Effect of organic solvents on solvent-tolerant &lt;i style=""&gt;Aeromonas &lt;strong&gt;hydrophila&lt;/strong&gt; &lt;/i&gt;IBB&lt;sub&gt;Po8&lt;/sub&gt; and &lt;i style=""&gt;Pseudomonas aeruginosa &lt;/i&gt;IBB&lt;sub&gt;Po10&lt;/sub&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/12116</link>
      <description>Title: Effect of organic solvents on solvent-tolerant &lt;i style=""&gt;Aeromonas &lt;strong&gt;hydrophila&lt;/strong&gt; &lt;/i&gt;IBB&lt;sub&gt;Po8&lt;/sub&gt; and &lt;i style=""&gt;Pseudomonas aeruginosa &lt;/i&gt;IBB&lt;sub&gt;Po10&lt;/sub&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Stancu, Mihaela Marilena
&lt;br/&gt;
&lt;br/&gt;Abstract: Alkanes (&lt;i style=""&gt;n&lt;/i&gt;-hexane, &lt;i style=""&gt;n&lt;/i&gt;-heptane) with logarithm of partition&#xD;
coefficient between &lt;i&gt;n&lt;/i&gt;-octanol and water (log &lt;i&gt;P&lt;sub&gt;OW&lt;/sub&gt;&lt;/i&gt;) 3.86&#xD;
to 4.39 were less toxic to &lt;i style=""&gt;Aeromonas &lt;/i&gt;&lt;strong&gt;&lt;i style=""&gt;hydrophila&lt;/i&gt;&lt;/strong&gt;&lt;i style=""&gt; &lt;/i&gt;IBB&lt;sub&gt;Po8&lt;/sub&gt; and &lt;i style=""&gt;Pseudomonas aeruginosa &lt;/i&gt;IBB&lt;sub&gt;Po10&lt;/sub&gt;&#xD;
as compared to aromatics (toluene, styrene, xylene isomers, ethylbenzene &amp;amp; propylbenzene)&#xD;
with log &lt;i style=""&gt;P&lt;sub&gt;OW&lt;/sub&gt;&lt;/i&gt;&lt;sub&gt; &lt;/sub&gt;2.64&#xD;
to 3.69. The toxicity of 0.5% (v/v) second phase of organic solvents to these&#xD;
bacteria could be predictable on the basis of the solvents’ log &lt;i&gt;P&lt;sub&gt;OW&lt;/sub&gt;&lt;/i&gt;.&#xD;
The tolerance,&#xD;
viability, adhesion and β-galactosidase&#xD;
activity of &lt;i style=""&gt;A. &lt;/i&gt;&lt;strong&gt;&lt;i style=""&gt;hydrophila&lt;/i&gt;&lt;/strong&gt;&lt;i style=""&gt; &lt;/i&gt;IBB&lt;sub&gt;Po8&lt;/sub&gt; and &lt;i style=""&gt;P. aeruginosa &lt;/i&gt;IBB&lt;sub&gt;Po10&lt;/sub&gt;&#xD;
cells in the presence of 0.5% (v/v) organic&#xD;
solvents varied significantly. The results indicated that &lt;i style=""&gt;A. &lt;/i&gt;&lt;strong&gt;&lt;i style=""&gt;hydrophila&lt;/i&gt;&lt;/strong&gt;&lt;i style=""&gt; &lt;/i&gt;IBB&lt;sub&gt;Po8&lt;/sub&gt; was more susceptible to&#xD;
organic solvents than &lt;i style=""&gt;P. aeruginosa &lt;/i&gt;IBB&lt;sub&gt;Po10&lt;/sub&gt;,&#xD;
whereas both the bacterial strains harbour plasmids. &lt;i style=""&gt;A. &lt;/i&gt;&lt;strong&gt;&lt;i style=""&gt;hydrophila&lt;/i&gt;&lt;/strong&gt;&lt;i style=""&gt; &lt;/i&gt;IBB&lt;sub&gt;Po8&lt;/sub&gt; did not posses hydrophobe/amphiphile efflux 1 (HAE1) transporter genes, while&lt;i style=""&gt; P. aeruginosa &lt;/i&gt;IBB&lt;sub&gt;Po10&lt;/sub&gt; did&#xD;
posses these genes. The adaptation mechanisms (modification of cell&#xD;
hydrophobicity, induction of β-galactosidase activity and changes in the&#xD;
membrane’s lipid and protein content) of&#xD;
bacterial cells, underlying solvent tolerance, in &lt;i style=""&gt;A. &lt;/i&gt;&lt;strong&gt;&lt;i style=""&gt;hydrophila&lt;/i&gt;&lt;/strong&gt;&lt;i style=""&gt; &lt;/i&gt;IBB&lt;sub&gt;Po8&lt;/sub&gt; and &#xD;
&lt;i style=""&gt;P. aeruginosa &lt;/i&gt;IBB&lt;sub&gt;Po10&lt;/sub&gt;&#xD;
showed a complex response to the&#xD;
presence of 0.5% (v/v) organic solvents in the culture medium. Bacterial strains able to survive in the presence&#xD;
of organic solvents could be used in two-phase biotransformation systems&#xD;
with whole cells for adequate bioremediation&#xD;
of heavily contaminated sites and could be&amp;nbsp; a source for new solvent-stable enzymes with&#xD;
different applications.
&lt;br/&gt;
&lt;br/&gt;Page(s): 352-361</description>
      <pubDate>Tue, 28 Jun 2011 22:58:59 GMT</pubDate>
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    <item>
      <title>Enhancement of dextransucrase activity of &lt;i style=""&gt;Pediococcus&lt;/i&gt; &lt;i style=""&gt;pentosaceus&lt;/i&gt; mutant SPAm1 by response surface methodology</title>
      <link>http://nopr.niscair.res.in/handle/123456789/12115</link>
      <description>Title: Enhancement of dextransucrase activity of &lt;i style=""&gt;Pediococcus&lt;/i&gt; &lt;i style=""&gt;pentosaceus&lt;/i&gt; mutant SPAm1 by response surface methodology
&lt;br/&gt;
&lt;br/&gt;Authors: Patel, Seema; Kothari, Damini; Goyal, Arun
&lt;br/&gt;
&lt;br/&gt;Abstract: In the present investigation, an optimal fermentation&#xD;
medium for the production of dextransucrase from mutant SPAm1 of a&#xD;
natural isolate of &lt;i style=""&gt;Pediococcus&lt;/i&gt; &lt;i style=""&gt;pentosaceus&lt;/i&gt;&#xD;
(GenBank&#xD;
Acc. No. EU569832) was developed following response surface&#xD;
method. A two-level Plackett-Burman design (PBD) and five-level Central&#xD;
composite design (CCD) was combined to optimize the medium composition for&#xD;
enhancement of the dextransucrase activity of SPAm1.&#xD;
A second-order model equation was suggested and validated experimentally. The&#xD;
model adequacy was very satisfactory as the coefficient of determination was 0.958. The optimum values for the tested&#xD;
variables were; sucrose 55.2 g/L; beef&#xD;
extract 2.3 g/L and Tween 80 8.3 mL/L. The predicted dextransucrase activity after response optimization was 15.9 U/mL,&#xD;
whereas the experimental value was 15.6&#xD;
U/mL at 16 h of incubation, which showed a 3.2-fold enhancement over the&#xD;
enzyme activity (4.9 U/mL) of&#xD;
mutant SPAm1 given by the unoptimized medium. However, the&#xD;
increase in dextransucrase activity by SPAm1 after optimization of the medium&#xD;
was an outstanding 4.6-fold&#xD;
higher&#xD;
over that of the wild-type &lt;i style=""&gt;P.&lt;/i&gt; &lt;i style=""&gt;pentosaceus &lt;/i&gt;from the unoptimized medium&#xD;
(3.4 U/mL).
&lt;br/&gt;
&lt;br/&gt;Page(s): 346-351</description>
      <pubDate>Tue, 28 Jun 2011 22:58:59 GMT</pubDate>
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