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    <title>NISCAIR Online Periodicals Repository Community: IJBT Vol.10 [2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10943</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12988" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12987" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12986" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12985" />
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12988">
    <title>Biodegradation of poultry feathers by a novel bacterial isolate &lt;i style=""&gt;Bacillus altitudinis&lt;/i&gt; GVC11</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12988</link>
    <description>Title: Biodegradation of poultry feathers by a novel bacterial isolate &lt;i style=""&gt;Bacillus altitudinis&lt;/i&gt; GVC11
&lt;br/&gt;
&lt;br/&gt;Authors: Kumar, E Vijay; Srijana, M; Chaitanya, K; Reddy, Y Harish Kumar; Reddy, Gopal
&lt;br/&gt;
&lt;br/&gt;Abstract: Keratinolytic microorganisms have great&#xD;
importance in feather waste degradation and its use for improvement of&#xD;
livestock feed and production of protein hydrolysates. &lt;i&gt;Bacillus altitudinis &lt;/i&gt;GVC11,&#xD;
a novel, raw chicken feather degrading bacterium, previously isolated and identified&#xD;
by morphological, biochemical and 16s rDNA sequencing in our laboratory, was&#xD;
used in the present study. It was&#xD;
grown in a medium containing only poultry feathers as sole carbon and nitrogen&#xD;
source. GVC11 was able to degrade white and dark chicken feathers in 48 and 96&#xD;
h, respectively. Degradation of white feather including rachis and barbules was&#xD;
observed under electron microscope. The optimum conditions for keratinase&#xD;
production and feather degradation by GVC11 were &lt;i style=""&gt;p&lt;/i&gt;H 9, 37&lt;sup&gt;o&lt;/sup&gt;C and 200 rpm. Essential&#xD;
amino acids like phenyl alanine, valine, leucine, isoleucine and threonine were&#xD;
observed in supernatant obtained after feather degradation at concentrations of&#xD;
124, 88, 19, 17, and 11 &lt;img src='/image/spc_char/micro.gif' border=0&gt;mols, respectively per 100 mL of broth. Biodegradation&#xD;
of feathers by &lt;i&gt;B. altitudinis &lt;/i&gt;GVC11 can be used for keratinase and&#xD;
oligopeptide production and degraded feather biomass can also be utilized as&#xD;
animal feed supplement.
&lt;br/&gt;
&lt;br/&gt;Page(s): 502-507</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12987">
    <title>Pyrene biodegradation by free and immobilized&lt;i style=""&gt; &lt;/i&gt;cells of&lt;i style=""&gt; Mycobacterium frederiksbergense&lt;/i&gt; using a solvent encapsulated system</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12987</link>
    <description>Title: Pyrene biodegradation by free and immobilized&lt;i style=""&gt; &lt;/i&gt;cells of&lt;i style=""&gt; Mycobacterium frederiksbergense&lt;/i&gt; using a solvent encapsulated system
&lt;br/&gt;
&lt;br/&gt;Authors: Sarma, Saurabh Jyoti; Pakshirajan, Kannan; Saamrat, K B G
&lt;br/&gt;
&lt;br/&gt;Abstract: Polycyclic&#xD;
aromatic hydrocarbons (PAHs) are classified as hazardous pollutants in the&#xD;
environment due to their toxic, mutagenic and recalcitrant nature. Compared to&#xD;
other methods, biodegradation using microorganisms seems to be attractive&#xD;
alternative for treating PAH contaminated environment. However, there are&#xD;
limitations because of its low aqueous solubility and negligible&#xD;
bioavailability to the degrading microbes. The present study investigated&#xD;
biodegradation of pyrene, a model PAH compound, using both free and calcium&#xD;
alginate immobilized cells of &lt;i style=""&gt;Mycobacterium&#xD;
frederiksbergense. &lt;/i&gt;To overcome the bioavailability problem,&lt;i style=""&gt; &lt;/i&gt;organic phase (silicone oil) containing&#xD;
the PAH compound was encapsulated using chitosan coated sodium alginate-polyvinyl&#xD;
alcohol beads for subsequent use in the biodegradation experiments. Prior to&#xD;
the biodegradation experiments, characterization of the silicone oil&#xD;
encapsulated beads and the cell immobilized beads were also performed. In&#xD;
pyrene biodegradation experiments using the free cells, following an initial&#xD;
lag phase of 4 d, ~90% degradation was achieved at 400 and 800 mg/L initial&#xD;
pyrene concentrations. On the other hand, immobilized cells in beads of ~700 &#xD;
&lt;img src='/image/spc_char/micro.gif' border=0&gt;m size showed better&#xD;
performance even at a very high initial concentration of 2000 mg/L.
&lt;br/&gt;
&lt;br/&gt;Page(s): 496-501</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12986">
    <title>RAPD profile and rDNA sequence analysis of &lt;i style=""&gt;Talaromyces flavus&lt;/i&gt; and &lt;i style=""&gt;Trichoderma&lt;/i&gt; species</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12986</link>
    <description>Title: RAPD profile and rDNA sequence analysis of &lt;i style=""&gt;Talaromyces flavus&lt;/i&gt; and &lt;i style=""&gt;Trichoderma&lt;/i&gt; species
&lt;br/&gt;
&lt;br/&gt;Authors: Chakraborty, B N; Chakraborty, U; Sunar, K; Dey, P L
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;i style=""&gt;Talaromyces flavus&lt;/i&gt; isolated from paddy rhizosphere exhibited&#xD;
phosphate solubilizing activity &lt;i style=""&gt;in vitro&lt;/i&gt;&#xD;
and positively influenced the growth of &lt;i style=""&gt;Oryza&#xD;
sativa&lt;/i&gt;, &lt;i style=""&gt;Cicer arietinum&lt;/i&gt; and &lt;i style=""&gt;Vigna radiata&lt;/i&gt; under green house&#xD;
conditions. Besides, isolates of &lt;i style=""&gt;Trichoderma&#xD;
harzianum&lt;/i&gt; and &lt;i style=""&gt;T. asperellum&lt;/i&gt;&#xD;
obtained from agricultural field of Darjeeling&#xD;
hills showed antifungal activities against fungal pathogens. Phylogenetic analysis of all&#xD;
these isolates were carried out by sequencing the internal transcribed spacer&#xD;
regions (ITS1 &amp; ITS4) of the ribosomal DNA of &lt;i style=""&gt;T. flavus&lt;/i&gt; and &lt;i style=""&gt;T. harzianum&lt;/i&gt;&#xD;
using universal primers. The sequences were aligned against ex-type strain&#xD;
sequences from NCBI GenBank. Genetic relatedness among the isolates was studied&#xD;
using random decamer primers. UPGMA cluster analysis showed that the similarity&#xD;
coefficient ranged from 0.37 to 1 for &lt;i style=""&gt;T.&#xD;
flavus&lt;/i&gt; and 0.68 to 1 for &lt;i style=""&gt;T. harzianum&lt;/i&gt;.&#xD;
The open reading frame (ORF) analysis of 18S rDNA sequence of &#xD;
&lt;i style=""&gt;T. harzianum &lt;/i&gt;revealed that the&#xD;
sequence contains in total of four ORFs, encoding 159 amino acids with an&#xD;
estimated molecular mass of 17.84 kDa. The sequences of ITS1 region have been&#xD;
used as the reference sequence, which may be used for future study involving&#xD;
the identification and taxonomy of both &lt;i style=""&gt;T.&#xD;
flavus&lt;/i&gt; and &lt;i style=""&gt;Trichoderma&lt;/i&gt; isolates.
&lt;br/&gt;
&lt;br/&gt;Page(s): 487-495</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12985">
    <title>Cloning and expression of an intronless gene encoding endoglucanase from &lt;i style=""&gt;Aspergillus fumigatus&lt;/i&gt; MKU1</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12985</link>
    <description>Title: Cloning and expression of an intronless gene encoding endoglucanase from &lt;i style=""&gt;Aspergillus fumigatus&lt;/i&gt; MKU1
&lt;br/&gt;
&lt;br/&gt;Authors: Meera, B; Vanitha, M C; Ramani, G; Manjula, A; Gunasekaran, P
&lt;br/&gt;
&lt;br/&gt;Abstract: Endoglucanase&#xD;
(carboxymethyl cellulase) production by an alkali tolerant fungus &lt;i style=""&gt;Aspergillus fumigatus&lt;/i&gt; MKU1 was&#xD;
characterized under submerged fermentation conditions. The carboxymethyl cellulase&#xD;
(CMCase) activity was optimal at &lt;i style=""&gt;p&lt;/i&gt;H&#xD;
5.0 and 60°C. Intronless gene &lt;i style=""&gt;eng&lt;/i&gt;61&#xD;
coding for endoglucanase from &lt;i style=""&gt;A.&#xD;
fumigatus &lt;/i&gt;MKU1 was cloned and sequenced. The &lt;i style=""&gt;eng&lt;/i&gt;61 gene contains 993 bp ORF encoding a polypeptide of 330 amino&#xD;
acids. &lt;i style=""&gt;In silico&lt;/i&gt; analysis of the&#xD;
translated sequence revealed the presence of C-terminal cellulose binding&#xD;
module and signal peptide cleavage site between 20&lt;sup&gt;th&lt;/sup&gt; and 21&lt;sup&gt;st&lt;/sup&gt;&#xD;
amino acids. The &lt;i style=""&gt;eng&lt;/i&gt;61 was cloned&#xD;
in pET30b and expressed in &lt;i style=""&gt;Escherichia&#xD;
coli &lt;/i&gt;BL21 DE3. Thus, an intronless endoglucanase gene from an alkali&#xD;
tolerant strain of &lt;i style=""&gt;A. fumigatus &lt;/i&gt;has&#xD;
been cloned and expressed.
&lt;br/&gt;
&lt;br/&gt;Page(s): 480-486</description>
  </item>
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