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    <title>NISCAIR Online Periodicals Repository Collection: IJEB Vol.50(11) [November 2012]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14886</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14944" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14943" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14942" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/14941" />
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    <title>The Collection's search engine</title>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14944">
    <title>&lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Cloning and expression of a small heat and salt tolerant protein (&lt;i&gt;Hsp&lt;/i&gt;22) from &lt;i&gt;Chaetomium globosum&lt;/i&gt;&lt;/span&gt;</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14944</link>
    <description>Title: &lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Cloning and expression of a small heat and salt tolerant protein (&lt;i&gt;Hsp&lt;/i&gt;22) from &lt;i&gt;Chaetomium globosum&lt;/i&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Aggarwal, Rashmi; Gupta, Sangeeta; Sharma, Sapna; Banerjee, Sagar; Singh, Priyanka
&lt;br/&gt;
&lt;br/&gt;Abstract:   The present&#xD;
study reports molecular characterization of small heat shock protein gene in&#xD;
Indian isolates of &#xD;
&lt;i style="mso-bidi-font-style:normal"&gt;Chaetomium globosum&lt;/i&gt;, &lt;i style="mso-bidi-font-style:normal"&gt;C. perlucidum, C. reflexum, C. cochlioides &lt;/i&gt;and&lt;i style="mso-bidi-font-style:normal"&gt; C. cupreum. &lt;/i&gt;Six isolates of &lt;i style="mso-bidi-font-style:normal"&gt;C. globosum&lt;/i&gt; and other species showed a&#xD;
band of 630bp using specific primers. Amplified cDNA product of &lt;i style="mso-bidi-font-style:normal"&gt;C. globosum&lt;/i&gt; (Cg 1) cloned and sequenced&#xD;
showed 603bp open reading frame encoding 200 amino-acids. The protein sequence had a molecular mass of 22 kDa&#xD;
and was therefore, named Hsp22. BlastX analysis revealed that the gene codes for a protein homologous to previously&#xD;
characterized &lt;i style="mso-bidi-font-style:normal"&gt;Hsp&lt;/i&gt;22.4 gene&#xD;
from &lt;i&gt;C. globosum&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt; (&lt;span style="mso-fareast-font-family:Calibri;letter-spacing:-.1pt" lang="EN-GB"&gt;AAR36902.1,&#xD;
XP 001229241.1) &lt;span style="letter-spacing:-.1pt;mso-bidi-font-style:&#xD;
italic" lang="EN-GB"&gt;and shared 95%&#xD;
identity in amino acid sequence. It also showed varying degree of similarities&#xD;
with small Hsp protein from &lt;i&gt;Neurospora&lt;/i&gt; spp. (60%), &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;Myceliophthora&lt;/i&gt; sp. (59%), &lt;i style="mso-bidi-font-style:normal"&gt;Glomerella&lt;/i&gt;&#xD;
sp. (50%), &lt;i style="mso-bidi-font-style:normal"&gt;Hypocrea&lt;/i&gt; sp. (52%), and &lt;i style="mso-bidi-font-style:normal"&gt;Fusarium&lt;/i&gt; spp. (51%). This gene was&#xD;
further cloned into pET28a (+) and transformed&#xD;
&lt;i&gt;E. coli&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt; BL21 cells were&#xD;
induced by IPTG, and the expressed protein of 30 kDa was analyzed by SDS-PAGE. &#xD;
&lt;span style="mso-bidi-font-style:italic"&gt;The IPTG induced transformants&#xD;
displayed significantly greater resistance to NaCl and Na&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;&#xD;
stresses. &#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 826-832</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14943">
    <title>Enhanced rosmarinic acid production in cultured plants of two species of &lt;i style="mso-bidi-font-style:normal"&gt;Mentha&lt;/i&gt;</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14943</link>
    <description>Title: Enhanced rosmarinic acid production in cultured plants of two species of &lt;i style="mso-bidi-font-style:normal"&gt;Mentha&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Roy, Debleena; Mukhopadhyay, Sandip
&lt;br/&gt;
&lt;br/&gt;Abstract:   In the present investigation an attempt has&#xD;
been made to enhance rosmarinic acid level in plants, grown&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt; in vitro&lt;/i&gt;, of &#xD;
2 species of &lt;i style="mso-bidi-font-style:normal"&gt;Mentha&lt;/i&gt; in presence of 2&#xD;
precursors in the nutrient media during culture. For &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;in vitro&lt;/i&gt; culture establishment and shoot bud multiplication, MS&#xD;
basal media were used supplemented with different concentrations and&#xD;
combinations of different growth regulator like NAA (α-napthaleneacetic acid),&#xD;
BAP (6-benzylaminopurine). The medium containing NAA (0.25 mg/L) and BAP (2.5&#xD;
mg/L) gave the highest potentiality of shoot formation (average 58.0 numbers of&#xD;
shoots) per explant for &lt;i style="mso-bidi-font-style:normal"&gt;Mentha piperita&lt;/i&gt;&#xD;
L. and the medium containing BAP (2.0 mg/L) gave the highest potentiality of&#xD;
shoot (average 19.2 numbers of shoots) formation per explant for &lt;i style="mso-bidi-font-style:normal"&gt;Mentha arvensis &lt;/i&gt;L. The complete plants&#xD;
were regenerated in above mentioned media after 8 weeks of subculture. For &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;/i&gt; enhancement of rosmarinic acid&#xD;
production, the 2 precursors tyrosine (Tyr) and phenylalanine (Phe) were added&#xD;
in the nutrient media at different levels (0.5 mg/L to 15.0 mg/L). Tyrosine was&#xD;
found to be very effective for augmenting rosmarinic acid content in &lt;i style="mso-bidi-font-style:normal"&gt;Mentha piperita&lt;/i&gt; L. It nearly increased the production up to 1.77 times. In case of &lt;i style="mso-bidi-font-style:normal"&gt;Mentha arvensis&lt;/i&gt; L., phenylalanine significantly affected the production of rosmarinic&#xD;
acid and the production was nearly 2.03 times more than the control. No&#xD;
significant increase in biomass was observed after addition of these precursors&#xD;
indicating that the added amino acids acting as precursors for rosmarinic acid&#xD;
synthesis were readily utilized in producing rosmarinic acid without promoting&#xD;
growth. Total protein profile also revealed the presence of a specific band in&#xD;
polyacrylamide gel electrophoresis.
&lt;br/&gt;
&lt;br/&gt;Page(s): 817-825</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14942">
    <title>An efficient &lt;i style="mso-bidi-font-style: normal"&gt;in vitro &lt;/i&gt;regeneration protocol for a natural dye yielding plant, &lt;i style="mso-bidi-font-style:normal"&gt;Strobilanthes flaccidifolious&lt;/i&gt; Nees., from nodal explants</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14942</link>
    <description>Title: An efficient &lt;i style="mso-bidi-font-style: normal"&gt;in vitro &lt;/i&gt;regeneration protocol for a natural dye yielding plant, &lt;i style="mso-bidi-font-style:normal"&gt;Strobilanthes flaccidifolious&lt;/i&gt; Nees., from nodal explants
&lt;br/&gt;
&lt;br/&gt;Authors: Deb, Chitta Ranjan; Arenmongla, T
&lt;br/&gt;
&lt;br/&gt;Abstract: &amp;amp;nbsp; Adventitious&#xD;
shoot buds formation from axillary buds of nodal segments of &lt;i style="mso-bidi-font-style:normal"&gt;S. flaccidifolious&lt;/i&gt; was achieved on MS&#xD;
medium containing sucrose (3%, w/v), and α-naphthalene acetic acid (NAA; 3 µM)&#xD;
and benzyl adenine (3 µM) in combination. The nodal segments were primed on&#xD;
‘Growtak Sieve’ for 48 h on MS medium containing sucrose (2%), polyvinyl pyrollidone&#xD;
(200 mgL&lt;sup&gt;-1&lt;/sup&gt;) as antioxidant. About 80% of primed nodal segments&#xD;
responded positively and formed ~12 adventitious shoot buds per explants from&#xD;
explants collected during October-November months of every year. The shoot buds&#xD;
converted into plantlets on MS medium containing sucrose (3%) and kinetin (3&#xD;
µM) where ~7 micro shoots developed per subculture after 8 weeks of culture.&#xD;
The regenerated micro shoots induced average 14 roots/ plant on medium&#xD;
containing NAA (3 µM). The regenerates were hardened for 6-7 weeks on medium&#xD;
with ½MS salt solution and sucrose (2%) under normal laboratory condition&#xD;
before transferring to potting mix. About 70% transplants survived after two&#xD;
months of transfer.
&lt;br/&gt;
&lt;br/&gt;Page(s): 810-816</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/14941">
    <title>Virgin coconut oil improves hepatic lipid metabolism in rats–compared with  copra oil, olive oil and sunflower oil</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14941</link>
    <description>Title: Virgin coconut oil improves hepatic lipid metabolism in rats–compared with  copra oil, olive oil and sunflower oil
&lt;br/&gt;
&lt;br/&gt;Authors: Arunima, S; Rajamohan, T
&lt;br/&gt;
&lt;br/&gt;Abstract: Effect of virgin coconut oil (VCO) on lipid&#xD;
levels and regulation of lipid metabolism compared with copra oil (CO), olive&#xD;
oil (OO), and sunflower oil (SFO) has been reported. Male Sprague-Dawley rats&#xD;
were fed different oils at 8% level &#xD;
for 45 days along with synthetic diet. Results showed that VCO feeding&#xD;
significantly lowered (&lt;i&gt;P&lt;/i&gt;&lt;0.05) levels of &#xD;
total cholesterol, LDL+ VLDL cholesterol, Apo B and triglycerides in serum and&#xD;
tissues compared to rats fed CO, OO and SFO, while HDL-cholesterol and Apo A1&#xD;
were significantly (&lt;i&gt;P&lt;/i&gt;&lt;0.05) higher in serum of rats fed VCO than&#xD;
other &#xD;
groups. Hepatic lipogenesis was also down regulated in VCO fed rats, which was&#xD;
evident from the decreased activities of enzymes viz., HMG CoA reductase,&#xD;
glucose-6-phosphate dehydrogenase, isocitrate dehydrogenase and malic enzyme. &#xD;
In addition, VCO significantly (&lt;i&gt;P&lt;/i&gt;&lt;0.05) increased the activities of&#xD;
lipoprotein lipase, lecithin cholesterol acyl transferase and enhanced&#xD;
formation of bile acids. Results demonstrated hypolipidemic effect of VCO by&#xD;
regulating the synthesis &#xD;
and degradation of lipids.
&lt;br/&gt;
&lt;br/&gt;Page(s): 802-809</description>
  </item>
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