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    <title>NISCAIR Online Periodicals Repository Collection: IJEB Vol.46(11) [November 2008]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/4406</link>
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      <title>Assembly of recombinant coat protein of sugarcane streak mosaic virus into potyvirus-like particles&lt;i style=""&gt;&lt;/i&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4651</link>
      <description>Title: Assembly of recombinant coat protein of sugarcane streak mosaic virus into potyvirus-like particles&lt;i style=""&gt;&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Hema, M; Reddy, Ch V Subba; Savithri, H S; Sreenivasulu, P
&lt;br/&gt;
&lt;br/&gt;Abstract: Coat protein (CP) gene of sugarcane streak mosaic virus-AP isolate (SCSMV-AP) was expressed in &lt;i&gt;E. coli&lt;/i&gt; and recombinant CP (SCSMV-AP rCP) was purified by linear sucrose density gradient centrifugation. Observation of purified SCSMV-AP rCP under electron microscope revealed the presence of potyvirus-like particles (PVLPs). The assembled particles were shown to encapsidate CP gene transcripts by slot-blot hybridization.
&lt;br/&gt;
&lt;br/&gt;Page(s): 793-796</description>
      <pubDate>Wed, 29 Oct 2008 22:58:59 GMT</pubDate>
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      <title>Efficacy of 4-methyl-7-hydroxy coumarin derivatives against vectors &lt;i style=""&gt;Aedes aegypti &lt;/i&gt;and &lt;i&gt;Culex quinquefasciatus&lt;/i&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4650</link>
      <description>Title: Efficacy of 4-methyl-7-hydroxy coumarin derivatives against vectors &lt;i style=""&gt;Aedes aegypti &lt;/i&gt;and &lt;i&gt;Culex quinquefasciatus&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Deshmukh, Madhavi; Pawar, Pushpa; Joseph, Mary; Phalgune, Usha; Kashalkar, Rajashree; Deshpande, Nirmala  R
&lt;br/&gt;
&lt;br/&gt;Abstract: 4-Methyl-7-hydroxy coumarin is considered as a lead molecule as a biopesticide. Its mono bromo and tribromo derivatives were synthesized. Two more derivatives were synthesized by acylation. Compound 1 (3,6,8-tribromo-7-hydroxy-4-methyl-chromen-2-one) was found to be the most potent against IV&lt;sup&gt;th&lt;/sup&gt; instar larvae of &lt;i style=""&gt;C. quinquefasciatus&lt;/i&gt; and  &lt;i style=""&gt;A. aegypti&lt;/i&gt; &lt;i&gt; &lt;/i&gt;the&lt;i&gt; &lt;/i&gt;LC&lt;sub&gt;50&lt;/sub&gt; being 1.49  and 2.23 ppm respectively. It showed 100% larval mortality at 25 ppm against &lt;i style=""&gt;A. aegypti&lt;/i&gt; and at 10 ppm against C&lt;i style=""&gt;. quinquefasciatus&lt;/i&gt;. Compounds 1 and 2 (3,6,8-tribromo-7-hydroxy-4-methyl-chromen-2’-oxo-2H-chromen-7-yl acetate) showed remarkable ovicidal activity. Significant reduction of 80-85% hatching of eggs of both mosquito species was observed at the highest dose of 100 ppm. The hatched larvae showed 100% mortality in the successive instars. Compounds 3 and 4 (3-bromo-7-hydroxy-4-methyl-chromen-2-one and 3-bromo-4-methyl-2’-oxo-2H-chromen-7-yl acetate) showed moderate activity against both mosquito species.
&lt;br/&gt;
&lt;br/&gt;Page(s): 788-792</description>
      <pubDate>Wed, 29 Oct 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Screening of natural phenolic compounds for potential to inhibit bacterial cell division protein FtsZ</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4649</link>
      <description>Title: Screening of natural phenolic compounds for potential to inhibit bacterial cell division protein FtsZ
&lt;br/&gt;
&lt;br/&gt;Authors: Rastogi, Neerja; Domadia, Prerna; Shetty, Sangeeta; Dasgupta, Debjani
&lt;br/&gt;
&lt;br/&gt;Abstract: FtsZ plays an important role in bacterial cell division by polymerizing to form the Z ring at the site of cytokinesis. Phytochemicals are known to disrupt bacterial cell division through inhibition of FtsZ assembly. In the present study phytochemicals like eugenol, &lt;i style=""&gt;trans-&lt;/i&gt;cinnamic acid, 4-formyl cinnamic acid, naringenin and caffeic acid were were tested for their potential to inhibit cell division. Effect of these antimicrobial compounds on the growth of &lt;i style=""&gt;E. coli&lt;/i&gt; was determined and the inhibition of FtsZ assembly &lt;i style=""&gt;in vitro&lt;/i&gt; was investigated. The present study revealed &lt;i style=""&gt;trans&lt;/i&gt;-cinnamic acid as the most potent inhibitor of FtsZ assembly.
&lt;br/&gt;
&lt;br/&gt;Page(s): 783-787</description>
      <pubDate>Wed, 29 Oct 2008 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Wound healing activity of &lt;i&gt;Sesamum indicum &lt;/i&gt;L seed and oil in rats</title>
      <link>http://nopr.niscair.res.in/handle/123456789/4648</link>
      <description>Title: Wound healing activity of &lt;i&gt;Sesamum indicum &lt;/i&gt;L seed and oil in rats
&lt;br/&gt;
&lt;br/&gt;Authors: Kiran, Kotade; Asad, Mohammed
&lt;br/&gt;
&lt;br/&gt;Abstract: The seeds of &lt;i&gt;S. indicum&lt;/i&gt; L (Pedaliaceae) are used traditionally in the folklore for the treatment of various kinds of wounds. The present study was undertaken to verify the effect of &lt;i&gt;S. indicum&lt;/i&gt; seeds and its oil&lt;i&gt; &lt;/i&gt;on experimentally induced excision wound, incision wound, burn wound and dead space wound models in rats. &lt;i&gt;Aloe vera &lt;/i&gt;was used as standard wound healing agent. A formulation of seeds and oil was prepared in carbopol at 2.5% and 5% concentrations and applied to the wounds. In the excision and burn wound models, the so treated animals showed significant reduction in period of epithelization and wound contraction (50%). In the incision wound model a significant increase in the breaking strength was observed. Seeds and oil&lt;i&gt; &lt;/i&gt;treatment (250 mg and 500 mg/kg; po) in dead space wound model, produced a significant increase in the breaking strength, dry weight and hydroxyproline content of the granulation tissue. The results suggest that &lt;i&gt;S. indicum &lt;/i&gt;seeds and oil&lt;i&gt; &lt;/i&gt;applied topically or administered orally possesses wound healing activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 777-782</description>
      <pubDate>Wed, 29 Oct 2008 22:58:59 GMT</pubDate>
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