<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/3477" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/3477</id>
  <updated>2026-10-10T10:10:44Z</updated>
  <dc:date>2026-10-10T10:10:44Z</dc:date>
  <entry>
    <title>&lt;span style="mso-bidi-language:HI"&gt;Rhizobial lipopolysaccharide as the receptor in lectin&lt;i&gt;-Rhizobium &lt;/i&gt;interaction &lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/30393" />
    <author>
      <name>Bhattacharya, Indranil</name>
    </author>
    <author>
      <name>Biswas, Sagarika</name>
    </author>
    <author>
      <name>Das, Rakha H</name>
    </author>
    <author>
      <name>Das, Hasi R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/30393</id>
    <updated>2016-07-20T06:45:04Z</updated>
    <published>2004-04-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="mso-bidi-language:HI"&gt;Rhizobial lipopolysaccharide as the receptor in lectin&lt;i&gt;-Rhizobium &lt;/i&gt;interaction &lt;/span&gt;
Authors: Bhattacharya, Indranil; Biswas, Sagarika; Das, Rakha H; Das, Hasi R
Abstract: &lt;span style="mso-bidi-language:HI"&gt;Rhizobial specificity was examined on the basis of&#xD;
interaction between legume lectins (peanut, pea and soybean) and different&#xD;
rhizobial species (various bradyrhizobia specific for peanut, P 14-93 and SB16).&#xD;
Legume lectins showed higher affinity towards host-specific &lt;i&gt;Rhizobium &lt;/i&gt;and&#xD;
lipopolysaccharides (LPS) isolated from those particular rhizobia. Two LPS mutants&#xD;
of peanut-specific &lt;i&gt;Bradyrhizobium &lt;/i&gt;sp. (&lt;i&gt;Arachis&lt;/i&gt;)&lt;i&gt; &lt;/i&gt;strain GN17&#xD;
were isolated by Tn5 mutagenesis. These mutants (GN17MI and GNI7M2) were&#xD;
characterized by their higher hydrophobicity with respect to the parent cells.&#xD;
The hexose content in exopolysaccharides. (EPS) and LPS of the mutants was&#xD;
found reduced significantly, whereas 2-keto-3-deoxyoctulosonic acid (Kdo) and&#xD;
uronic acid in LPS were less by 20-times and thrice, respectively in the&#xD;
mutants. Glucose was the major sugar in LPS from all the strains. However,&#xD;
glucosamine appeared only in the mutants. Spectrofluorimetric analysis showed&#xD;
that LPS from GN17Ml mutant interacted most significantly with peanut root&#xD;
agglutinin or lectin (PRA II). The results indicate that LPS on the surface of&#xD;
rhizobial cells is the possible receptor for lectin.&#xD;
&#xD;
&lt;/span&gt;
Page(s): 89-95</summary>
    <dc:date>2004-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>An insight into molecular mechanism of endocytosis</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/30392" />
    <author>
      <name>Neekhra, Nidhi</name>
    </author>
    <author>
      <name>Padh, Harish</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/30392</id>
    <updated>2016-07-20T06:45:04Z</updated>
    <published>2004-04-01T00:00:00Z</published>
    <summary type="text">Title: An insight into molecular mechanism of endocytosis
Authors: Neekhra, Nidhi; Padh, Harish
Abstract: &lt;span style="mso-bidi-language:HI"&gt;Endocytosis involving pinocytosis, phagocytosis&#xD;
and receptor-mediated pathway is a central process involved in numerous&#xD;
cellular events: receptor recycling, nutrient uptake, transcytosis, antigen&#xD;
processing and presentation, pathogen uptake etc. Traditionally, the process&#xD;
has been studied using uptake kinetics and immunocytochemistry. In last few&#xD;
decades, additional tools, like mutant analysis, density shift, semi-intact and&#xD;
cell-free systems and electromagnetic separation have&#xD;
&#xD;
&lt;span style="mso-bidi-language:HI"&gt;helped us to obtain molecular insight into many of&#xD;
the' steps involved in endocytosis. New chemical entities, like clathrin and coatomer&#xD;
proteins involved in internalization have been fully characterized.&#xD;
Biomolecules involved in vesicle budding diffusion reactions, like ARF (ADP&#xD;
ribosylation factors), COPs (coal proteins), and SNAREs (soluble&#xD;
N-ethylmaleimide sensitive factor attachment protein receptors) have been&#xD;
identified and characterized. Compartment specific molecules, like Rab have&#xD;
also added to our understanding of complex process of endocytosis. Collectively&#xD;
these have led us to an era of molecular endocytosis. The present review gives&#xD;
an overview of the process and describes some of the molecular events of the&#xD;
endocytic process. It also describes methods and approaches used in deciphering&#xD;
the events at cellular and molecular levels.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;
Page(s): 69-80</summary>
    <dc:date>2004-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Measurement of urinary oxalate by grain sorghum leaf oxalate oxidase immobilized to affixed alkylamine glass beads</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/3646" />
    <author>
      <name>Kumari, M</name>
    </author>
    <author>
      <name>Pundir, C S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/3646</id>
    <updated>2009-04-02T16:30:33Z</updated>
    <published>2004-04-01T00:00:00Z</published>
    <summary type="text">Title: Measurement of urinary oxalate by grain sorghum leaf oxalate oxidase immobilized to affixed alkylamine glass beads
Authors: Kumari, M; Pundir, C S
Abstract: Oxalate in urine was measured by grain Sorghum leaf oxalate oxidase conjugated to alkyl amine glass beads affixed in a beaker. The minimum detection limit was 0.05 mM/L in urine. Recovery of added oxalate in urine was 80.5% and within and between assay, coefficients of variation (CV) were &lt;4% and &lt;5.5%, respectively. Urinary oxalate values obtained by the present method showed a good correlation (r = 0.947) with those by Sigma kit method. The method is not only free from tedious handling of free glass beads and Cl⁻ interference, but also has longer stability and reusability of immobilized enzyme compared to that of barley root and forage Sorghum leaf.
Page(s): 102-106</summary>
    <dc:date>2004-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Absorption spectral study of 3, 4-dihydroxy phenyl alanine (DOPA) with Nd (III) in aqueous medium</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/3645" />
    <author>
      <name>Bhatt, Prashant N</name>
    </author>
    <author>
      <name>Pathak, Trupti V</name>
    </author>
    <author>
      <name>Mehta, Jignasu P</name>
    </author>
    <author>
      <name>Misra, Sudhindra N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/3645</id>
    <updated>2009-03-31T16:30:54Z</updated>
    <published>2004-04-01T00:00:00Z</published>
    <summary type="text">Title: Absorption spectral study of 3, 4-dihydroxy phenyl alanine (DOPA) with Nd (III) in aqueous medium
Authors: Bhatt, Prashant N; Pathak, Trupti V; Mehta, Jignasu P; Misra, Sudhindra N
Abstract: Spectroscopic properties of Nd (III)-DOPA in aquated organic solvents are investigated through absorption difference and comparative absorption spectroscopy involving 4f-4f transitions. The change in coordination in different conditions is observed from the absorption intensity analysis when Nd (III) interacts with DOPA. The interaction induced substantial changes in the intensities of 4f-4f bands and their perturbation was reflected through oscillator strength Judd-Ofelt intensity (T) parameters. It is suggested that the changes in the oscillator strengths of different 4f-4f bands and Judd-Ofelt intensity (T) parameters can be used to predict in vivo intracellular complexation of DOPA with Ca(II) through Nd (III)-DOPA absorption spectral studies in-vitro as both Nd (III) and Ca(II) have unique similarity in their coordination behaviour.
Page(s): 123-127</summary>
    <dc:date>2004-04-01T00:00:00Z</dc:date>
  </entry>
</feed>

