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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19768" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/19768</id>
  <updated>2026-10-16T17:19:59Z</updated>
  <dc:date>2026-10-16T17:19:59Z</dc:date>
  <entry>
    <title>Production of Plumbagin (5-hydroxy-2-methyl-1, 4-naphthoquinone) in Callus and Cell Suspension Cultures of &lt;i&gt;Plumbago indica&lt;/i&gt; Linn.</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19881" />
    <author>
      <name>Satheeshkumar, K</name>
    </author>
    <author>
      <name>Seeni, S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19881</id>
    <updated>2013-07-19T16:34:02Z</updated>
    <published>2002-07-01T00:00:00Z</published>
    <summary type="text">Title: Production of Plumbagin (5-hydroxy-2-methyl-1, 4-naphthoquinone) in Callus and Cell Suspension Cultures of &lt;i&gt;Plumbago indica&lt;/i&gt; Linn.
Authors: Satheeshkumar, K; Seeni, S
Abstract: The relationship between growth and&#xD;
plumbagin (5-hydroxy-2-methyl-l, 4-naphthoquinone) formation in callus and cell&#xD;
suspension cultures of &lt;i&gt;Plumbago indica &lt;/i&gt;was investigated. Semi-friable callus&#xD;
was induced on young stem and leaf segments in MS solid medium containing&#xD;
1.5-2.5 mgl&lt;sup&gt;-1&lt;/sup&gt; 2, 4-D plus 0.5-1.5 mgl&lt;sup&gt;-1 &lt;/sup&gt;KN. Cell suspension&#xD;
cultures were established from stem-derived semi-friable calli and cells released&#xD;
from aseptic leaf segments. Quantitative analysis of plumbagin in callus and&#xD;
cell cultures at different periods of growth revealed an increase in&#xD;
concentration of plumbagin with the increase in growth of cultures. Plumbagin&#xD;
level in both culture systems on unit dry wt basis was same throughout the&#xD;
growth of callus (0.05 mg/g, dry wt) and cell cultures (0.028 mg/g, dry wt).
Page(s): 305-308</summary>
    <dc:date>2002-07-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;i&gt;&lt;span style="font-size:12.0pt;line-height:115%; font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:HI"&gt;In Vitro &lt;/span&gt;&lt;/i&gt;&lt;span style="font-size:12.0pt;line-height:115%;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:HI"&gt;Regeneration and Hydroxycitric Acid Production in Tissue Cultures of &lt;i&gt;Garcinia indica &lt;/i&gt;Chois&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19880" />
    <author>
      <name>Kulkarni, Manik D</name>
    </author>
    <author>
      <name>Deodhar, Manjushri A</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19880</id>
    <updated>2013-07-25T16:33:23Z</updated>
    <published>2002-07-01T00:00:00Z</published>
    <summary type="text">Title: &lt;i&gt;&lt;span style="font-size:12.0pt;line-height:115%; font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:HI"&gt;In Vitro &lt;/span&gt;&lt;/i&gt;&lt;span style="font-size:12.0pt;line-height:115%;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:HI"&gt;Regeneration and Hydroxycitric Acid Production in Tissue Cultures of &lt;i&gt;Garcinia indica &lt;/i&gt;Chois&lt;/span&gt;
Authors: Kulkarni, Manik D; Deodhar, Manjushri A
Abstract: &lt;i&gt;Garcinia indica &lt;/i&gt;is a rich source of&#xD;
hydroxycitric acid (HCA), an important biological active plant metabolite used as&#xD;
an anti-obesity drug. The female plants are the major source of main isomer, (-)&#xD;
- hydroxycitric acid, a powerful inhibitor of citrate cleavage enzyme. &lt;i&gt;G&lt;/i&gt;.&#xD;
&lt;i&gt;indica &lt;/i&gt;being a polygamodioecious sp, differentiation between male and female&#xD;
plants is detected only at the flowering stage (approx. 7 yrs). Tissue culture&#xD;
methods, offer scope for large scale&#xD;
&#xD;
propagation of female plants. An efficient&#xD;
protocol for multiple shoots and callus has been standardized to produce HCA.&#xD;
Multiple shoots were obtained from immature seed explants on MS basal medium supplemented&#xD;
with NAA (2.69 μ&lt;i&gt;M&lt;/i&gt;), BAP (8.9 μ&lt;i&gt;M&lt;/i&gt;) and KN (0.93 μ&lt;i&gt;M&lt;/i&gt;). Elongation&#xD;
of shoots was achieved on half MS medium supplemented with NAA&#xD;
&#xD;
(0.54 μ&lt;i&gt;M&lt;/i&gt;), BAP (0.44 μ&lt;i&gt;M&lt;/i&gt;) and&#xD;
KN (0.93 μ&lt;i&gt;M&lt;/i&gt;). The shoots developed roots when they were treated with&#xD;
4900 μ&lt;i&gt;M&lt;/i&gt; IBA for 30 seconds and cultured on half MS basal medium.&#xD;
Multiple&#xD;
&#xD;
shoots and callus were obtained from&#xD;
explants derived from &lt;i&gt;in vitro &lt;/i&gt;developed plantlets. The regenerated&#xD;
plantlets were&lt;i&gt; &lt;/i&gt;successfully transferred to soil in pots. Multiple shoots&#xD;
and the&#xD;
&#xD;
callus cultures produced HCA.
Page(s): 301-304</summary>
    <dc:date>2002-07-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;i&gt;Agrobacterium-mediated &lt;/i&gt;Transformation of Lucerne (&lt;i&gt;Medicago sativa &lt;/i&gt;Linn.): Optimizing Biological and Physical Parameters</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19879" />
    <author>
      <name>Kumar, Suresh</name>
    </author>
    <author>
      <name>Bhat, Vishnu</name>
    </author>
    <author>
      <name>Bhat, B V</name>
    </author>
    <author>
      <name>Gupta, M G</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19879</id>
    <updated>2013-07-20T16:33:34Z</updated>
    <published>2002-07-01T00:00:00Z</published>
    <summary type="text">Title: &lt;i&gt;Agrobacterium-mediated &lt;/i&gt;Transformation of Lucerne (&lt;i&gt;Medicago sativa &lt;/i&gt;Linn.): Optimizing Biological and Physical Parameters
Authors: Kumar, Suresh; Bhat, Vishnu; Bhat, B V; Gupta, M G
Abstract: An optimized protocol for the&#xD;
transformation of Indian cultivars of lucerne (&lt;i&gt;Medicago sativa &lt;/i&gt;Linn.)&#xD;
using &lt;i&gt;Agrobacterium tumefaciens &lt;/i&gt;has been developed. It involved a selectable&#xD;
marker gene encoding hygromycin phosphotransferase (&lt;i&gt;hpt &lt;/i&gt;II) which&#xD;
confers resistance to the&#xD;
&#xD;
antibiotic hygromycin, together with a reporter&#xD;
gene (&lt;i&gt;uid &lt;/i&gt;A) encoding P-D glucuronidase (GUS); cotyledonary and hypocotyl&#xD;
explants from &lt;i&gt;in vitro &lt;/i&gt;grown 5 days-old seedlings&#xD;
&#xD;
raised from mature seeds of genotype L-2&#xD;
and IL-75 as target tissues, and co-cultivation of explants with &lt;i&gt;A. tumefaciens&#xD;
&lt;/i&gt;strain LBA-4404 harbouring plasmid pCAMBIA-1301.&#xD;
&#xD;
Cotyledonary explant was found to be more&#xD;
responsive for transformation. Bacterial density of 5×10&lt;sup&gt;9&lt;/sup&gt; cells/ml&#xD;
and co-cultivation for three days were found to be most effective for stable&#xD;
GUS expression in 91 % of the hygromycin-resistant calli.
Page(s): 298-300</summary>
    <dc:date>2002-07-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Comparison of ELISA and GC Methods to Detect DDT Residues in Water Samples</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19878" />
    <author>
      <name>Amitarani, B E</name>
    </author>
    <author>
      <name>Pasha, Akmal</name>
    </author>
    <author>
      <name>Gowda, Putte</name>
    </author>
    <author>
      <name>Nagendraprasad, T R</name>
    </author>
    <author>
      <name>Karanth, N G K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19878</id>
    <updated>2013-07-23T16:32:59Z</updated>
    <published>2002-07-01T00:00:00Z</published>
    <summary type="text">Title: Comparison of ELISA and GC Methods to Detect DDT Residues in Water Samples
Authors: Amitarani, B E; Pasha, Akmal; Gowda, Putte; Nagendraprasad, T R; Karanth, N G K
Abstract: ELISA and GC methods were used to analyse&#xD;
DDT residues in about 30 water samples collected from different talukas of&#xD;
Mandya District of Karnataka. Polyclonal antibody based immunoassay developed at&#xD;
CFTRI, Mysore, performed&#xD;
well to detect the DDT residues. The minimum detectable level of DDT by ELISA was&#xD;
one part per billion (ppb) in the water samples tested. The insecticide residue&#xD;
ranged from 1 to 20 ppb. Experiments also revealed no matrix effect and hence&#xD;
did not require any prior clean-up. The &lt;i&gt;p&lt;/i&gt;H&lt;i&gt; &lt;/i&gt;of the water did not&#xD;
interfere in the assay. The ELISA method validated in the present work is specific&#xD;
to DDT. The results of ELISA with respect to DDT residues were found to be&#xD;
comparable to values obtained from the GC analysis of the water samples. The&#xD;
water samples could be directly used for ELISA test, thereby making the analysis&#xD;
quick, simple and cost effective.
Page(s): 292-297</summary>
    <dc:date>2002-07-01T00:00:00Z</dc:date>
  </entry>
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