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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/2804" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/2804</id>
  <updated>2026-10-10T16:48:58Z</updated>
  <dc:date>2026-10-10T16:48:58Z</dc:date>
  <entry>
    <title>&lt;i style=""&gt;In vitro&lt;/i&gt; propagation of tikhur (&lt;i style=""&gt;Curcuma angustifolia&lt;/i&gt; Roxb.): A starch yielding plant</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/5140" />
    <author>
      <name>Shukla, S K</name>
    </author>
    <author>
      <name>Shukla, Susmita</name>
    </author>
    <author>
      <name>Koche, Vijaya</name>
    </author>
    <author>
      <name>Mishra, S K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/5140</id>
    <updated>2009-07-03T16:31:16Z</updated>
    <published>2007-04-01T00:00:00Z</published>
    <summary type="text">Title: &lt;i style=""&gt;In vitro&lt;/i&gt; propagation of tikhur (&lt;i style=""&gt;Curcuma angustifolia&lt;/i&gt; Roxb.): A starch yielding plant
Authors: Shukla, S K; Shukla, Susmita; Koche, Vijaya; Mishra, S K
Abstract: &lt;i style=""&gt;In vitro&lt;/i&gt; regeneration of &lt;i style=""&gt;Curcuma angustifolia&lt;/i&gt; Roxb. was achieved through shoot meristem culture&lt;i style=""&gt;. &lt;/i&gt;The shoot buds (2-3 cm long) from rhizome were inoculated on MS medium supplemented with 3.0 mg/L BAP for initiation and elongation of shoots. As a result, 1.87±0.28 shoots per explant were produced These shoots were transferred on MS medium supplemented with 3.0 mg/L BAP and 25 mg/L adenine sulfate for further shoot multiplication. About 6.9±0.69 micro-shoots per explant were produced with in 6 wk. The roots appeared from shoots on shoot establishment as well as multiplication media. The rooted plants were transferred to pots and acclimatized, which showed 83% survival with normal growth.&lt;b style=""&gt;&lt;/b&gt;
Page(s): 274-276</summary>
    <dc:date>2007-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Studies on flavonoid production using &lt;i style=""&gt;in vitro&lt;/i&gt; cultures of &lt;i style=""&gt;Momordica charantia &lt;/i&gt;L.</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/5122" />
    <author>
      <name>Agarwal, Mala</name>
    </author>
    <author>
      <name>Kamal, Raka</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/5122</id>
    <updated>2009-07-09T16:30:23Z</updated>
    <published>2007-04-01T00:00:00Z</published>
    <summary type="text">Title: Studies on flavonoid production using &lt;i style=""&gt;in vitro&lt;/i&gt; cultures of &lt;i style=""&gt;Momordica charantia &lt;/i&gt;L.
Authors: Agarwal, Mala; Kamal, Raka
Abstract: Callus cultures and &lt;i style=""&gt;in vitro &lt;/i&gt;plant development of &lt;i style=""&gt;Momordica charantia &lt;/i&gt;L&lt;i style=""&gt;.&lt;/i&gt; were establishment on Murashige and Skoog’s (MS) medium using different concentrations and combinations of auxins and cytokinins. Further, qualitative and quantitative production of flavonoids in callus cultures and different &lt;i style=""&gt;in vitro &lt;/i&gt;developmental stages were studied by using thin layer chromatography and spectrophotometric analysis. Presence of three flavonoids was detected and the maximum amount of total flavonoid content was observed in 6-wkold callus cultures (2.90 mg/g dry wt). While in different&lt;i style=""&gt; in vitro &lt;/i&gt;morphogenetic stages, the maximum amount of total flavonoid content was observed in multiple shoots (2.96 mg/g dry wt).&lt;b style=""&gt;&lt;/b&gt;
Page(s): 277-279</summary>
    <dc:date>2007-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Plant regeneration through somatic embryogenesis from stem and petiole explants of Indian chicory (&lt;i style=""&gt;Cichorium intybus&lt;/i&gt; L.)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/5120" />
    <author>
      <name>Abdin, M Z</name>
    </author>
    <author>
      <name>Ilah, A</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/5120</id>
    <updated>2009-07-04T16:30:47Z</updated>
    <published>2007-04-01T00:00:00Z</published>
    <summary type="text">Title: Plant regeneration through somatic embryogenesis from stem and petiole explants of Indian chicory (&lt;i style=""&gt;Cichorium intybus&lt;/i&gt; L.)
Authors: Abdin, M Z; Ilah, A
Abstract: An efficient protocol has been developed for rapid propagation of Indian chicory (&lt;i style=""&gt;Cichorium intybus L.&lt;/i&gt;) through somatic embryo development. Indirect somatic embryogenesis was induced through nodal stem and petiole explants, cultured on Murashige and Skoog (MS) medium containing different concentrations of 2,4-D, NAA or IAA. Callus was induced from both the explants after 3 wk of inoculation. Subsequently, calli were sub-cultured on MS medium containing different auxin/cytokinin ratios that influenced the intensity of embryo formation, germination and ability to regenerate plants. Somatic embryogenesis was more intensive in medium with higher concentration of Kn (1.5 mg L&lt;sup&gt;-1&lt;/sup&gt;) and lower concentration of IAA (0.5 mg L&lt;sup&gt;-1&lt;/sup&gt;) supplemented with vitamin-free casein hydrolysate (500 mg L&lt;sup&gt;-1&lt;/sup&gt;). After sub-culture, the embryoids were matured onto a fresh MS medium supplemented with Kn (1.5 mg L&lt;sup&gt;-1&lt;/sup&gt;) + IAA (0.1 mg L&lt;sup&gt;-1&lt;/sup&gt;) + IBA (1.0 mg L&lt;sup&gt;-1&lt;/sup&gt;) + CH (500 mg L&lt;sup&gt;-1&lt;/sup&gt;). The germination of embryos into shoots and less developed roots occurred on the same medium with slight change in IBB concentration (0.5 mg L&lt;sup&gt;-1&lt;/sup&gt;). Further, root formation occurred in MS medium supplemented with 1.0 mg L&lt;sup&gt;-1 &lt;/sup&gt;IBA.
Page(s): 250-255</summary>
    <dc:date>2007-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Effects of different culture media on seed germination and subsequent &lt;i style=""&gt;in vitro&lt;/i&gt; development of protocorms&lt;i&gt; &lt;/i&gt;of&lt;i&gt; Hygrochilus parishii &lt;/i&gt;(Veith &amp;&lt;i&gt; &lt;/i&gt;Rchb.f.) Pfitz (Orchidaceae)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/5103" />
    <author>
      <name>Shadang, R</name>
    </author>
    <author>
      <name>Dwivedi, Padmanabh</name>
    </author>
    <author>
      <name>Hegde, S N</name>
    </author>
    <author>
      <name>Ahmed, N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/5103</id>
    <updated>2009-07-06T16:30:30Z</updated>
    <published>2007-04-01T00:00:00Z</published>
    <summary type="text">Title: Effects of different culture media on seed germination and subsequent &lt;i style=""&gt;in vitro&lt;/i&gt; development of protocorms&lt;i&gt; &lt;/i&gt;of&lt;i&gt; Hygrochilus parishii &lt;/i&gt;(Veith &amp;&lt;i&gt; &lt;/i&gt;Rchb.f.) Pfitz (Orchidaceae)
Authors: Shadang, R; Dwivedi, Padmanabh; Hegde, S N; Ahmed, N
Abstract: Seeds of&lt;i&gt; Hygrochilus parishii&lt;/i&gt; (Veith &amp; Rchb.f.) Pfitz&lt;i&gt; &lt;/i&gt;were inoculated on eight different culture media (basal) MS, MKC, V&amp;W, I&amp;Y and half strength of respective media. Seeds germinated within 15-20 d almost on all media with varying percentage and developed into greenish protocorm after 80-100 d. Best seed germination was observed in ½ strength MKC medium. Healthy protocorms were observed within 100 d in V&amp;W media. Sub-cultured protocorms in all the above media supplemented with NAA, BAP, 2,4-D and IAA in a range of 0.5-2.0 mg L&lt;sup&gt;-1&lt;/sup&gt;, both individually and in combination, and additives like banana pulp (BP, 10%) and coconut milk (CM, 15%) produced well developed callus. Multiplication of protocorms was best on ½ strength MS + NAA (2.0 mg L&lt;sup&gt;-1&lt;/sup&gt;). Formation of root and leaf was early in V&amp;W medium having CM (15%) and BP (10%) but without sucrose.
Page(s): 256-261</summary>
    <dc:date>2007-04-01T00:00:00Z</dc:date>
  </entry>
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