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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/33401" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/33401</id>
  <updated>2026-10-09T18:31:17Z</updated>
  <dc:date>2026-10-09T18:31:17Z</dc:date>
  <entry>
    <title>Enhancement in total lipids in microalgae through cultural manipulations and fatty acid profiling</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/33423" />
    <author>
      <name>Bagul, Samadhan</name>
    </author>
    <author>
      <name>Ratha, Sachitra Kumar</name>
    </author>
    <author>
      <name>Prasanna, Radha</name>
    </author>
    <author>
      <name>Saha, Supradip</name>
    </author>
    <author>
      <name>Dhar, Dolly Wattal</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/33423</id>
    <updated>2016-07-20T06:27:26Z</updated>
    <published>2015-07-01T00:00:00Z</published>
    <summary type="text">Title: Enhancement in total lipids in microalgae through cultural manipulations and fatty acid profiling
Authors: Bagul, Samadhan; Ratha, Sachitra Kumar; Prasanna, Radha; Saha, Supradip; Dhar, Dolly Wattal
Abstract: Three microalgal genera, namely, &lt;i&gt;Chlamydomonas&#xD;
&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt;sp., &lt;i&gt;Chlorococcum &lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt;sp. and &lt;i&gt;Chlorella &lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt;sp., were selected to optimize the&#xD;
environmental variables and cultural conditions for enhanced lipid production.&#xD;
Microalgae exhibited differential response in terms of total lipids under&#xD;
varied conditions of temperature, light, pH, salinity and nitrogen. &lt;i&gt;Chlorella&#xD;
&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt;sp. showed the highest&#xD;
lipid production in comparison to &lt;i&gt;Chlamydomonas &lt;/i&gt;&lt;span style="mso-bidi-font-style:&#xD;
italic"&gt;sp. and &lt;i style="mso-bidi-font-style:normal"&gt;Chlorococcum &lt;/i&gt;sp.&lt;span style="mso-bidi-font-weight:bold"&gt; Fatty acid profile indicated that &lt;i style="mso-bidi-font-style:normal"&gt;Chlorococcum &lt;/i&gt;sp. and &lt;i style="mso-bidi-font-style:normal"&gt;Chlorella&lt;/i&gt; sp. &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;w&lt;/i&gt;ere rich in array of fatty acids, which are suitable for biodiesel&#xD;
production.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 429-432</summary>
    <dc:date>2015-07-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:13.0pt;mso-bidi-font-size: 8.0pt" lang="EN-GB"&gt;Genetic uniformity analysis of cryopreseved&lt;i&gt; in vitro&lt;/i&gt; plantlets of &lt;i&gt;Kaempferia galanga&lt;/i&gt; L.—An endangered medicinal species in Tropical Asia &lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/33422" />
    <author>
      <name>Preetha, T S</name>
    </author>
    <author>
      <name>Kumar, A S Hemantha</name>
    </author>
    <author>
      <name>Padmesh, P</name>
    </author>
    <author>
      <name>Krishnan, P N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/33422</id>
    <updated>2016-07-20T06:26:44Z</updated>
    <published>2015-07-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="font-size:13.0pt;mso-bidi-font-size: 8.0pt" lang="EN-GB"&gt;Genetic uniformity analysis of cryopreseved&lt;i&gt; in vitro&lt;/i&gt; plantlets of &lt;i&gt;Kaempferia galanga&lt;/i&gt; L.—An endangered medicinal species in Tropical Asia &lt;/span&gt;
Authors: Preetha, T S; Kumar, A S Hemantha; Padmesh, P; Krishnan, P N
Abstract: While using the protocols for the long-term&#xD;
conservation, assessment of true-to-type regenerants from cryopreserved&#xD;
materials is important. In the present study, no significant variation in&#xD;
banding pattern was noticed in the RAPD profile of cryopreserved and control&#xD;
samples of shoot tip-derived&lt;i&gt; Kaempferia&#xD;
galanga&lt;/i&gt; plants. But&#xD;
in the case of somatic embryo-derived samples, some variation was observed in&#xD;
the banding pattern (16.2% polymorphism), though the plants were&#xD;
phenotypically similar. Recovery of cryopreserved somatic embryos in &lt;i&gt;K.&#xD;
galanga&lt;/i&gt; was preceded through a callus phase, from which secondary embryos&#xD;
were induced later. The RAPD profile of somatic&#xD;
embryo-derived samples revealed that variation was due to the occurrence&#xD;
of callus phase. As minor genetic variations arising in &lt;i&gt;in vitro &lt;/i&gt;cultures&#xD;
without marked phenotypic changes are considered to be beneficial for diversity&#xD;
conservation and sustainable utilization, cryopreserved somatic embryos of &lt;i&gt;K.&#xD;
galanga&lt;/i&gt; would serve as an alternative for generating and maintaining&#xD;
genetic diversity of this medicinal wealth.
Page(s): 425-428</summary>
    <dc:date>2015-07-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:13.0pt;mso-bidi-font-family:"Times New Roman"; mso-bidi-font-weight:bold" lang="EN-GB"&gt;Molecular assessment of genetic stability using ISSR and RAPD markers in &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;/i&gt; multiplied copies of commercial banana cv. Robusta &lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/33421" />
    <author>
      <name>Choudhary, D</name>
    </author>
    <author>
      <name>Kajla, S</name>
    </author>
    <author>
      <name>Poonia, A K</name>
    </author>
    <author>
      <name>Brar, B</name>
    </author>
    <author>
      <name>Surekha</name>
    </author>
    <author>
      <name>Duhan, J S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/33421</id>
    <updated>2016-07-20T06:26:10Z</updated>
    <published>2015-07-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="font-size:13.0pt;mso-bidi-font-family:"Times New Roman"; mso-bidi-font-weight:bold" lang="EN-GB"&gt;Molecular assessment of genetic stability using ISSR and RAPD markers in &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;/i&gt; multiplied copies of commercial banana cv. Robusta &lt;/span&gt;
Authors: Choudhary, D; Kajla, S; Poonia, A K; Brar, B; Surekha; Duhan, J S
Abstract: &lt;span style="font-size:9.0pt;mso-bidi-font-family:&#xD;
" times="" new="" roman""="" lang="EN-GB"&gt;The present study was carried out to monitor somaclonal&#xD;
variations of banana cv. Robusta during micropropagation using random amplified&#xD;
polymorphic DNA (RAPD) and inter simple sequence repeats (ISSR) markers. Shoot&#xD;
tips were used as explants and regenerated on MS+BAP 4.0 mg/L medium. The&#xD;
regenerated shoots were cultured on MS medium fortified with 4.0 mg/L BAP+0.25 mg/L&#xD;
NAA+30 mg/L AdSO&lt;sub&gt;4&lt;/sub&gt; for multiplication. Rooting was obtained on ½ MS&#xD;
medium supplemented with 2.0 mg/L NAA. Rooted shootlets were separated&#xD;
individually and hardened in greenhouse. The hardened plants of banana were&#xD;
screened for genetic stability using 46 &#xD;
(26 RAPD and 20 ISSR) primers. The number of scorable bands for each RAPD&#xD;
primer varied from 1 to 9. Twenty-six RAPD primers produced 108 distinct and&#xD;
scorable bands, with an average of 4.15 bands per primer and the amplification&#xD;
products range was from 100-1150 bps. No polymorphism was detected during the&#xD;
RAPD analysis of &lt;i&gt;i&lt;/i&gt;&lt;i style="mso-bidi-font-style:normal"&gt;n vitro &lt;/i&gt;raised&#xD;
clones. Twenty ISSR primers produced 81 distinct and scorable bands in the&#xD;
range of 100-1000 bps and the number of scorable bands for each primer varied&#xD;
from 2 to 8 with an average of 4.05 bands per primer. A homogenous&#xD;
amplification profile was observed for all the micropropagated plants when&#xD;
compared to mother plant in both types of markers used. The results corroborate&#xD;
the fact that &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;span style="mso-bidi-font-style:italic"&gt; &lt;/span&gt;&lt;/i&gt;multiplication is the safest&#xD;
mode for production of true to type plants.&#xD;
&#xD;
&lt;/span&gt;
Page(s): 420-424</summary>
    <dc:date>2015-07-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Molecular characterization of Assam  Local pig</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/33420" />
    <author>
      <name>Zaman, G</name>
    </author>
    <author>
      <name>Shekar, M Chandra</name>
    </author>
    <author>
      <name>Laskar, S</name>
    </author>
    <author>
      <name>Ferdoci, A M</name>
    </author>
    <author>
      <name>Rank, D N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/33420</id>
    <updated>2016-07-20T06:24:42Z</updated>
    <published>2015-07-01T00:00:00Z</published>
    <summary type="text">Title: Molecular characterization of Assam  Local pig
Authors: Zaman, G; Shekar, M Chandra; Laskar, S; Ferdoci, A M; Rank, D N
Abstract: The detailed genetic diversity of Assam&#xD;
Local pig population was studied through microsatellite markers. Most of the&#xD;
studied loci were polymorphic in nature and a total of 163 alleles were&#xD;
observed across all the loci. The range of alleles was found to be from 2 to 11&#xD;
with a mean of 6.52±2.311. The frequency distribution of microsatellite alleles&#xD;
in the population was from 0.0208 to 0.9091. The overall mean of observed and&#xD;
expected heterozygosities were 0.50±0.272 and 0.71±0.182, respectively. The polymorphism&#xD;
information content (PIC) was 0.67±0.184 and Shannon’s information index (I) was&#xD;
sufficiently high with a mean of 1.53. The within population inbreeding&#xD;
estimate (F&lt;sub&gt;IS&lt;/sub&gt;) value (0.273) indicated shortfall of heterozygosity&#xD;
in the population. The bottleneck analysis revealed that population had not undergone&#xD;
any recent reduction.
Page(s): 416-419</summary>
    <dc:date>2015-07-01T00:00:00Z</dc:date>
  </entry>
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