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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/29316">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/29316</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/29339" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/29338" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/29337" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/29336" />
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    <dc:date>2026-10-10T18:26:44Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/29339">
    <title>Production of biocontrol traits by banana field fluorescent Pseudomonads and comparison with chemical fungicide</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/29339</link>
    <description>Title: Production of biocontrol traits by banana field fluorescent Pseudomonads and comparison with chemical fungicide
Authors: Shaikh, S S; Patel, P R; Patel, S S; Nikam, S D; Rane, T U; Sayyed, R Z
Abstract: &lt;i style="mso-bidi-font-style:normal"&gt;Pseudomonas&lt;/i&gt;&#xD;
&lt;i style="mso-bidi-font-style:normal"&gt;aeruginosa &lt;/i&gt;isolated from banana field&#xD;
rhizosphere produced different antifungal metabolites like bactriocin, hydrogen&#xD;
cyanide and siderophore. Bacteriocinogenic, siderophoregenic, and HCN rich&#xD;
broth of isolate inhibited the growth of phytopathogen like &lt;i style="mso-bidi-font-style:normal"&gt;Aspergilus niger, Aspergilus flavus, Fusarium&#xD;
oxysporum&lt;/i&gt; and &lt;i style="mso-bidi-font-style:normal"&gt;Alternaria alternata&lt;/i&gt;.&#xD;
&lt;span style="mso-bidi-font-weight:bold"&gt;The isolate exhibited more&#xD;
antifungal activity and comparatively low MIC vis-a-vis commonly used copper&#xD;
based systemic chemical fungicide;bil cop.&#xD;
&#xD;
&lt;/span&gt;
Page(s): 917-920</description>
    <dc:date>2014-09-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/29338">
    <title>&lt;i&gt;In vitro&lt;/i&gt; regeneration in &lt;span style="mso-bidi-font-weight:bold"&gt;olive (&lt;i style="mso-bidi-font-style:normal"&gt;Olea europaea&lt;/i&gt; L.) cv, ‘Frontio&lt;span style="mso-bidi-font-weight:bold"&gt;’ from nodal segments &lt;/span&gt;&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/29338</link>
    <description>Title: &lt;i&gt;In vitro&lt;/i&gt; regeneration in &lt;span style="mso-bidi-font-weight:bold"&gt;olive (&lt;i style="mso-bidi-font-style:normal"&gt;Olea europaea&lt;/i&gt; L.) cv, ‘Frontio&lt;span style="mso-bidi-font-weight:bold"&gt;’ from nodal segments &lt;/span&gt;&lt;/span&gt;
Authors: Mangal, Manisha; Sharma, Dheeraj; Sharma, Mamta; Kumar, Sunil
Abstract: An efficient and reproducible protocol for&#xD;
plantlet regeneration from nodal segments of Olive cv ‘Frontio’ has been&#xD;
developed. Media and explants browning due to exudation of phenolics from the&#xD;
explants were controlled by fortification of the medium with 100 mg/L ascorbic&#xD;
acid. Best establishment of olive explants was observed on half-strength MS&#xD;
salts fortified with 2.0 mg/L 6-benzylaminopurine (BAP), which resulted in&#xD;
56.2% of bud break and 93.7% survival whereas, a combination of full strength&#xD;
MS medium with 1.0 mg/L each of 3-indole-butyric-acid (IBA) and kinetin was&#xD;
found to be the best for shoot multiplication, in terms of number of shoots&#xD;
(3.6 shoots/explant) and shoot length (2.2 cm). The &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;in vitro&lt;/i&gt; shoots were rooted on half-strength MS medium fortified&#xD;
with 0.2 mg/L IBA and 0.2 mg/L α-naphthalene&#xD;
acetic acid (NAA) with 1.5 g/L activated charcoal, which supported optimum&#xD;
rooting (60 %), with an average of 2-3 roots/shoot, about 2.4 cm length were&#xD;
produced on four weeks of culture.
Page(s): 912-916</description>
    <dc:date>2014-09-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/29337">
    <title>Mass propagation of &lt;i style="mso-bidi-font-style:normal"&gt;Cymbidium giganteum &lt;/i&gt;Wall. ex Lindl. using &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;/i&gt; seedlings</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/29337</link>
    <description>Title: Mass propagation of &lt;i style="mso-bidi-font-style:normal"&gt;Cymbidium giganteum &lt;/i&gt;Wall. ex Lindl. using &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;/i&gt; seedlings
Authors: Ghosh, Amrita; Hossain, M Musharof; Sharma, Madhu
Abstract: &lt;i style="mso-bidi-font-style:normal"&gt;In&#xD;
vitro&lt;/i&gt; seedlings were used as explants for protocorm&#xD;
like bodies (PLBs) production which in turn were used for regeneration purpose.&#xD;
PLBs were induced from the base of seedlings (1.0-1.5 cm in size) in MS + BAP&#xD;
(8.88 µM). After 90 days of inoculation, PLBs production rate started declining&#xD;
and most of the PLBs turned into plantlets. Preculture of seedlings in 1.0 µM thidiazuron&#xD;
(TDZ) for 7 days and transfer to BAP supplemented medium resulted in production&#xD;
of 16 PLBs per seedling within 90 days of culture. Increase of TDZ&#xD;
concentration to 2.5 µM and preculture time 15 days, resulted in induction of&#xD;
highest number of PLBs (19 PLBs per seedling) in the basal medium. The results&#xD;
emphasized the importance of thidiazuron (TDZ) concentration and preculture&#xD;
time for PLBs proliferation from the base of seedlings. The PLBs thus produced&#xD;
were used for regeneration studies. Irrespective of single, segmented or clumps&#xD;
of PLBs, the regeneration response was 100% in 2,4-D (4.52 µM) and KN (4.64 µM)&#xD;
but when KN was replaced by BAP (8.88 µM), response was observed only in clumps&#xD;
of PLBs, whereas in single and segmented ones it was 99 and 97%, respectively.&#xD;
Regenerants developed stout root system in half strength M medium supplemented&#xD;
with 2.84 µM of IAA and transferred to greenhouse with 90% survival. T&lt;span style="mso-fareast-font-family:AdvP4DF60E;mso-ansi-language:EN-US" lang="EN-US"&gt;he&#xD;
present &lt;span style="mso-fareast-font-family:AdvP4DF60E;mso-ansi-language:EN-US" lang="EN-US"&gt;study&#xD;
holds tremendous potential as the mother plant is not destroyed and PLBs are produced as a&#xD;
continuous system.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;
Page(s): 905-911</description>
    <dc:date>2014-09-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/29336">
    <title>Chloroplast ultra structure, photosynthesis and enzyme activities in regenerated plants of &lt;i style="mso-bidi-font-style: normal"&gt;Stevia rebaudiana&lt;/i&gt; (Bert.) Bertoni as influenced by copper sulphate in the medium</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/29336</link>
    <description>Title: Chloroplast ultra structure, photosynthesis and enzyme activities in regenerated plants of &lt;i style="mso-bidi-font-style: normal"&gt;Stevia rebaudiana&lt;/i&gt; (Bert.) Bertoni as influenced by copper sulphate in the medium
Authors: Jain, Pourvi; Kachhwaha, Sumita; Kothari, S L
Abstract: &lt;i style="mso-bidi-font-style:normal"&gt;Stevia&#xD;
rebaudiana &lt;/i&gt;(Bert.)&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt; &lt;/i&gt;Bertoni is an important medicinal plant used as noncaloric&#xD;
commercial sweetener. Plants regenerated&lt;i style="mso-bidi-font-style:normal"&gt; &lt;/i&gt;with&#xD;
higher levels of copper sulphate in the medium exhibited enhanced activity of&#xD;
peroxidase and polyphenoloxidase (PPO) enzymes. Transmission electron&#xD;
microscopy (TEM) revealed increase in size and number of electron dense&#xD;
inclusions in the chloroplasts of plants regenerated at optimised level of&#xD;
copper sulphate (0.5µM) in the medium. There was decrease in chlorogenic acid&#xD;
(CGA) content. Chl-a-fluorescence transient pattern (OJIP) showed that the&#xD;
photosynthesis process was more efficient at 0.5µM CuSO&lt;sub&gt;4 &lt;/sub&gt;in the&#xD;
medium.&amp;nbsp;
Page(s): 898-904</description>
    <dc:date>2014-09-01T00:00:00Z</dc:date>
  </item>
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