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  <titleInfo>
    <title>RAPD Analysis TO Assess the Genetic Stability in Tissue Culture Derived Black Pepper Plants</title>
  </titleInfo>
  <name type="personal">
    <namePart>Haneesh Babu T P</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Nazeem P A (Guide)</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">xx</placeTerm>
    </place>
    <place>
      <placeTerm type="text">Vellanikkara</placeTerm>
    </place>
    <publisher>Department Of Plantation Crops And Spices,College Of Horticulture</publisher>
    <dateIssued>2000</dateIssued>
    <dateIssued encoding="marc">9999</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">und</languageTerm>
  </language>
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  <abstract>As part of the Post Graduate programme in the Department of Plantation 
Crops and Spices, College of Horticulture, Vellanikkara experiments were 
conducted at the Centre for Plant Biotechnology and Molecular Biology, College of 
Horticulture, Vellanikkara during the period from 1997 to 1999; to standardise the 
method of DNA isolation and the protocol for RAPD analysis in- black pepper so as 
to assess the genetic stability and clonal fidelity of tissue culture derived black 
pepper plants. 
Three methods described by Dellaporta et at. (1983); Doyle- and Doyle 
(1987) and Rogers and Bendich (1994) were tried. Modification of these methods 
were tried to find out the effect of grinding the tissue in liquid N2 and use of jJ- 
mercapto ethanol. The method suggested by Rogers and Bendich (1994) was found 
better in terms of yield and quality of DNA. Grinding with liquid N2 and use of jJ~ 
mercapto ethanol was found effective. Tender leaves were found to be the best 
source for recovery of quality DNA. 
Different levels and possible combinations of dNTPs, primer and enzyme 
were tried to standardise optimum levels of reaction components for RAPD analysis 
of black pepper. Best thermal cycle was identified for the amplification of black 
pepper genomic DNA. Different concentration of template DNA tried was found 
not influencing the amplification pattern. 
Sixty decarner primers were screened for amplification of black pepper 
genomic DNA. Ten primers selected for good amplification were used to screen five 
varieties of black pepper. Three primers, which showed polymorphism and stability 
of amplification, were used for analysis of TC plants. 
Tissue culture regenerants derived by bud culture were subjected to 
RAPD analysis using three primers (OPP-l, OPP-8, OPP-14). All the regenerants 
 
studied gave a uniform RAPD profile except in two regenerants where there was 
difference in expression of two non-distinct bands. 
The present study was effective in optimizing the protocol for RAPD 
analysis in black pepper and is the first of its kind reported in this valuable spice 
crop. The primers identified for varietal screening and the RAPD profile developed 
for the five important varieties can be utilised for fingerprinting of these varieties. 
The results also ensure the genetic stability and clonal fidelity of the TC plants and 
the suitability of tissue culture protocol for commercialisation. 

</abstract>
  <note>MSc</note>
  <classification authority="ddc">633.8 HAN/RA</classification>
  <identifier type="uri">http://krishikosh.egranth.ac.in/handle/1/5810104116</identifier>
  <location>
    <url>http://krishikosh.egranth.ac.in/handle/1/5810104116</url>
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    <recordCreationDate encoding="marc">140128</recordCreationDate>
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