RAPD Analysis TO Assess the Genetic Stability in Tissue Culture Derived Black Pepper Plants
By: Haneesh Babu T P.
Contributor(s): Nazeem P A (Guide).
Material type:
BookPublisher: Vellanikkara Department Of Plantation Crops And Spices,College Of Horticulture 2000DDC classification: 633.8 Online resources: Click here to access online Dissertation note: MSc 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.
| Item type | Current location | Call number | Status | Date due | Barcode |
|---|---|---|---|---|---|
Theses
|
KAU Central Library, Thrissur Theses | 633.8 HAN/RA (Browse shelf) | Available | 171648 |
MSc
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.
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