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Cloning and Characterization of Serine Protease Inhibitor Genes (SPIs) From Plants

KrishiKosh

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Title Cloning and Characterization of Serine Protease Inhibitor Genes (SPIs) From Plants
 
Creator D.A.Shirani
 
Contributor Sumangala Bhat
 
Subject Plant Bio-Technology
 
Description Plant serine protease inhibitors (SPIs) can be effective in developing
transgenic crop plants with resistance to insect attack. Such genes have few problems
related to codon bias, RNA processing and protein stability.
In the present study, an attempt was made to clone serine protease inhibitor
genes from soybean (Glycine max), cowpea (Vigna unguiculata) and yard long bean
(Vigna sesquipedalis). Using specific primers, genes encoding kunitz trypsin inhibitor
of soybean (SKTI) and cowpea trypsin inhibitor (CpTI) from cowpea and yard long
bean were amplified and cloned into pTZ57R/T vector. The clones were confirmed
through PCR amplification and restriction digestion analysis. Further, the clones were
sequenced and analyzed in silico.
Cloned kunitz trypsin inhibitor of soybean showed 99 and 100 per cent
homology with reported kunitz inhibitor genes of soybean at nucleotide and protein
level respectively. The cloned CpTI of cowpea and yard long bean showed 99%
homology with Phaseolus vulgaris trypsin proteinase inhibitor gene and published
CpTI coding sequences (324bp). The deduced amino acid sequence of cloned cowpea
CpTI showed 100% homology with Phaseolus vulgaris trypsin inhibitor whereas
CpTI of yard long bean showed 98 percent homology.
Further, to facilitate transformation of crop plants, soybean kunitz trypsin
inhibitor and CpTI of cowpea and yard long bean were sub cloned into a plant
transformation vector pHS100 at BamH1 and Xba1 restriction sites. The recombinant
clones pHS-SBC1, pHS-CpC1 and pHS-YLBC3 were mobilized into Agrobacterium
tumefaciens LBA4404 by triparental mating. The A. tumefaciens with recombinant
clones pHS-SBC1 and pHS-CpC1 were used to transform tobacco and the presence of
inserts in kanamycin resistant plants was checked through PCR with specific primers.
The events have to be confirmed further and expression tested.
 
Date 2016-10-17T13:33:46Z
2016-10-17T13:33:46Z
2005
 
Type Thesis
 
Identifier http://krishikosh.egranth.ac.in/handle/1/80703
 
Format application/pdf
 
Publisher UAS, Dharwad