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Cloning and expression of bovine casein cDNA

Posted on:2014-10-01Degree:M.ScType:Thesis
University:Stephen F. Austin State UniversityCandidate:Basak, SwarnaliFull Text:PDF
GTID:2453390005995323Subject:Biology
Abstract/Summary:
Eurygaster integriceps Puton (Sunn pest) causes major damage in wheat grains by injecting their saliva into the grain degrading the gluten proteins. This saliva protein has been identified and characterized as a prolyl endoprotease (spPEP) by (Darkoh et al. (2010). A natural, biological friendly inhibitor to the spPEP is being sought to protect the grains from the bug's attack and reduce grain loss. Previous studies have shown that casein peptides generated by Lactobacillis species have inhibitory effects on mammalian and bacterial prolyl endoproteases (PEP). The Objective of this study was to clone the four bovine casein genes, alpha1, alpha2, beta and kappa for use in expressing each isomer to identify which Lactobacillus generated peptides will inhibit the spPEP. The nucleotide sequences corresponding to bovine casein isomers were identified from the NCBI database to design gene specific primers that would amplify the full length casein proteins. Total RNA was extracted from bovine mammary gland biopsy tissue kindly donated by Dr. Erin Connor, Research Leader, USDA-ARS, Beltsville, MD and subsequent cDNA has been synthesized. Each casein subunit was cloned into the pGEM T-Easy vector for sequencing. Verified sequences were cloned into the pET28a E. coli expression vector for protein expression and purification using IMAC chromatography.
Keywords/Search Tags:Bovine casein, Expression
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