Construction of a Bile-responsive Expression System in .

Food Sci Anim Resour

Department of Animal Resources Science, Dankook University, Cheonan 31116, Korea.

Published: February 2019

This study aimed to develop a bile-responsive expression system for lactobacilli. The promoters of four genes, encoding phosphoenolpyruvate-dependent sugar phosphotransferase (mannose-specific), L-lactate dehydrogenase (LDH), HPr kinase, and D-alanine-D-alanine ligase, respectively, which were highly expressed by bile addition in PF01, were chosen. Each promoter was amplified by polymerase chain reaction and fused upstream of the β-glucuronidase gene as a reporter, respectively. Then, these constructs were cloned into - shuttle vector pULP2, which was generated by the fusion of pUC19 with the plasmid pLP27. Finally, the constructed vectors were introduced into for a promoter activity assay. The LDH promoter showed the highest activity and its activity increased 1.8-fold by bile addition. The constructed vector maintained in until 80 generations without selection pressure. A bile-responsive expression vector, pULP3-P, for spp. can be an effective tool for the bile-inducible expression of bioactive proteins in intestine after intake in the form of fermented dairy foods.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413156PMC
http://dx.doi.org/10.5851/kosfa.2018.e58DOI Listing

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