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Published 2003

Read in Norwegian

Publication details

Journal : Letters in Applied Microbiology , vol. 31 , p. 115–120 , 2003

International Standard Numbers :
Printed : 0266-8254
Electronic : 1472-765X

Publication type : Academic article

Contributors : Axelsson, Lars; Lindstad, G.; Naterstad, Kristine

If you have questions about the publication, you may contact Nofima’s Chief Librarian.

Kjetil Aune
Chief Librarian
kjetil.aune@nofima.no

Summary

Aim: To develop an inducible gene expression system for Lactobacillus sakei, based on the regulatory system of sakacin A production.

Methods and Results: A Lactobacillus/Escherichia coli shuttle vector; pKRV3, was constructed including the signal transducing system genes of the bacteriocin sakacin A. The gusA gene fused to PsapA promoter, cloned in this vector allowed for inducible beta-glucuronidase expression in L. sakei and L. plantarum following the addition of the sakacin A inducing peptide. PsapA appeared to be a strong and tightly controlled promoter when compared with known promoters.

Conclusion: The pKRV3 system can be used as an inducible gene expression system in lactobacilli.

Significance and Impact of the Study: A novel, inducible gene expression system has been developed for lactic acid bacteria relevant in food fermentations.

Contacts: