A system for efficient heterologous expression of class II bacteriocin
s is described that is based on introducing two plasmids in a bacterio
cin-negative Lactobacillus sake strain. The first plasmid (pSAK20) con
tains the genes necessary for transcriptional activation of the Sakaci
n A promoter as well as export and processing of bacteriocin precursor
s. The second plasmid (a pLPV111 derivative) contains the structural a
nd immunity genes for the bacteriocin of interest fused to the sakacin
A promoter. Using this system, various bacteriocins were produced at
levels equal to or higher than those obtained with the corresponding w
ild-type producer strains. (C) 1998 Published by Elsevier Science B.V.
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