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Applied and Environmental Microbiology, August 2002, p. 4132-4135, Vol. 68, No. 8
0099-2240/02/$04.00+0 DOI: 10.1128/AEM.68.8.4132-4135.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
FSW
Institute of Microbiology and Genetics, Vienna Biocenter, University of Vienna, 1030 Vienna, Austria,1 Department of Biology, University of Kaiserslautern, 67653 Kaiserslautern, Germany2
Received 20 December 2001/ Accepted 29 April 2002
With the aim to extend the presently available inducible gene expression systems for lactobacilli, we have isolated a thermoinducible promoter-repressor cassette from the temperate Lactobacillus casei phage
FSW-TI in Escherichia coli. The
FSW-TI promoter fragment was abutted to the plasmid-borne promoterless ß-glucuronidase (gusA) reporter gene and shown to direct its transcription in L. casei. In addition, the functionality of the promoter-repressor system was verified in the L. casei
FSW-TI lysogen by showing that the gusA reporter gene, controlled by the isolated
FSW-TI promoter, was repressed at 28°C and expressed at 42°C. Moreover, a homology search revealed that the C terminus of the isolated
FSW repressor shows a high similarity to the small mutS-related domain of the MutS2 protein family that is unprecedented for phage-encoded repressor proteins.
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