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Published on: June 12, 2019
Molecular characterization of the CmbR activator-binding site in the metC-cysK promoter region in Lactococcus lactis
Natasa Golic1,2,3, Martijn Schliekelmann2,3, María Fernández2,3
1Institute of Molecular Genetics and Genetic Engineering, Belgrade, Yugoslavia.
Abstract:
The metC-cysK operon involved in sulphur metabolism in Lactococcus lactis is positively regulated by the LysR-type protein CmbR. Transcription from the metC promoter is activated when concentrations of methionine and cysteine in the growth medium are low. The metC promoter region contains two direct and three inverted repeats. Deletion analysis indicated that direct repeat 2 (DR2) is required for activation of the metC promoter by CmbR. Gel mobility shift assays confirmed that CmbR binds to a 407 bp DNA fragment containing the metC promoter. This binding was stimulated by O-acetyl-L-serine. Competition experiments with deletion variants of the metC promoter showed that CmbR binding only occurred with fragments containing an intact DR2, confirming that DR2 is the CmbR binding site within the metC promoter.
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