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The β-galactosidase-encodingbgaM gene ofBacillus megaterium DSM319 and the divergently orientatedbgaR operon were isolated and sequenced. Both traits are subject to catabolite repression. A set of single-gene replacement mutants was generated and used to analyze gene function. BgaR was found to be a XylS/AraC-type positive transcriptional regulator ofbgaM ; a potential regulator binding site overlaps thebgaM promoter. A mechanism for regulation of β-galactosidase expression inB. megaterium is proposed.

Regulation of β-Galactosidase Expression in Bacillus megaterium DSM319 by a XylS/AraC-Type Transcriptional Activator