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A gene encoding β-galactosidase, designatedmbgA , was isolated fromBacillus megaterium ATCC 14581. Chromosomal β-galactosidase production could be dramatically induced by lactose but not by isopropyl-β-d -thiogalactopyranoside (IPTG) and was subject to catabolite repression by glucose. Disruption ofmbgA in theB. megaterium chromosome resulted in loss of lactose-inducible β-galactosidase production. A 27-bp inverted repeat was found to overlap thembgA promoter sequence. Two partially overlapping catabolite-responsive elements (CREs) were identified within the inverted repeat. Base substitutions within CRE-I and/or CRE-II caused partial relief from catabolite repression. The results suggest that the 27-bp inverted repeat may serve as a target for a catabolite repressor(s).

Cloning, Expression, and Catabolite Repression of a Gene Encoding β-Galactosidase of Bacillus megaterium ATCC 14581