Gc. Shaw et al., CLONING, EXPRESSION, AND CATABOLITE REPRESSION OF A GENE ENCODING BETA-GALACTOSIDASE OF BACILLUS-MEGATERIUM ATCC-14581, Journal of bacteriology, 180(17), 1998, pp. 4734-4738
A gene encoding beta-galactosidase, designated mbgA, was isolated from
Bacillus megaterium ATCC 14581, Chromosomal beta-galactosidase produc
tion could be dramatically induced by lactose but not by isopropyl-bet
a-D-thiogalactopyranoside (IPTG) and was subject to catabolite repress
ion by glucose. Disruption of mbgA in the B. megaterium chromosome res
ulted in loss of lactose-inducible beta-galactosidase production. A 27
-bp inverted repeat was found to overlap the mbgA promoter sequence. T
wo partially overlapping catabolite-responsive elements (CREs) were id
entified within the inverted repeat. Base substitutions within CRE-I a
nd/or CRE-II caused partial relief from catabolite repression. The res
ults suggest that the 27-bp inverted repeat may serve as a target for
a catabolite repressor(s).