Transcriptional regulation of the rhaT gene, one of the operons formin
g the rhamnose regulon in Escherichia coli, was studied by fusing its
complete or deleted promoter to the reporter gene lacZ, Analysis of be
ta-galactosidase activities induced in these constructions grown under
different conditions predicted the presence of two putative control e
lements: one for the RhaS regulatory protein and activating the gene n
ot only by L-rhamnose but also by L-lyxose or L-mannose, the other for
cAMP-catabolite repression protein and activating this gene in the ab
sence of glucose. Anaerobiosis increased the promoter function two- to
threefold with respect to the aerobic condition, Experiments involvin
g complementation of strains containing the rhaT-promoter fusion and c
arrying a deletion in the rhaS and/or rhaR genes with plasmids bearing
the rhamnose regulatory genes showed that rhaT is controlled by a reg
ulatory cascade, in which RhaR induces rhaSR and the accumulated RhaS
directly activates rhaT.