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J. Bacteriol., Jan 1997, 228-234, Vol 179, No. 1
M Geanacopoulos and S Adhya
An isorepressor of the gal regulon in Escherichia coli, GalS, has been
purified to homogeneity. In vitro DNase I protection experiments indicated
that among operators of the gal regulon, GalS binds most strongly to the
external operator of the mgl operon, which encodes the high-affinity
beta-methylgalactoside galactose transport system, and with less affinity
to the operators controlling expression of the gal operon, which codes for
enzymes of galactose metabolism. GalS has even less affinity for the
external operator of galP, which codes for galactose permease, the major
low-affinity galactose transporter in the cell. This order of affinities is
the reverse of that of GalR, which binds most strongly to the operator of
galP and most weakly to that of mgl. Our results also show that GalS, like
its homolog, GalR, is a dimeric protein which in binding to the bipartite
operators of the gal operon selectively represses its P1 promoter.
Consistent with the fact that GalR is the exclusive regulator of the
low-affinity galactose transporter, galactose permease, and that the major
role of GalS is in regulating expression of the high-affinity galactose
transporter encoded by the mgl operon, we found that the DNA binding of
GalS is 15- fold more sensitive than that of GalR to galactose.
Copyright © 1997, American Society for Microbiology
Functional characterization of roles of GalR and GalS as regulators of the gal regulon
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4255, USA.
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