J Bacteriol, May 1998, p. 2273-2279, Vol. 180, No. 9
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Mikrobielle Genetik, Universität Tübingen, D-72076 Tübingen, Germany
Received 14 November 1997/Accepted 3 March 1998
The lactose utilization genes of Staphylococcus xylosus
have been isolated and characterized. The system is comprised of two structural genes, lacP and lacH, encoding the
lactose permease and the
-galactosidase proteins, respectively, and
a regulatory gene, lacR, coding for an activator of the
AraC/XylS family. The lactose utilization genes are divergently
arranged, the lacPH genes being opposite to
lacR. The lacPH genes are cotranscribed from
one promoter in front of lacP, whereas lacR is
transcribed from two promoters of different strengths. Lactose
transport as well as
-galactosidase activity are inducible by the
addition of lactose to the growth medium. Primer extension experiments demonstrated that regulation is achieved at the level of
lacPH transcription initiation. Inducibility and efficient
lacPH transcription are dependent on a functional
lacR gene. Inactivation of lacR resulted in low
and constitutive lacPH expression. Expression of
lacR itself is practically constitutive, since
transcription initiated at the major lacR promoter does not
respond to the availability of lactose. Only the minor lacR
promoter is lactose inducible. Apart from lactose-specific,
LacR-dependent control, the lacPH promoter is also subject
to carbon catabolite repression mediated by the catabolite control
protein CcpA. When glucose is present in the growth medium,
lacPH transcription initiation is reduced. Upon
ccpA inactivation, repression at the lacPH
promoter is relieved. Despite this loss of transcriptional regulation
in the ccpA mutant strain,
-galactosidase activity is
still reduced by glucose, suggesting another level of control.
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