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Originally published In Press as doi:10.1074/jbc.M103033200 on July 27, 2001
J. Biol. Chem., Vol. 276, Issue 40, 37060-37068, October 5, 2001
Superimposed Levels of Regulation of the 4-Hydroxyphenylacetate
Catabolic Pathway in Escherichia coli*
Beatriz
Galán ,
Annie
Kolb§,
José L.
García , and
María A.
Prieto ¶
From the Department of Molecular Microbiology, Centro
de Investigaciones Biológicas, Consejo Superior de
Investigaciones Científicas, Madrid 28006, Spain and
§ Laboratoire des Régulations Transcriptionnelles,
Institut Pasteur, 75724 Paris, Cedex 15, France
The regulation of the Pg promoter,
which controls the expression of the meta operon of the
4-hydroxyphenylacetic acid (4-HPA) catabolic pathway of
Escherichia coli W, has been examined through in
vivo and in vitro experiments. By using
Pg-lacZ fusions we have demonstrated that Pg is
a promoter only inducible in the stationary phase when cells are grown
on glucose as the sole carbon and energy source. This strict catabolite
repression control is mediated by the cAMP receptor protein (CRP). This
event does not require the presence of the specific HpaR repressor or
the 4-HPA permease (HpaX), excluding the involvement of a typical
inducer exclusion mechanism. However, the acetic acid excreted in the stationary phase by the cells growing in glucose acts as an overflow metabolite, which can provide the energy to produce cAMP and to adapt
the cells rapidly to the utilization of a new less preferred carbon
source such as the aromatic compounds. Although Pg is not a
38-dependent promoter, it is activated by
the global regulator integration host factor (IHF) in the stationary
phase of growth. Gel retardation assays have demonstrated that both CRP
and IHF simultaneously bind to the Pg upstream region.
DNase I footprint experiments showed that cAMP-CRP and IHF binding
sites are centered at 61.5 and 103, respectively, with respect to
the transcription start site +1 of the Pg promoter.
*
This work was supported by Comisión Interministerial
de Ciencia y Tecnología Grants ABM97-603-C02-02 and
BMC2000-0125-C04-02 and by the Program de Recherche Fondamentale en
Microbiologie, Maladies Infectieuses et Parasitaires.
¶
To whom correspondence should be addressed: Dept. of Molecular
Microbiology, Centro de Investigaciones Biológicas,
Velázquez 144, Madrid 28006, Spain. Tel.: 34-915611800; Fax:
34-915627518; E-mail: auxi@cib.csic.es.
Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2001 by the American Society for Biochemistry and Molecular Biology.
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