Affiliation:
1. Laboratoire GPMA, IFR92, ENSBANA Université de Bourgogne, 1 esplanade Erasme, F-21000 Dijon, France
Abstract
ABSTRACT
In
Bacillus subtilis
, several phenolic acids specifically induce expression of
padC
, encoding a phenolic acid decarboxylase that converts these antimicrobial compounds into vinyl derivatives.
padC
forms an operon with a putative coding sequence of unknown function,
yveFG
, and this coding sequence does not appear to be involved in the phenolic acid stress response (PASR). To identify putative regulators involved in the PASR, random transposon mutagenesis, combined with two different screens, was performed. PadR, a negative transcriptional regulator of
padC
expression, was identified.
padR
is not located in the vicinity of
padC
, and the expression of
padR
is low and appears constitutive. This is in contrast with what occurs in other gram-positive bacteria, in which
padR
is autoregulated and induced by phenolic acids. Further screening of the transposon library failed to identify genes other than
padR
involved in the PASR. Modest inactivation of
padR
by phenolic acids was obtained in recombinant
Escherichia coli
expressing
padC
and
padR
, and this translates into induction of decarboxylase activity. Gel shift promoter binding assays performed with and without MgCl
2
, and with and without phenolic acids, demonstrated that phenolic acids were able to abolish the binding of PadR to the
yveFG
-
padC
promoter in the absence of MgCl
2
. Altogether, our results indicate that (i) PadR is inactivated directly by phenolic acids in vitro, (ii) inhibition of PadR in response to phenolic acids may occur without the need for a sensor-like effector in
B. subtilis
, and (iii) phenolic acids are able to modulate PadR activity in
E. coli
in the absence of any additional effector.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
62 articles.
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