Affiliation:
1. Dipartimento di Biologia e Biotecnologie Lazzaro Spallanzani, Università di Pavia, Pavia, Italy
2. Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, USA
Abstract
ABSTRACT
AprE and NprE are two major extracellular proteases in
Bacillus subtilis
whose expression is directly regulated by several pleiotropic transcriptional factors, including AbrB, DegU, ScoC, and SinR. In cells growing in a rich, complex medium, the
aprE
and
nprE
genes are strongly expressed only during the post-exponential growth phase; mutations in genes encoding the known regulators affect the level of post-exponential-phase gene expression but do not permit high-level expression during the exponential growth phase. Using DNA-binding assays and expression and mutational analyses, we have shown that the genes for both exoproteases are also under strong, direct, negative control by the global transcriptional regulator CodY. However, because CodY also represses
scoC
, little or no derepression of
aprE
and
nprE
was seen in a
codY
null mutant due to overexpression of
scoC
. Thus, CodY is also an indirect positive regulator of these genes by limiting the synthesis of a second repressor. In addition, in cells growing under conditions that activate CodY, a
scoC
null mutation had little effect on
aprE
or
nprE
expression; full effects of
scoC
or
codY
null mutations could be seen only in the absence of the other regulator. However, even the
codY scoC
double mutant did not show high levels of
aprE
and
nprE
gene expression during exponential growth phase in a rich, complex medium. Only a third mutation, in
abrB
, allowed such expression. Thus, three repressors can contribute to reducing exoprotease gene expression during growth in the presence of excess nutrients.
IMPORTANCE
The major
Bacillus subtilis
exoproteases, AprE and NprE, are important metabolic enzymes whose genes are subject to complex regulation by multiple transcription factors. We show here that expression of the
aprE
and
nprE
genes is also controlled, both directly and indirectly, by CodY, a global transcriptional regulator that responds to the intracellular pools of amino acids. Direct CodY-mediated repression explains a long-standing puzzle, that is, why exoproteases are not produced when cells are growing exponentially in a medium containing abundant quantities of proteins or their degradation products. Indirect regulation of
aprE
and
nprE
through CodY-mediated repression of the
scoC
gene, encoding another pleiotropic repressor, serves to maintain a significant level of repression of exoprotease genes when CodY loses activity.
Funder
HHS | NIH | National Institute of General Medical Sciences
Università degli Studi di Pavia
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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