Regulation of fatty acid biosynthesis by the global regulator C cp A and the local regulator F ab T in S treptococcus mutans
SMU .1745c, encoding a putative transcriptional regulator of the M ar R family, maps to a location proximal to the fab gene cluster in S treptococcus mutans . Deletion of the SMU .1745c ( fab T S m ) coding region resulted in a membrane fatty acid composition comprised of longer‐chained, unsaturated...
Saved in:
Published in: | Molecular oral microbiology Vol. 30; no. 2; pp. 128 - 146 |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-04-2015
|
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | SMU
.1745c, encoding a putative transcriptional regulator of the
M
ar
R
family, maps to a location proximal to the
fab
gene cluster in
S
treptococcus mutans
. Deletion of the
SMU
.1745c (
fab
T
S
m
) coding region resulted in a membrane fatty acid composition comprised of longer‐chained, unsaturated fatty acids (
UFA
), compared with the parent strain. Previous reports have indicated a role for
F
ab
T
in regulation of genes in the
fab
gene cluster in other organisms, through binding to a palindromic
DNA
sequence. Consensus
F
ab
T
motif sequences were identified in
S
. mutans
in the intergenic regions preceding
fab
M
,
fab
T
Sm
and
fab
K
in the
fab
gene cluster. Chloramphenicol acetyltransferase (
cat
) reporter fusions, using the
fab
M
promoter, revealed elevated transcription in a ∆
fab
T
S
m
background. Transcription of
fab
T
S
m
was dramatically elevated in cells grown at p
H
values of 5 and 7 in the ∆
fab
T
S
m
background. Transcription of
fab
T
S
m
was also elevated in a strain carrying a deletion for the carbon catabolite repressor
C
cp
A
. Purified
F
ab
T
S
m
and
C
cp
A
bound to the promoter regions of
fab
T
S
m
and
fab
M
. Hence, the data indicate that
F
ab
T
S
m
acts as a repressor of
fab
M
and
fab
T
S
m
itself and the global regulator
C
cp
A
acts as a repressor for
fab
T
S
m
. |
---|---|
ISSN: | 2041-1006 2041-1014 |
DOI: | 10.1111/omi.12076 |