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Acrylate reductase of an anaerobic electron transport chain of the marine bacterium Shewanella woodyi
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Many microorganisms are capable of anaerobic respiration in the absence of oxygen, by using different organic compounds as terminal acceptors in electron transport chain. We identify here an anaerobic respiratory chain protein responsible for acrylate reduction in the marine bacterium
Shewanella woodyi
. When the periplasmic proteins of
S. woodyi
were separated by ion exchange chromatography, acrylate reductase activity copurified with an ArdA protein (Swoo_0275). Heterologous expression of
S. woodyi ard
A gene (
swoo
_0275) in
Shewanella oneidensis
MR-1 cells did not result in the appearance in them of periplasmic acrylate reductase activity, but such activity was detected when the
ard
A gene was co-expressed with an
ard
B gene (
swoo
_0276). Together, these genes encode flavocytochrome
c
ArdAB, which is thus responsible for acrylate reduction in
S. woodyi
cells. ArdAB was highly specific for acrylate as substrate and reduced only methacrylate (at a 22-fold lower rate) among a series of other tested 2-enoates. In line with these findings, acrylate and methacrylate induced
ard
A gene expression in
S. woodyi
under anaerobic conditions, which was accompanied by the appearance of periplasmic acrylate reductase activity. ArdAB-linked acrylate reduction supports dimethylsulfoniopropionate-dependent anaerobic respiration in
S. woodyi
and, possibly, other marine bacteria.
Title: Acrylate reductase of an anaerobic electron transport chain of the marine bacterium
Shewanella woodyi
Description:
Many microorganisms are capable of anaerobic respiration in the absence of oxygen, by using different organic compounds as terminal acceptors in electron transport chain.
We identify here an anaerobic respiratory chain protein responsible for acrylate reduction in the marine bacterium
Shewanella woodyi
.
When the periplasmic proteins of
S.
woodyi
were separated by ion exchange chromatography, acrylate reductase activity copurified with an ArdA protein (Swoo_0275).
Heterologous expression of
S.
woodyi ard
A gene (
swoo
_0275) in
Shewanella oneidensis
MR-1 cells did not result in the appearance in them of periplasmic acrylate reductase activity, but such activity was detected when the
ard
A gene was co-expressed with an
ard
B gene (
swoo
_0276).
Together, these genes encode flavocytochrome
c
ArdAB, which is thus responsible for acrylate reduction in
S.
woodyi
cells.
ArdAB was highly specific for acrylate as substrate and reduced only methacrylate (at a 22-fold lower rate) among a series of other tested 2-enoates.
In line with these findings, acrylate and methacrylate induced
ard
A gene expression in
S.
woodyi
under anaerobic conditions, which was accompanied by the appearance of periplasmic acrylate reductase activity.
ArdAB-linked acrylate reduction supports dimethylsulfoniopropionate-dependent anaerobic respiration in
S.
woodyi
and, possibly, other marine bacteria.
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