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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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