4.8 Article

Endogenous Protein S-Nitrosylation in E. coli: Regulation by OxyR

Journal

SCIENCE
Volume 336, Issue 6080, Pages 470-473

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1215643

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Funding

  1. NIH [R01-HL096673, R01-HL095463, R01-HL059130]
  2. Defense Advanced Research Projects Agency [N66001-10-C-2015]

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Endogenous S-nitrosylation of proteins, a principal mechanism of cellular signaling in eukaryotes, has not been observed in microbes. We report that protein S-nitrosylation is an obligate concomitant of anaerobic respiration on nitrate in Escherichia coli. Endogenous S-nitrosylation during anaerobic respiration is controlled by the transcription factor OxyR, previously thought to operate only under aerobic conditions. Deletion of OxyR resulted in large increases in protein S-nitrosylation, and S-nitrosylation of OxyR induced transcription from a regulon that is distinct from the regulon induced by OxyR oxidation. Furthermore, products unique to the anaerobic regulon protected against S-nitrosothiols, and anaerobic growth of E. coli lacking OxyR was impaired on nitrate. Thus, OxyR serves as a master regulator of S-nitrosylation, and alternative posttranslational modifications of OxyR control distinct transcriptional responses.

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