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

被引:124
作者
Seth, Divya [1 ,2 ,3 ]
Hausladen, Alfred [1 ,2 ,3 ]
Wang, Ya-Juan [4 ]
Stamler, Jonathan S. [1 ,2 ,3 ]
机构
[1] Case Western Reserve Univ, Sch Med, Inst Transformat Mol Med, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Med, Cleveland, OH 44106 USA
[3] Univ Hosp, Case Med Ctr, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Ctr Prote & Bioinformat, Cleveland, OH 44106 USA
关键词
ESCHERICHIA-COLI; NITRIC-OXIDE; NITROSATIVE STRESS; REDUCTASE; FNR; NITRATE; FLAVOHEMOGLOBIN; ACTIVATION; MECHANISM; CATALYSIS;
D O I
10.1126/science.1215643
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:470 / 473
页数:4
相关论文
共 26 条
[1]   Protein denitrosylation: enzymatic mechanisms and cellular functions [J].
Benhar, Moran ;
Forrester, Michael T. ;
Stamler, Jonathan S. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (10) :721-732
[2]   Dinitrosyliron complexes and the mechanism(s) of cellular protein nitrosothiol formation from nitric oxide [J].
Bosworth, Charles A. ;
Toledo, Jose C., Jr. ;
Zmijewski, Jaroslaw W. ;
Li, Qian ;
Lancaster, Jack R., Jr. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (12) :4671-4676
[3]  
CALMELS S, 1988, J GEN MICROBIOL, V134, P221
[4]   Nitric oxide formation by Escherichia coli -: Dependence on nitrite reductase, the NO-sensing regulator FNR, and flavohemoglobin Hmp [J].
Corker, H ;
Poole, RK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (34) :31584-31592
[5]   NO sensing by FNR:: regulation of the Escherichia coli NO-detoxifying flavohaemoglobin, Hmp [J].
Cruz-Ramos, H ;
Crack, J ;
Wu, GG ;
Hughes, MN ;
Scott, C ;
Thomson, AJ ;
Green, J ;
Poole, RK .
EMBO JOURNAL, 2002, 21 (13) :3235-3244
[6]   The NsrR regulon of Escherichia coli K-12 includes genes encoding the hybrid cluster protein and the periplasmic, respiratory nitrite reductase [J].
Filenko, Nina ;
Spiro, Stephen ;
Browning, Douglas F. ;
Squire, Derrick ;
Overton, Tim W. ;
Cole, Jeff ;
Constantinidou, Chrystala .
JOURNAL OF BACTERIOLOGY, 2007, 189 (12) :4410-4417
[7]   Protein S-nitrosylation in health and disease: a current perspective [J].
Foster, Matthew W. ;
Hess, Douglas T. ;
Stamler, Jonathan S. .
TRENDS IN MOLECULAR MEDICINE, 2009, 15 (09) :391-404
[8]   A Genetic Analysis of Nitrosative Stress [J].
Foster, Matthew W. ;
Liu, Limin ;
Zeng, Ming ;
Hess, Douglas T. ;
Stamler, Jonathan S. .
BIOCHEMISTRY, 2009, 48 (04) :792-799
[9]   Regulation of the nitric oxide reduction operon (norRVW) in Escherichia coli -: Role of norR and σ54 in the nitric oxide stress response [J].
Gardner, AM ;
Gessner, CR ;
Gardner, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (12) :10081-10086
[10]   A novel type of nitric-oxide reductase -: Escherichia coli flavorubredoxin [J].
Gomes, CM ;
Giuffrè, A ;
Forte, E ;
Vicente, JB ;
Saraiva, LM ;
Brunori, M ;
Teixeira, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (28) :25273-25276