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Glutathione disulfide and S-nitrosoglutathione detoxification by Mycobacteriumtuberculosis thioredoxin system
Authors:Rodgoun Attarian
Institution:Department of Medicine, Division of Infectious Diseases, University of British Columbia, Vancouver, British Columbia, Canada V5Z 3J5
Abstract:Mycobacterium tuberculosis resides within alveolar macrophages. These phagocytes produce reactive nitrogen and oxygen intermediates to combat the invading pathogens. The macrophage glutathione (GSH) pool reduces nitric oxide (NO) to S-nitrosoglutathione (GSNO). Both glutathione disulfide (GSSG) and GSNO possess mycobactericidal activities in vitro. In this study we demonstrate that M. tuberculosis thioredoxin system, comprises of thioredoxin reductase B2 and thioredoxin C reduces the oxidized form of the intracellular mycothiol (MSSM) and is able to efficiently reduce GSSG and GSNO in vitro. Our study suggests that the thioredoxin system provide a general reduction mechanism to cope with oxidative stress associated with the microbe’s metabolism as well as to detoxify xenobiotics produced by the host.
Keywords:DTNB  5  5&prime  -dithiobis-(2-nitrobenzoic acid)  GSH  glutathione  GS-mB  bimane derivative of GSH  GSSG  glutathione disulfide  GSNO  S-nitrosoglutathione  LMW  low molecular weight  mBBr  monobromobimane  MSH  mycothiol  MS-mB  bimane derivative of mycothiol  MSSM  oxidized mycothiol (mycothione)  NEM  n-ethylmaleimide  NO  nitric oxide  RNI  reactive nitrogen intermediates  ROI  reactive oxygen intermediates
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