The mercaptopyruvate sulfurtransferase of Trichomonas vaginalis links cysteine catabolism to the production of thioredoxin persulfide

Westrop, G. D., Georg, I. and Coombs, G. H. (2009) The mercaptopyruvate sulfurtransferase of Trichomonas vaginalis links cysteine catabolism to the production of thioredoxin persulfide. Journal of Biological Chemistry, 284(48), pp. 33485-33494. (doi: 10.1074/jbc.M109.054320)

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<i>Trichomonas vaginalis</i> is a protozoan parasite of humans that is able to synthesize cysteine de novo using cysteine synthase but does not produce glutathione. In this study, high pressure liquid chromatography analysis confirmed that cysteine is the major intracellular redox buffer by showing that <i>T. vaginalis</i> contains high levels of cysteine (∼600 μM) comprising more than 70% of the total thiols detected. To investigate possible mechanisms for the regulation of cysteine levels in <i>T. vaginalis</i>, we have characterized enzymes of the mercaptopyruvate pathway. This consists of an aspartate aminotransferase (TvAspAT1), which transaminates cysteine to form 3-mercaptopyruvate (3-MP), and mercaptopyruvate sulfurtransferase (TvMST), which transfers the sulfur of 3-MP to a nucleophilic acceptor, generating pyruvate. TvMST has high activity with 3-MP as a sulfur donor and can use several thiol compounds as sulfur acceptor substrates. Our analysis indicated that TvMST has a k<sub>cat</sub>/K<sub>m</sub> for reduced thioredoxin of 6.2 × 10<sup>7</sup> M<sup>−1</sup> s<sup>−1</sup>, more than 100-fold higher than that observed for β-mercaptoethanol and cysteine, suggesting that thioredoxin is a preferred substrate for TvMST. Thiol trapping and mass spectrometry provided direct evidence for the formation of thioredoxin persulfide as a product of this reaction. The thioredoxin persulfide could serve a biological function such as the transfer of the persulfide to a target protein or the sequestered release of sulfide for biosynthesis. Changes in MST activity of <i>T. vaginalis</i> in response to variation in the supply of exogenous cysteine are suggestive of a role for the mercaptopyruvate pathway in the removal of excess intracellular cysteine, redox homeostasis, and antioxidant defense.

Item Type:Articles
Glasgow Author(s) Enlighten ID:Coombs, Professor Graham
Authors: Westrop, G. D., Georg, I., and Coombs, G. H.
College/School:College of Medical Veterinary and Life Sciences > School of Life Sciences
Journal Name:Journal of Biological Chemistry
Journal Abbr.:J Biol Chem.
Publisher:American Society for Biochemistry and Molecular Biology
ISSN (Online):1083-351X
Published Online:17 September 2009
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Project CodeAward NoProject NamePrincipal InvestigatorFunder's NameFunder RefLead Dept
241292Molecular Genetic and Biochemical Analyses of ParasitesJeremy MottramMedical Research Council (MRC)G9722968:ID5536Infection Immunity and Inflammation Life Sciences