Publication | Open Access
Cysteine Oxidation Reactions Catalyzed by a Mononuclear Non-heme Iron Enzyme (OvoA) in Ovothiol Biosynthesis
52
Citations
31
References
2014
Year
BiosynthesisAldo-keto ReductaseBiochemistryMedicineBiocatalysisNatural SciencesEnzyme CatalysisOvothiol BiosynthesisMolecular BiologyHeme DegradationCatalysisPharmacologyDifferent Regio-selectivityRedox BiologyCysteine Sulfinic AcidOxidative Stress
OvoA in ovothiol biosynthesis is a mononuclear non-heme iron enzyme catalyzing the oxidative coupling between histidine and cysteine. It can also catalyze the oxidative coupling between hercynine and cysteine, yet with a different regio-selectivity. Due to the potential application of this reaction for industrial ergothioneine production, in this study, we systematically characterized OvoA by a combination of three different assays. Our studies revealed that OvoA can also catalyze the oxidation of cysteine to either cysteine sulfinic acid or cystine. Remarkably, these OvoA-catalyzed reactions can be systematically modulated by a slight modification of one of its substrates, histidine.
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