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The mechanism of formate oxidation by metal-dependent formate dehydrogenases

dc.contributor.authorMota, Cristiano S.
dc.contributor.authorRivas, Maria G.
dc.contributor.authorBrondino, Carlos D.
dc.contributor.authorMoura, Isabel
dc.contributor.authorMoura, José J. G.
dc.contributor.authorGonzález, Pablo J.
dc.contributor.authorCerqueira, Nuno M. F. S. A.
dc.date.accessioned2013-01-30T10:06:13Z
dc.date.available2013-01-30T10:06:13Z
dc.date.issued2011
dc.descriptionJ Biol Inorg Chem (2011) 16:1255–1268 DOI 10.1007/s00775-011-0813-8por
dc.description.abstractMetal-dependent formate dehydrogenases (Fdh) from prokaryotic organisms are members of the dimethyl sulfoxide reductase family of mononuclear molybdenum-containing and tungsten-containing enzymes. Fdhs catalyze the oxidation of the formate anion to carbon dioxide in a redox reaction that involves the transfer of two electrons from the substrate to the active site. The active site in the oxidized state comprises a hexacoordinated molybdenum or tungsten ion in a distorted trigonal prismatic geometry. Using this structural model, we calculated the catalytic mechanism of Fdh through density functional theory tools. The simulated mechanism was correlated with the experimental kinetic properties of three different Fdhs isolated from three different Desulfovibrio species. Our studies indicate that the C–H bond break is an event involved in the rate-limiting step of the catalytic cycle. The role in catalysis of conserved amino acid residues involved in metal coordination and near the metal active site is discussed on the basis of experimental and theoretical results.por
dc.identifier.issn1432-1327
dc.identifier.urihttp://hdl.handle.net/10362/8611
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSpringerpor
dc.relation.ispartofseries8;
dc.relation.publisherversionhttp://link.springer.com/article/10.1007%2Fs00775-011-0813-8por
dc.subjectFormate dehydrogenasepor
dc.subjectReaction mechanismpor
dc.subjectMolybdenumpor
dc.subjectTungstenpor
dc.subjectDensity functional theorypor
dc.titleThe mechanism of formate oxidation by metal-dependent formate dehydrogenasespor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage1268por
oaire.citation.startPage1255por
oaire.citation.titleJournal of Biological Inorganic Chemistrypor
oaire.citation.volume16por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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