Nitrite reduction by xanthine oxidase family enzymes: a new class of nitrite re...

• Author(s): Maia, Luisa B. ; Moura, José J. G.
• Date: 2011
• Persistent ID: http://hdl.handle.net/10362/8621
• Origin: Repositório Institucional da UNL
• Subject(s): Nitrite reduction; Nitric oxide formation; Molybdenum; Xanthine oxidase; Aldehyde oxidoreductase
• Document Type: Article
• Language: English

Description

J Biol Inorg Chem (2011) 16:443–460 DOI 10.1007/s00775-010-0741-z Mammalian xanthine oxidase (XO) and Desulfovibrio gigas aldehyde oxidoreductase (AOR) are members of the XO family of mononuclear molybdoenzymes that catalyse the oxidative hydroxylation of a wide range of aldehydes and heterocyclic compounds. Much less known is the XO ability to catalyse the nitrite reduction to nitric oxide radical (NO). To assess the competence of other XO family enzymes to catalyse the nitrite reduction and to shed some light onto the molecular mechanism of this reaction, we characterised the anaerobic XO- and AORcatalysed nitrite reduction. The identification of NO as the reaction product was done with a NO-selective electrode and by electron paramagnetic resonance (EPR) spectroscopy. The steady-state kinetic characterisation corroborated the XO-catalysed nitrite reduction and demonstrated, for the first time, that the prokaryotic AOR does catalyse the nitrite reduction to NO, in the presence of any electron donor to the enzyme, substrate (aldehyde) or not (dithionite). Nitrite binding and reduction was shown by EPR spectroscopy to occur on a reduced molybdenum centre. A molecular mechanism of AOR- and XO-catalysed nitrite reduction is discussed, in which the higher oxidation states of molybdenum seem to be involved in oxygen-atom insertion, whereas the lower oxidation states would favour oxygenatom abstraction. Our results define a new catalytic performance for AOR—the nitrite reduction—and propose a new class of molybdenum-containing nitrite reductases. Keywords Nitrite reduction Nitric oxide formation Molybdenum Xanthine oxidase Aldehyde oxidoreductase Abbreviations AOR Aldehyde oxidoreductase DMSOR Dimethylsulfoxide reductase EPR Electron paramagnetic resonance Fe/S Iron–sulfur centre Fe/S–NO Dinitrosyl–iron–sulfur complex (MGD)2–Fe Ferrous complex of di(N-methyl-Dglucamine dithiocarbamate)(MGD)2–Fe–NO Mononitrosyl–iron complex Mo-enzymes Pterin–molybdenum-containing enzymes NaR Nitrate reductases NO Nitric oxide radical SO Sulfite oxidase XO Xanthine oxidase Introduction Molybdenum is present in a wide variety of enzymes, in both prokaryotes and eukaryotes, where it performs catalytic