Direct electrochemically driven catalysis of bovine milk xanthine oxidase


Autoria(s): Bernhardt, P. V.; Honeychurch, M. J.; McEwan, A. G.
Data(s)

01/01/2006

Resumo

The complex molybdoenzyme xanthine oxidase (XO) catalyses the oxidation of xanthine to uric acid. Here we report the first direct (unmediated) catalytic electrochemistry of the enzyme in the presence of xanthine. The only non-turnover response (without substrate present) is a sharp two-electron wave from the FAD cofactor at -242 mV vs. NHE (pH 8.0). Upon addition of xanthine to the electrochemical cell a pronounced electrocatalytic anodic current appears at ca. +300 mV vs. NHE, but the FAD peak remains. This is unusual as the onset of catalysis should occur at the potential of the FAD cofactor (the site at which oxygen or NAD+ binds to the enzyme in solution). The observed electrochemical catalysis is prevented by the addition of known XO inhibitors allopurinol or cyanide. (c) 2005 Elsevier B.V. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:79862

Idioma(s)

eng

Publicador

Elsevier Science Inc

Palavras-Chave #Xanthine Oxidase #Enzyme #Catalysis #Voltammetry #Electrochemistry #Rhodobacter-capsulatus #Uric-acid #Dehydrogenase #Molybdenum #Electrodes #Inactivation #Mechanism #Oxidation #Enzymes #C1 #250107 Electrochemistry #780103 Chemical sciences
Tipo

Journal Article