Inner-Sphere Mechanism for Molecular Oxygen Reduction Catalyzed by Copper Amine Oxidases.
June 29th, 2008 | by admin |Inner-Sphere Mechanism for Molecular Oxygen Reduction Catalyzed by Copper Amine Oxidases.
Copper and topaquinone (TPQ) containing amine oxidases utilize O 2 for the metabolism of biogenic amines while concomitantly generating H 2O 2 for use by the cell. The mechanism of O 2 reduction has been the subject of long-standing debate due to the obscuring influence of a proton-coupled electron transfer between the tyrosine-derived TPQ and copper, a rapidly established equilibrium precluding assignment of the enzyme in its reactive form. Here, we show that substrate-reduced pea seedling amine oxidase (PSAO) exists predominantly in the Cu (I), TPQ semiquinone state. A new mechanistic proposal for O 2 reduction is advanced on the basis of thermodynamic considerations together with kinetic studies (at varying pH, temperature, and viscosity), the identification of steady-state intermediates, and the analysis of competitive oxygen kinetic isotope effects, (18)O KIEs, [ k cat/ K M( (16,16)O 2)]/[ k cat/ K M( (16,18)O 2)]. The (18)O KIE = 1.0136 +/- 0.0013 at pH 7.2 is independent of temperature from 5 degrees C to 47 degrees C and insignificantly changed to 1.0122 +/- 0.0020 upon raising the pH to 9, thus indicating the absence of kinetic complexity. Using density functional methods, the effect is found to be precisely in the range expected for reversible O 2 binding to Cu (I) to afford a superoxide, [Cu (II)(eta (1)-O 2) (-I)] (+), intermediate. Electron transfer from the TPQ semiquinone follows in the first irreversible step to form a peroxide, Cu (II)(eta (1)-O 2) (-II), intermediate driving the reduction of O 2. The similar (18)O KIEs reported for copper amine oxidases from other sources raise the possibility that all enzymes react by related inner-sphere mechanisms although additional experiments are needed to test this proposal.
Mukherjee A, Smirnov VV, Lanci MP, Brown DE, Shepard EM, Dooley DM, Roth JP.
Department of Chemistry, Johns Hopkins University, 3400 North Charles St., Baltimore, Maryland 21218 and Department of Chemistry and Biochemistry, Montana State University, Bozeman, Montana 59717 jproth@jhu.edu.