Structure of the active site of sulfite oxidase. X-ray absorption spectroscopy of the Mo(IV), Mo(V), and Mo(VI) oxidation states

Biochemistry. 1989 Jun 13;28(12):5075-80. doi: 10.1021/bi00438a026.

Abstract

The active site of sulfite oxidase has been investigated by X-ray absorption spectroscopy at the molybdenum K-edge at 4 K. We have investigated all three accessible molybdenum oxidation states, Mo(IV), Mo(V), and Mo(VI), allowing comparison with the Mo(V) electron paramagnetic resonance data for the first time. Quantitative analysis of the extended X-ray absorption fine structure indicates that the Mo(VI) oxidation state possesses two terminal oxo (Mo = O) and approximately three thiolate-like (Mo-S-) ligands and is unaffected by changes in pH and chloride concentration. The Mo(IV) and Mo(V) oxidation states, however, each have a single oxo ligand plus one Mo-O- (or Mo-N less than) bond, most probably Mo--OH, and two to three thiolate-like ligands. Both reduced forms appear to gain a single chloride ligand under conditions of low pH and high chloride concentration.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Binding Sites
  • Chickens
  • Electron Spin Resonance Spectroscopy
  • Energy Transfer
  • Hydrogen-Ion Concentration
  • Liver / enzymology
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Molybdenum / analysis*
  • Molybdenum / pharmacology
  • Oxidation-Reduction
  • Oxidoreductases / analysis*
  • Oxidoreductases Acting on Sulfur Group Donors / analysis*

Substances

  • Molybdenum
  • Oxidoreductases
  • Oxidoreductases Acting on Sulfur Group Donors