'Thermodynamic' mechanism of catalysis by haloperoxidases

FEBS Lett. 1996 Apr 1;383(3):259-63. doi: 10.1016/0014-5793(96)00209-8.

Abstract

A novel 'thermodynamic' mechanistic rationale of haloperoxidase catalysis is based on the following two assumptions: (i) the role of enzyme consists only in the rapid equilibration between the halogen-containing species originating from halide and hydrogen peroxide; (ii) the interaction between the enzyme and organic substrate is kinetically insignificant and halogenation occurs as a result of the electrophilic attack of the active brominating (Br3-, Br2 and HBrO) or chlorinating (HCIO) species at monochlorodimedon indicative of a higher chloride 'specificity' of chloroperoxidase from C. fumago.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Chloride Peroxidase / chemistry*
  • Chloride Peroxidase / metabolism*
  • Kinetics
  • Mitosporic Fungi / enzymology
  • Models, Theoretical
  • Peroxidases / chemistry*
  • Peroxidases / metabolism*
  • Substrate Specificity
  • Thermodynamics

Substances

  • Peroxidases
  • Chloride Peroxidase