Solvent as a probe of active site motion and chemistry during the hydrogen tunnelling reaction in morphinone reductase

Chemphyschem. 2008 Sep 15;9(13):1875-81. doi: 10.1002/cphc.200800303.

Abstract

The reductive half-reaction of morphinone reductase involves a hydride transfer from enzyme-bound beta-nicotinamide adenine dinucleotide (NADH) to a flavin mononucleotide (FMN). We have previously demonstrated that this step proceeds via a quantum mechanical tunnelling mechanism. Herein, we probe the effect of the solvent on the active site chemistry. The pK(a) of the reduced FMN N1 is 7.4+/-0.7, based on the pH-dependence of the FMN midpoint potential. We rule out that protonation of the reduced FMN N1 is coupled to the preceding H-transfer as both the rate and temperature-dependence of the reaction are insensitive to changes in solution pH above and below this pK(a). Further, the solvent kinetic isotope effect is approximately 1.0 and both the 1 degrees and 2 degrees KIEs are insensitive to solution pH. The effect of the solvent's dielectric constant is investigated and the rate of H-transfer is found to be unaffected by changes in the dielectric constant between approximately 60 and 80. We suggest that, while there is crystallographic evidence for some water in the active site, the putative promoting motion involved in the H-tunnelling reaction is insensitive to such changes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / metabolism*
  • Binding Sites
  • Electrons
  • Flavin Mononucleotide / chemistry
  • Flavin Mononucleotide / metabolism
  • Hydrogen / chemistry*
  • Hydrogen-Ion Concentration
  • Isotopes
  • Kinetics
  • Models, Molecular
  • Molecular Structure
  • Oxidation-Reduction
  • Oxidoreductases / chemistry*
  • Oxidoreductases / metabolism*
  • Potentiometry
  • Solvents / chemistry*

Substances

  • Bacterial Proteins
  • Isotopes
  • Solvents
  • Flavin Mononucleotide
  • Hydrogen
  • Oxidoreductases
  • morphinone reductase