Mechanism of hydroxylation of biphenyl by Cunninghamella echinulata

Biochem J. 1981 Apr 15;196(1):369-71. doi: 10.1042/bj1960369.

Abstract

The hydroxylation of [U-2H]biphenyl and [2,2',3,3',5,5',6,6'-2H]biphenyl by Cunninghamella echinulata A.T.C.C. 9244 has been studied. G.l.c.-mass-spectrometry analyses indicate the lack of an isotope effect during the hydroxylation of the perdeuterated substrate. Both g.l.c.-mass spectrometry and 1H n.m.r. were used to definitively demonstrate the presence of a 1,2-hydride-shift during the microbiological hydroxylation of [2,2',3,3',5,5',6,6'-2H]biphenyl.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biphenyl Compounds / metabolism*
  • Fungicides, Industrial / metabolism*
  • Gas Chromatography-Mass Spectrometry
  • Hydroxylation
  • Magnetic Resonance Spectroscopy
  • Mucorales / metabolism*

Substances

  • Biphenyl Compounds
  • Fungicides, Industrial
  • diphenyl