Crystallization and preliminary X-ray analysis of the flavoenzyme vanillyl-alcohol oxidase from Penicillium simplicissimum

Proteins. 1997 Apr;27(4):601-3. doi: 10.1002/(sici)1097-0134(199704)27:4<601::aid-prot12>3.0.co;2-o.

Abstract

Vanillyl-alcohol oxidase catalyses the oxidation of several 4-hydroxybenzyl alcohols by using 8-alpha-(N3-histidyl)-FAD as a covalently bound prosthetic group. Crystals of vanillyl-alcohol oxidase from Penicillium simplicissimum have been grown by using the vapor diffusion technique. The space group was found to be I, with cell dimensions a = b = 140.5 A, c = 132.9 A. Diffraction data have been recorded to 3.2 A resolution by using a laboratory source and to 2.5 A resolution on flash freezing the crystal at the ELETTRA Synchrotron X-ray diffraction beam line.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Oxidoreductases / chemistry*
  • Crystallography, X-Ray
  • Flavin-Adenine Dinucleotide / chemistry
  • Flavoproteins / chemistry*
  • Penicillium / enzymology*

Substances

  • Flavoproteins
  • Flavin-Adenine Dinucleotide
  • Alcohol Oxidoreductases
  • vanillyl-alcohol oxidase