Characterization of a new aryl-alcohol oxidase secreted by the phytopathogenic fungus Ustilago maydis

Appl Microbiol Biotechnol. 2016 Jan;100(2):697-706. doi: 10.1007/s00253-015-7021-3. Epub 2015 Oct 9.

Abstract

The discovery of novel fungal lignocellulolytic enzymes is essential to improve the breakdown of plant biomass for the production of second-generation biofuels or biobased materials in green biorefineries. We previously reported that Ustilago maydis grown on maize secreted a diverse set of lignocellulose-acting enzymes including hemicellulases and putative oxidoreductases. One of the most abundant proteins of the secretome was a putative glucose-methanol-choline (GMC) oxidoreductase. The phylogenetic prediction of its function was hampered by the few characterized members within its clade. Therefore, we cloned the gene and produced the recombinant protein to high yield in Pichia pastoris. Functional screening using a library of substrates revealed that this enzyme was able to oxidize several aromatic alcohols. Of the tested aryl-alcohols, the highest oxidation rate was obtained with 4-anisyl alcohol. Oxygen, 1,4-benzoquinone, and 2,6-dichloroindophenol can serve as electron acceptors. This GMC oxidoreductase displays the characteristics of an aryl-alcohol oxidase (E.C.1.1.3.7), which is suggested to act on the lignin fraction in biomass.

Keywords: AA3; Aryl-alcohol oxidase; Biorefinery; CAZy; Lignin; Ustilago maydis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2,6-Dichloroindophenol / metabolism
  • Alcohol Oxidoreductases / genetics*
  • Alcohol Oxidoreductases / metabolism*
  • Benzoquinones / metabolism
  • Biomass
  • Electron Transport
  • Lignin / metabolism*
  • Oxygen / metabolism
  • Phylogeny
  • Pichia / genetics
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Ustilago / enzymology*
  • Ustilago / metabolism

Substances

  • Benzoquinones
  • Recombinant Proteins
  • lignocellulose
  • Lignin
  • 2,6-Dichloroindophenol
  • Alcohol Oxidoreductases
  • aryl-alcohol oxidase
  • Oxygen