Extracellular Oxidase from the Neonothopanus nambi Fungus as a Promising Enzyme for Analytical Applications

Protein J. 2021 Oct;40(5):731-740. doi: 10.1007/s10930-021-10010-z. Epub 2021 Jun 18.

Abstract

The extracellular enzyme with oxidase function was extracted from the Neonothopanus nambi luminescent fungus by using mild processing of mycelium with β-glucosidase and then isolated by gel-filtration chromatography. The extracted enzyme is found to be a FAD-containing protein, catalyzing phenol co-oxidation with 4-aminoantipyrine without addition of H2O2, which distinguishes it from peroxidases. This fact allowed us to assume that this enzyme may be a mixed-function oxidase. According to gel-filtration chromatography and SDS-PAGE, the oxidase has molecular weight of 60 kDa. The enzyme exhibits maximum activity at 55-70 °C and pH 5.0. Kinetic parameters Km and Vmax of the oxidase for phenol were 0.21 mM and 0.40 µM min-1. We suggest that the extracted enzyme can be useful to develop a simplified biosensor for colorimetric detection of phenol in aqueous media, which does not require using hydrogen peroxide.

Keywords: Extracellular oxidase; Flavoprotein; Fungi; Phenol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agaricales / enzymology*
  • Ampyrone / chemistry*
  • Catalysis
  • Fungal Proteins / chemistry*
  • Fungal Proteins / isolation & purification
  • Hydrogen Peroxide / chemistry*
  • Oxidoreductases / chemistry*
  • Oxidoreductases / isolation & purification

Substances

  • Fungal Proteins
  • Ampyrone
  • Hydrogen Peroxide
  • Oxidoreductases

Supplementary concepts

  • Neonothopanus nambi