A spectrophotometric assay for the detection of fungal peroxygenases

Anal Biochem. 2012 Feb 1;421(1):327-9. doi: 10.1016/j.ab.2011.10.009. Epub 2011 Oct 8.

Abstract

Rapid and simple spectrophotometric methods are required for the unambiguous detection of recently discovered fungal peroxygenases in vivo and in vitro. This paper describes a peroxygenase-specific assay using 5-nitro-1,3-benzodioxole as substrate. The product, 4-nitrocatechol, produces a yellow color at pH 7, which can be followed over time at 425 nm (ε(425)=9,700 M(-1) cm(-1)), and a red color when adjusted to pH >12, which can be measured in form of an end-point determination at 514 nm (ε(514)=11,400 M(-1) cm(-1)). The assay is suitable for detecting peroxygenase activities in complex growth media and environmental samples as well as for high-throughput screenings.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catechols / metabolism
  • Dioxoles / metabolism
  • Fungi / enzymology*
  • High-Throughput Screening Assays / methods
  • Hydrogen-Ion Concentration
  • Mixed Function Oxygenases / analysis*
  • Mixed Function Oxygenases / metabolism
  • Spectrophotometry / methods*

Substances

  • Catechols
  • Dioxoles
  • Mixed Function Oxygenases
  • peroxygenase
  • 1,3-benzodioxole
  • 4-nitrocatechol