Development of a method to measure laccase activity on methoxyphenolic food ingredients and isomers

Int J Biol Macromol. 2020 May 15:151:1099-1107. doi: 10.1016/j.ijbiomac.2019.10.152. Epub 2019 Nov 18.

Abstract

We studied the laccase-catalysed oxygenation of methoxyphenolic food ingredients, such as 2-methoxyphenol (guaiacol) and 2,6-dimethoxyphenol (syringol), isomers such as 3- and 4-methoxyphenol, and 2,3-, 3,4- and 3,5-dimethoxyphenol. These methoxyphenolic substrates generate unstable free radicals, which leads to the erroneous determination of steady state rates. The addition of small quantities of ascorbic acid as coupling reagent generates a lag period because it reduces free radicals to methoxyphenols. Measurement of the length of the lag period provides the reliable determination of true steady state rates. We describe the application of this chronometric method to the kinetic characterization of the oxidation of the above methoxyphenolic substrates by Trametes versicolor laccase.

Keywords: 2,6-Dimethoxyphenol; Chronometric method; Guaiacol; Laccase; Methoxyphenols; Trametes versicolor.

MeSH terms

  • Ascorbate Oxidase / chemistry
  • Enzyme Activation
  • Enzyme Assays / methods*
  • Food Ingredients / analysis*
  • Hydrogen-Ion Concentration
  • Isomerism
  • Kinetics
  • Laccase / chemistry*
  • Molecular Structure
  • Phenols / analysis*
  • Spectrum Analysis
  • Substrate Specificity

Substances

  • Food Ingredients
  • Phenols
  • Laccase
  • Ascorbate Oxidase