New chromogenic substrates for feruloyl esterases

Org Biomol Chem. 2008 Apr 7;6(7):1208-14. doi: 10.1039/b717742a. Epub 2008 Feb 29.

Abstract

Indolyl and nitrophenyl 5-O-hydroxycinnamoyl-alpha-L-arabinofuranosides were prepared by chemo-enzymatic syntheses. These probes were designed as substrates to be used in assays of feruloyl esterase activity (EC 3.1.1.77). Color development in the assays only occurs when feruloyl esterase activity releases an intermediate chromogenic arabinoside that is a suitable substrate for alpha-L-arabinofuranosidase (EC 3.2.1.55), which in turn releases the free chromogenic group. The usefulness of these compounds was evaluated in both qualitative solid media-based assays and quantitative liquid assays that can be performed in microtiter plates using feruloyl esterases and arabinofuranosidases from various origins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carboxylic Ester Hydrolases / analysis*
  • Carboxylic Ester Hydrolases / chemistry*
  • Chromogenic Compounds / chemical synthesis
  • Chromogenic Compounds / chemistry*
  • Molecular Probes / chemical synthesis
  • Molecular Probes / chemistry
  • Molecular Structure
  • Nitrophenols / chemistry

Substances

  • Chromogenic Compounds
  • Molecular Probes
  • Nitrophenols
  • 2-chloro-4-nitrophenyl acetate
  • Carboxylic Ester Hydrolases
  • feruloyl esterase