Synthesis of methyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside and its use as a substrate to assess feruloyl esterase activity

Anal Biochem. 1991 Apr;194(1):25-33. doi: 10.1016/0003-2697(91)90146-k.

Abstract

A synthetic scheme was developed for the production of methyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside (FA-Ara) in gram quantities. This molecule accurately models the chemical attachment of ferulic acid to polysaccharides found in cell walls of plants in the Gramineae family. It is therefore a realistic substrate that can be used to monitor feruloyl esterase activity. Ultraviolet spectral analysis indicated that FA-Ara has an absorption maximum distinct from the hydrolytic product, ferulic acid (FA), over a wide range of solution pH values. The log molar extinction coefficient ranges from 4.16 to 4.36 for FA-Ara and 4.16 to 4.33 for FA depending upon the pH of the buffered solution. Consequently a convenient spectrophotometric assay can be utilized to monitor esterase activity. Three different methods were developed for using this model substrate to assess esterase activity, including thin-layer chromatography, a spectrophotometric assay, and the use of high-performance liquid chromatography.

MeSH terms

  • Arabinose / analogs & derivatives*
  • Arabinose / chemical synthesis
  • Carboxylic Ester Hydrolases / metabolism*
  • Chromatography, High Pressure Liquid
  • Chromatography, Thin Layer
  • Coumaric Acids / chemical synthesis*
  • Hydrogen-Ion Concentration
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Spectrophotometry
  • Substrate Specificity

Substances

  • Coumaric Acids
  • methyl 5-O-feruloylarabinofuranoside
  • Arabinose
  • Carboxylic Ester Hydrolases
  • feruloyl esterase