Hatfield_1991_Anal.Biochem_194_25

Reference

Title : Synthesis of methyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside and its use as a substrate to assess feruloyl esterase activity - Hatfield_1991_Anal.Biochem_194_25
Author(s) : Hatfield RD , Helm RF , Ralph J
Ref : Analytical Biochemistry , 194 :25 , 1991
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.

PubMedSearch : Hatfield_1991_Anal.Biochem_194_25
PubMedID: 1867381

Related information

Substrate Ara-FA

Citations formats

Hatfield RD, Helm RF, Ralph J (1991)
Synthesis of methyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside and its use as a substrate to assess feruloyl esterase activity
Analytical Biochemistry 194 :25

Hatfield RD, Helm RF, Ralph J (1991)
Analytical Biochemistry 194 :25