alpha-Mannosidase-catalyzed synthesis of a (1-->2)-alpha-D-rhamnodisaccharide derivative

Carbohydr Res. 2004 May 17;339(7):1389-93. doi: 10.1016/j.carres.2004.01.015.

Abstract

Enzymatic transglycosylation using p-nitrophenyl alpha-D-rhamnopyranoside as the glycosyl donor and 6equiv of ethyl 1-thio-alpha-D-rhamnopyranoside as the glycosyl acceptor yielded a D-rhamnooligosaccharide derivative. The reaction was catalyzed by jack bean alpha-mannosidase in a 1:1 (v/v) mixture of 0.1 M sodium citrate buffer (pH4.5)-MeCN at 25 degrees C. The enzyme exhibited high catalytic activity for the reaction, to afford in 32.1% isolated yield (based on donor substrate) ethyl alpha-D-rhamnopyranosyl-(1-->2)-1-thio-alpha-D-rhamnopyranoside, which is a derivative of the common oligosaccharide unit of the antigenic lipopolysaccharides from Pseudomonas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Disaccharides / biosynthesis*
  • Disaccharides / chemistry*
  • Glycosylation
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • alpha-Mannosidase / chemistry*
  • alpha-Mannosidase / metabolism

Substances

  • Disaccharides
  • ethyl rhamnopyranosyl-(1-2)-1-thiorhamnopyranoside
  • alpha-Mannosidase