Regioselective syntheses of trehalose-containing trisaccharides using various glycohydrolases

Carbohydr Res. 1990 Jun 1;199(2):227-34. doi: 10.1016/0008-6215(90)84264-u.

Abstract

Two methods were investigated for the enzymic preparation of trehalose-containing trisaccharides. In the first, a solution of saccharides is circulated through an immobilized-glycosidase column and an activated-carbon column connected in series. In the second, two enzymes having different substrate specificities are sequentially used for condensation and subsequent specific hydrolysis. Thus, 3-O-beta-D-, 4-O-beta-D-, and 6-O-beta-D-galactopyranosyl-alpha,alpha-trehalose; 4-O-alpha-D- and 6-O-alpha-D-glucopyranosyl-alpha,alpha-trehalose; and 4-O-beta-D- and 6-O-beta-D-glucopyranosyl-alpha,alpha-trehalose were synthesized stereo- and regio-selectively.

MeSH terms

  • Antigens, Bacterial / chemical synthesis
  • Antigens, Surface / chemical synthesis
  • Carbohydrate Sequence
  • Disaccharides*
  • Glycoside Hydrolases
  • Molecular Sequence Data
  • Mycobacterium / immunology
  • Trehalose* / analogs & derivatives
  • Trisaccharides / chemical synthesis*

Substances

  • Antigens, Bacterial
  • Antigens, Surface
  • Disaccharides
  • Trisaccharides
  • Trehalose
  • Glycoside Hydrolases