Enzymatic transglycosylation for glycoconjugate synthesis

Curr Opin Chem Biol. 2009 Dec;13(5-6):592-600. doi: 10.1016/j.cbpa.2009.08.014. Epub 2009 Sep 18.

Abstract

Remarkable advances have been made in recent years in exploiting the transglycosylation activity of glycosidases and glycosynthase mutants for oligosaccharide and glycoconjugate synthesis. New glycosynthases were generated from retaining glycosidases, inverting glycosidases, and those that proceed in a mechanism of substrate-assisted catalysis. Directed evolution coupled with elegant screening methods has led to the discovery of an expanding number of glycosynthase mutants that show improved catalytic activity and/or altered substrate specificity. In particular, enzymatic transglycosylation strategy has been recently extended to the synthesis of complex glycoconjugates, including glycosphingolipids, N-glycoproteins, and other glycosylated natural products.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Biocatalysis
  • Biological Products / biosynthesis
  • Biological Products / metabolism
  • Enzymes / metabolism*
  • Glycoconjugates / biosynthesis*
  • Glycoconjugates / metabolism
  • Glycoside Hydrolases / metabolism
  • Glycosides / metabolism
  • Glycosylation
  • Humans

Substances

  • Biological Products
  • Enzymes
  • Glycoconjugates
  • Glycosides
  • Glycoside Hydrolases
  • endoglycoceramidase