General Tolerance of Galactosyltransferases toward UDP-galactosamine Expands Their Synthetic Capability

Angew Chem Int Ed Engl. 2021 Dec 13;60(51):26555-26560. doi: 10.1002/anie.202112574. Epub 2021 Nov 9.

Abstract

Accessing large numbers of structurally diverse glycans and derivatives is essential to functional glycomics. We showed a general tolerance of galactosyltransferases toward uridine-diphosphate-galactosamine (UDP-GalN), which is not a commonly used sugar nucleotide donor. The property was harnessed to develop a two-step chemoenzymatic strategy for facile synthesis of novel and divergent N-acetylgalactosamine (GalNAc)-glycosides and derivatives in preparative scales. The discovery and the application of the new property of existing glycosyltransferases expand their catalytic capabilities in generating novel carbohydrate linkages, thus prompting the synthesis of diverse glycans and glycoconjugates for biological studies.

Keywords: GalNAc-glycosides; UDP-galactosamine; galactosyltransferase; general tolerance.

Publication types

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

MeSH terms

  • Carbohydrate Conformation
  • Galactosyltransferases / metabolism*
  • Helicobacter pylori / enzymology
  • Neisseria meningitidis / enzymology
  • Uridine Diphosphate N-Acetylgalactosamine / analogs & derivatives*
  • Uridine Diphosphate N-Acetylgalactosamine / biosynthesis
  • Uridine Diphosphate N-Acetylgalactosamine / chemistry

Substances

  • uridine diphosphate galactosamine
  • Uridine Diphosphate N-Acetylgalactosamine
  • Galactosyltransferases