Dissection of the Glycosylation in the Biosynthesis of the Heptadecaglycoside Antibiotic Saccharomicin A

J Org Chem. 2021 Aug 20;86(16):11117-11124. doi: 10.1021/acs.joc.0c03056. Epub 2021 Mar 16.

Abstract

Oligosaccharide natural products have diverse biological activities and represent a potentially important source for drug development. In this study, we focus on the glycosylation pathway in the biosynthesis of saccharomicin A (SA-A), an oligosaccharide antibiotic containing 17 sugar moieties. By extensive gene-knockout studies with comparative metabolic profile analysis, we established a complete pathway in assembling the heptadecasaccharide chain of SA-A, the longest saccharide chain found in natural products.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents*
  • Dissection
  • Glycosylation
  • Oligosaccharides*

Substances

  • Anti-Bacterial Agents
  • Oligosaccharides
  • saccharomicin A