Structural characterization of a novel diglycosyl diacylglyceride glycolipid from Rhizobium trifolii ANU843

Carbohydr Res. 1992 Sep 2:233:151-9. doi: 10.1016/s0008-6215(00)90927-3.

Abstract

A novel glycolipid was isolated by chloroform-methanol extraction of Rhizobium trifolii ANU843 cells. Compositional analysis, methylation studies, 1H NMR and spectroscopies led to the identification of a diglycosyl diacylglyceride: 1,2-di-O-acyl-3-O-[alpha-D-glucopyranosyl-(1----3)-O-alpha-D- mannopyranosyl]glycerol. Iso-hexadecanoic and anteiso-heptadecanoic acids were the predominant fatty acids esterifying the glyceryl moiety, but a microheterogeneity in fatty acid composition was found, resulting in at least five distinct molecular species of the glycolipid. Although widespread in plants, animals and Gram-positive bacteria, glycosyl glycerides have been seldom reported in Gram-negative bacteria and this work is the first evidence of their occurrence in the bacterial family Rhizobiaceae.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carbohydrate Sequence
  • Diglycerides / chemistry*
  • Methylation
  • Molecular Sequence Data
  • Rhizobium / chemistry*
  • Spectrum Analysis

Substances

  • Diglycerides