Acyl-acyl carrier protein specificity of UDP-GlcNAc acyltransferases from gram-negative bacteria: relationship to lipid A structure

J Bacteriol. 1991 Jun;173(11):3591-6. doi: 10.1128/jb.173.11.3591-3596.1991.

Abstract

Lipid A, the component of lipopolysaccharide that provides the membrane anchor of the core and O-antigen sugars, is known to contain characteristic R-3-hydroxy fatty acids bound to the 2,2' (N-linked) and 3,3' (O-linked) positions of the glucosamine disaccharide in different gram-negative bacteria. The studies reported here show that it is the acyl-acyl carrier protein specificities of the enzymes UDP-GlcNAc-O-acyltransferase and UDP-3-O-[(R)-3-hydroxyacyl]-GlcN-N-acyltransferase that determine the nature of these fatty acids.

MeSH terms

  • Acinetobacter / enzymology*
  • Acyl Carrier Protein / chemistry*
  • Acylation
  • Acyltransferases / chemistry*
  • Enterobacteriaceae
  • Lipid A / chemistry*
  • Pseudomonas aeruginosa / enzymology*
  • Rhodobacter sphaeroides / enzymology*

Substances

  • Acyl Carrier Protein
  • Lipid A
  • Acyltransferases
  • acyl-(acyl-carrier-protein)-UDP-N-acetylglucosamine acyltransferase