Structure and genetics of the O-antigen of Enterobacter cloacae G3054 containing di-N-acetylpseudaminic acid

Carbohydr Res. 2015 Apr 30:407:59-62. doi: 10.1016/j.carres.2015.01.015. Epub 2015 Jan 31.

Abstract

Mild acid degradation of the lipopolysaccharide of Enterobacter cloacae G3054 resulted in the cleavage of the O-polysaccharide at the linkage of residues of 5,7-diacetamido-3,5,7,9-tetradeoxy-L-glycero-L-manno-non-2-ulosonic acid (di-N-acetylpseudaminic acid, Pse5Ac7Ac) in the main chain. The resultant oligosaccharide and an alkali-treated lipopolysaccharide were studied by sugar analysis along with (1)H and (13)C NMR spectroscopy, and the following structure of the branched pentasaccharide O-unit of the O-polysaccharide was established: [structure: see text] The O-antigen gene cluster of E. cloacae G3054 between conserved genes galF and gnd was sequenced. Most genes necessary for the O-antigen synthesis were found in the cluster and their functions were tentatively assigned by comparison with sequences in the available databases.

Keywords: Bacterial polysaccharide structure; Enterobacter cloacae; O-antigen; O-antigen gene cluster; Pseudaminic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Sequence
  • Enterobacter cloacae / genetics*
  • Enterobacter cloacae / metabolism
  • Lipopolysaccharides / chemistry
  • Multigene Family
  • O Antigens / chemistry*
  • O Antigens / genetics*
  • O Antigens / isolation & purification
  • Proton Magnetic Resonance Spectroscopy
  • Sialic Acids / chemistry*

Substances

  • 5,7-diacetamido-3,5,7,9-tetradeoxynon-2-ulosonic acid
  • Lipopolysaccharides
  • O Antigens
  • Sialic Acids