Abstract
S-form lipopolysaccharide was isolated by phenol/water extraction from a strain of Acinetobacter calcoaceticus (DNA group 1). The structure of the O-antigenic polysaccharide was determined by compositional analysis and NMR spectroscopy of the de-O-acylated lipopolysaccharide. The isolated polysaccharide obtained after hydrolysis of lipopolysaccharide in 0.01 M trifluoroacetic acid has the following structure: D(R)-Pyr(→4,6))→2)-β-D-Galp-(1→3)-β-D-GlcpNAc-(1→4)-β-D-GlcpA-(1→3)-β -D-Galp-Nac-(1→(Ac→3) in which Pyr is pyruvate. The O-acetyl substitution of D-Gal was non-stoichiometric. The O-antigen was specifically recognised in western blots by polyclonal rabbit antisera.
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Vinogradov, E. V., Pantophlet, R., Haseley, S. R., Brade, L., Holst, O., & Brade, H. (1997). Structural and serological characterisation of the O-specific polysaccharide from lipopolysaccharide of Acinetobacter calcoaceticus strain 7 (DNA group I). European Journal of Biochemistry, 243(1–2), 167–173. https://doi.org/10.1111/j.1432-1033.1997.0167a.x
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