| Literature DB >> 29864581 |
Olesya I Naumenko1, Jingjie Song2, Sof'ya N Senchenkova3, Xiaohan Jiang2, Andrei V Perepelov4, Alexander S Shashkov3, Yuriy A Knirel3.
Abstract
Mild acid hydrolysis of the lipopolysaccharide of Escherichia coli O57 afforded an O-polysaccharide, which was isolated by gel permeation chromatography (GPC) and studied by sugar analysis, Smith degradation and solvolysis with trifluoroacetic acid, along with 2D 1H and 13C NMR spectroscopy. The O-polysaccharide was found to contain d-Glc, d-Gal, d-GalA, d-GlcNAc, and l-FucNAc, as well as O-acetyl groups. Smith degradation of the O-deacetylated polysaccharide destroyed side-branch β-Glсp and α-GalpA to give a modified linear polysaccharide. Solvolysis cleaved selectively the linkage of α-l-FucpNAc to give a pentasaccharide corresponding to the O-polysaccharide repeat. A comparison of the NMR spectra of the initial and O-deacetylated polysaccharides showed that α-GalpA is non-stoichiometrically O-acetylated at position either 2 (∼30%) or 3 (∼40%). The following structure of the O-polysaccharide was established, which is unique among known bacterial polysaccharide structures.Entities:
Keywords: Bacterial polysaccharide structure; CF(3)CO(2)H solvolysis; Escherichia coli; O-antigen; O-polysaccharide
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Year: 2018 PMID: 29864581 DOI: 10.1016/j.carres.2018.05.006
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104