Heterogeneous structure of O-antigenic part of lipopolysaccharide of Salmonella telaviv (Serogroup O:28) containing 3-acetamido-3,6-dideoxy-D-glucopyranose
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  • 作者:J. Kumirska (1) kumirska@chem.univ.gda.pl
    H. Dziadziuszko (2) halim@gumed.edu.pl
    M. Czerwicka (1) margo@chem.univ.gda.pl
    E. A. Lubecka (1) emilial@chem.univ.gda.pl
    D. Kunikowska (2) dankun@gumed.edu.pl
    E. M. Siedlecka (1) ewas@chem.univ.gda.pl
    P. Stepnowski (1) sox@chem.univ.gda.pl
  • 关键词:Salmonella Telaviv – ; O ; antigen – ; structural analysis – ; 3 ; acetamido ; 3 ; 6 ; dideoxy ; D ; glucose
  • 刊名:Biochemistry (Moscow)
  • 出版年:2011
  • 出版时间:July 2011
  • 年:2011
  • 卷:76
  • 期:7
  • 页码:780-790
  • 全文大小:366.9 KB
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  • 作者单位:1. Department of Chemistry, University of Gdansk, Sobieskiego 18, 80-952 Gdansk, Poland2. Department of Molecular Microbiology and Serology, National Salmonella Centre, Medical University of Gdansk, Do Studzienki 38, 80-227 Gdansk, Poland
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Biochemistry
    Bioorganic Chemistry
    Microbiology
    Biomedicine
    Russian Library of Science
  • 出版者:MAIK Nauka/Interperiodica distributed exclusively by Springer Science+Business Media LLC.
  • ISSN:1608-3040
文摘
The O-polysaccharide of Salmonella Telaviv was obtained by mild acid degradation of the lipopolysaccharide and studied by chemical methods (sugar and methylation analyses, Smith degradation, de-O-acetylation) and NMR spectroscopy. The structure of the O-polysaccharide was established. The repeating units that are proximal to the lipopolysaccharide core region mostly have a digalactose side chain and lack glucose, whereas those at the other end of the chain mostly do bear glucose but are devoid of the disaccharide side chain. This is the first structure established for the O-polysaccharide of a Salmonella serogroup O:28 (formerly M) strain characterized by subfactors O281 and O282. Knowledge of this structure and the structure of the O-polysaccharide of Salmonella Dakar (O281, O283) established earlier is crucial for determination of the exact structures associated with subfactors O281, O282, and O283 and elucidation of the genetic basis of the close relationship between Escherichia coli O71 and S. enterica O:28 O-antigens.
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