Structural studies of the O-antigenic polysaccharides from the enteroaggregative Escherichia coli strain 87/D2 and international type strains from E. coli O128
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作者:
Ali, Tara
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Stockholm Univ, Dept Organ Chem, Arrhenius Lab, S-10691 Stockholm, Sweden
Karolinska Univ Hosp, Karolinska Inst, Dept Lab Med, Div Clin Microbiol, S-14186 Huddinge, SwedenStockholm Univ, Dept Organ Chem, Arrhenius Lab, S-10691 Stockholm, Sweden
Ali, Tara
[1
,2
]
Weintraub, Andrej
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Karolinska Univ Hosp, Karolinska Inst, Dept Lab Med, Div Clin Microbiol, S-14186 Huddinge, SwedenStockholm Univ, Dept Organ Chem, Arrhenius Lab, S-10691 Stockholm, Sweden
Weintraub, Andrej
[2
]
Widmalm, Goeran
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Stockholm Univ, Dept Organ Chem, Arrhenius Lab, S-10691 Stockholm, SwedenStockholm Univ, Dept Organ Chem, Arrhenius Lab, S-10691 Stockholm, Sweden
Widmalm, Goeran
[1
]
机构:
[1] Stockholm Univ, Dept Organ Chem, Arrhenius Lab, S-10691 Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Dept Lab Med, Div Clin Microbiol, S-14186 Huddinge, Sweden
The O-antigen of the lipopolysaccharide (LPS) from the enteroaggregative Escherichia coli strain 87/D2 has been determined by component analysis together with NMR spectroscopy. The polysaccharide has pentasaccharide repeating units in which all the residues have the galacto-configuration. The repeating unit of the O-antigen, elucidated using the O-deacylated LPS, is branched with the following structure: [GRAPHICS] Analysis of the H-1 NMR spectrum of the LPS revealed O-acetyl groups (similar to 0.7 per repeating unit) distributed over two positions. Subsequent analysis showed that the galactose residue carries acetyl groups at either O-3 or O-4 in a ratio of similar to 2: 1. The international reference strain from E. coli O128ab was investigated and the repeating unit of the O-antigens has the following structure: [GRAPHICS] Analysis of the H-1 NMR spectrum of the LPS revealed O-acetyl groups (approximately one per repeating unit) distributed over two positions. The integrals of the resonances for the O-acetyl groups indicated similarities between the O-antigen from E. coli O128ab and that of E coli strain 87/D2, whereas the O-acetyl substitution pattern in the E coli O128ac O-antigen differed slightly. Enzyme immunoassay using specific anti-E. coli O128ab and anti-E. coli O128ac rabbit sera confirmed the results. (c) 2008 Elsevier Ltd. All rights reserved.