The structure of the linkage between the O-specific polysaccharide and the core region of the lipopolysaccharide from Salmonella enterica serovar Typhimurium revisited

被引:40
作者
Olsthoorn, MA
Petersen, BO
Duus, J
Haverkamp, J
Thomas-Oates, JE
Bock, K
Holst, O
机构
[1] Res Ctr Borstel, Ctr Med & Biosci, Div Med & Biochem Microbiol, D-23845 Borstel, Germany
[2] Univ Utrecht, Dept Biomol Mass Spect, Bijvoet Ctr Biomol Res, NL-3508 TC Utrecht, Netherlands
[3] Carlsberg Lab, Dept Chem, Valby, Denmark
[4] Univ Manchester, Dept Chem, Michael Barber Ctr Mass Spect, Manchester M60 1QD, Lancs, England
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2000年 / 267卷 / 07期
关键词
lipopolysaccharide; mass spectrometry; NMR spectroscopy; O-specific polysaccharide; Salmonella enterica sv; Typhimurium;
D O I
10.1046/j.1432-1327.2000.01205.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salmonella enterica sv. Typhimurium strain 1135 possesses smooth(S)-form lipopolysaccharide (LPS). Although the structures of the core region and the O-specific polysaccharide were investigated intensively between the 1960s and the 1980s, the structure of the linkage region between the O-chain and the core was not elucidated unequivocally. By using modern MS and high-field NMR spectroscopy for analysis of the isolated carbohydrate backbone of the LPS, it has been shown that it is a beta-d-Galp residue that links the first repeating unit of the O-specific polysaccharide to O-4 of the last d-Glcp residue of the core region. Interestingly, this particular d-Galp residue is alpha-linked in all following repeating units. The data are discussed with regard to the ligation of O-specific polysaccharide and core region during LPS biosynthesis.
引用
收藏
页码:2014 / 2027
页数:14
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