Synthesis of lipopolysaccharide O-antigens by ABC transporter-dependent pathways

被引:120
|
作者
Greenfield, Laura K. [1 ]
Whitfield, Chris [1 ]
机构
[1] Univ Guelph, Dept Mol & Cellular Biol, Guelph, ON N1G 2W1, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
Lipopolysaccharide; O-Polysaccharide; ATP-binding cassette transporter; Escherichia coli O9a; Klebsiella pneumoniae O2a; GRAM-NEGATIVE BACTERIA; ESCHERICHIA-COLI K-12; KLEBSIELLA-PNEUMONIAE SEROTYPE-O1; RFB GENE CLUSTERS; D-GALACTAN-I; ENTEROBACTERIAL COMMON ANTIGEN; BINDING CASSETTE TRANSPORTER; POLYACRYLAMIDE GEL-ELECTROPHORESIS; O1K2; NCTC-5055; LIPOPOLYSACCHARIDE; ACID-SEQUENCE SIMILARITIES;
D O I
10.1016/j.carres.2012.02.027
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
The O-polysaccharide (O-PS; O-antigen) of bacterial lipopolysaccharides is made up of repeating units of one or more sugar residues and displays remarkable structural diversity. Despite the structural variations, there are only three strategies for O-PS assembly. The ATP-binding cassette (ABC)-transporter-dependent mechanism of O-PS biosynthesis is widespread. The Escherichia coli O9a and Klebsiella pneumoniae O2a antigens provide prototypes, which are distinguished by the fine details that link glycan polymerization and chain termination at the cytoplasmic face of the inner membrane to its export via the ABC transporter. Here, we describe the current understanding of these processes. Since glycoconjugate assembly complexes that utilize an ABC transporter-dependent pathway are widespread among the bacterial kingdom, the models described here are expected to extend beyond O-PS biosynthesis systems. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:12 / 24
页数:13
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