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大肠杆菌09抗原的生物合成。rfe突变体的核心结构作为组装机制的指示。

Biosynthesis of the 09 antigen of Escherichia coli. Core structure of rfe mutant as indication of assembly mechanism.

作者信息

Weisgerber C, Jann B, Jann K

出版信息

Eur J Biochem. 1984 May 2;140(3):553-6. doi: 10.1111/j.1432-1033.1984.tb08137.x.

DOI:10.1111/j.1432-1033.1984.tb08137.x
PMID:6202518
Abstract

The chemical structure of the outer (hexose) regions of the core oligosaccharide from Escherichia coli 09 with the complete R1 core, and from a R1-derived rfe mutant were analyzed using compositional analysis, methylation and gas chromatography/mass spectrometry. It was found that, in contrast to the branched outer region of the R1 core, the outer region of the core from the rfe mutant lacked terminal glucose and was linear. These results are in agreement with recent findings on the biosynthesis of the 09 antigen. They suggest a cotransfer of glucose with the 09-specific mannan to a 'pre-core' lacking terminal glucose, as the assembly (translocation) step in the 09 antigen synthesis. Thus it is suggested that the initiation of O-chain synthesis (by the formation of an acceptor glucolipid ) and the termination of core synthesis are closely correlated. In conjunction with previous biochemical data, the analytical results presented here indicate a novel core synthesis.

摘要

利用成分分析、甲基化以及气相色谱/质谱分析法,对具有完整R1核心的大肠杆菌O9核心寡糖的外部(己糖)区域,以及一个源自R1的rfe突变体的核心寡糖外部区域的化学结构进行了分析。结果发现,与R1核心的分支状外部区域不同,rfe突变体核心的外部区域缺乏末端葡萄糖且呈线性。这些结果与最近关于O9抗原生物合成的研究结果一致。它们表明,在O9抗原合成的组装(易位)步骤中,葡萄糖与O9特异性甘露聚糖共同转移至缺乏末端葡萄糖的“前核心”。因此,有人提出O链合成的起始(通过形成受体糖脂)与核心合成的终止密切相关。结合先前的生化数据,此处给出的分析结果表明了一种新的核心合成方式。

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1
Biosynthesis of the 09 antigen of Escherichia coli. Core structure of rfe mutant as indication of assembly mechanism.大肠杆菌09抗原的生物合成。rfe突变体的核心结构作为组装机制的指示。
Eur J Biochem. 1984 May 2;140(3):553-6. doi: 10.1111/j.1432-1033.1984.tb08137.x.
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引用本文的文献

1
A single amino acid substitution in a mannosyltransferase, WbdA, converts the Escherichia coli O9 polysaccharide into O9a: generation of a new O-serotype group.甘露糖基转移酶WbdA中的单个氨基酸取代将大肠杆菌O9多糖转化为O9a:一个新的O血清型组的产生。
J Bacteriol. 2000 May;182(9):2567-73. doi: 10.1128/JB.182.9.2567-2573.2000.
2
Expression of the O9 polysaccharide of Escherichia coli: sequencing of the E. coli O9 rfb gene cluster, characterization of mannosyl transferases, and evidence for an ATP-binding cassette transport system.大肠杆菌O9多糖的表达:大肠杆菌O9 rfb基因簇的测序、甘露糖基转移酶的特性分析以及ATP结合盒转运系统的证据
J Bacteriol. 1995 Apr;177(8):2178-87. doi: 10.1128/jb.177.8.2178-2187.1995.
3
Role of the rfe gene in the synthesis of the O8 antigen in Escherichia coli K-12.
rfe基因在大肠杆菌K-12中O8抗原合成中的作用。
J Bacteriol. 1994 May;176(10):2877-84. doi: 10.1128/jb.176.10.2877-2884.1994.
4
Partial deletion of the cloned rfb gene of Escherichia coli O9 results in synthesis of a new O-antigenic lipopolysaccharide.大肠杆菌O9克隆rfb基因的部分缺失导致一种新的O抗原脂多糖的合成。
J Bacteriol. 1989 Jul;171(7):3629-33. doi: 10.1128/jb.171.7.3629-3633.1989.
5
Biosynthesis of enterobacterial common antigen requires dTDPglucose pyrophosphorylase determined by a Salmonella typhimurium rfb gene and a Salmonella montevideo rfe gene.肠杆菌共同抗原的生物合成需要由鼠伤寒沙门氏菌rfb基因和蒙得维的亚沙门氏菌rfe基因所决定的dTDP葡萄糖焦磷酸化酶。
J Bacteriol. 1986 Nov;168(2):715-21. doi: 10.1128/jb.168.2.715-721.1986.
6
Monoclonal antibodies to enterobacterial common antigen and to Escherichia coli lipopolysaccharide outer core: demonstration of an antigenic determinant shared by enterobacterial common antigen and E. coli K5 capsular polysaccharide.抗肠道细菌共同抗原和大肠杆菌脂多糖外核的单克隆抗体:证明肠道细菌共同抗原与大肠杆菌K5荚膜多糖共有的抗原决定簇。
Infect Immun. 1985 Nov;50(2):459-66. doi: 10.1128/iai.50.2.459-466.1985.