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福氏志贺菌6型rfb区域在大肠杆菌K-12中的分子克隆与遗传分析。

Molecular cloning and genetic analysis of the rfb region from Shigella flexneri type 6 in Escherichia coli K-12.

作者信息

Cheah K C, Beger D W, Manning P A

机构信息

Department of Microbiology and Immunology, University of Adelaide, South Australia.

出版信息

FEMS Microbiol Lett. 1991 Oct 1;67(2):213-8. doi: 10.1016/0378-1097(91)90356-f.

Abstract

The rfb gene cluster which determines the biosynthesis of the Shigella flexneri serotype 6 O-antigen specificity has been cloned in pHC79, generating plasmids pPM3115 and pPM3116. These plasmids mediate expression, in Escherichia coli K-12, of lipopolysaccharides (LPS) immunologically similar to the S. flexneri type 6 LPS as judged by SDS-PAGE and Western-immunoblot analysis using S. flexneri type 6 specific antisera. Thus, unlike other S. flexneri serotypes, no additional loci are required for serotype specificity. This expression is independent of E. coli K-12 rfb genes. Southern-hybridization analysis using the 16.2-kb BglII probe from S. flexneri type 6 rfb region detected very little sequence homology in S. flexneri serotypes 1-5, however, some homology was detected with E. coli O2 and O18, but not in E. coli 0101 strains, Salmonella and Vibrio cholerae.

摘要

决定弗氏志贺菌6型O抗原特异性生物合成的rfb基因簇已克隆到pHC79中,产生了质粒pPM3115和pPM3116。通过SDS-PAGE和使用弗氏志贺菌6型特异性抗血清的Western免疫印迹分析判断,这些质粒在大肠杆菌K-12中介导了与弗氏志贺菌6型脂多糖(LPS)免疫相似的LPS表达。因此,与其他弗氏志贺菌血清型不同,血清型特异性不需要额外的基因座。这种表达独立于大肠杆菌K-12的rfb基因。使用来自弗氏志贺菌6型rfb区域的16.2 kb BglII探针进行的Southern杂交分析在弗氏志贺菌1-5型血清型中检测到的序列同源性非常少,然而,在大肠杆菌O2和O18中检测到了一些同源性,但在大肠杆菌0101菌株、沙门氏菌和霍乱弧菌中未检测到。

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