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大肠杆菌中rfe基因的存在:它们参与O抗原和肠杆菌共同抗原的生物合成。

Presence of rfe genes in Escherichia coli: their participation in biosynthesis of O antigen and enterobacterial common antigen.

作者信息

Schmidt G, Mayer H, Mäkelä P H

出版信息

J Bacteriol. 1976 Aug;127(2):755-62. doi: 10.1128/jb.127.2.755-762.1976.

Abstract

In Salmonella, ilv-linked rfe genes participate in the biosynthesis of the enterobacterial common antigen (CA) as well as of certain types of O antigen (serogroups C1 and L). rff genes, probably in the same cluster with rfe, are required for CA synthesis (P.H. Mäkelä et al., in preparation). Several Escherichia coli strains were studied to determine whether they also have rfe-rff genes that are involved in the synthesis of O antigen and CA, or of CA only. In a first approach, E, coli K-12 F-prime factors carrying the genes ilv and argH or argE and presumably rfe-rff genes were introduced into CA-negative Salmonella mutants that are blocked in CA synthesis because of mutated rfe or rff genes. All resulting ilv+ hybrids were CA positive. In recipients with group C1-derived rfb genes, the synthesis of O6,7-specific antigen was also restored. This result shows that E. coli K-12 has rfe and rff genes providing the functions required in the synthesis of CA and Salmonella 6,7-specific polysaccharide. By introduction of defective rfe regions from suitable Salmonella donors into E. coli O8, 09, and O100 strains, the synthesis of CA as well as of the O-specific polysaccharides was blocked. This indicates that in the E. coli strains tested the rfe genes are involved in the synthesis of both O antigen and CA. This suggestion was confirmed by the finding of E. coli rough mutants that had simultaneously become CA negative. In transduction experiments it could be shown that the appearance of the rough and CA- phenotype was due to a defect in the ilv-linked rfe region.

摘要

在沙门氏菌中,与ilv相关的rfe基因参与肠杆菌共同抗原(CA)以及某些类型O抗原(血清群C1和L)的生物合成。rff基因可能与rfe位于同一基因簇中,是CA合成所必需的(P.H. 梅凯拉等人,正在准备相关研究)。对几种大肠杆菌菌株进行了研究,以确定它们是否也具有参与O抗原和CA合成,或仅参与CA合成的rfe - rff基因。在第一种方法中,将携带ilv和argH或argE基因以及推测的rfe - rff基因的大肠杆菌K - 12 F - 因子导入因rfe或rff基因突变而在CA合成中受阻的CA阴性沙门氏菌突变体中。所有产生的ilv +杂种均为CA阳性。在具有源自C1组的rfb基因的受体中,O6,7特异性抗原的合成也得以恢复。这一结果表明大肠杆菌K - 12具有rfe和rff基因,可提供CA和沙门氏菌6,7特异性多糖合成所需的功能。通过将来自合适沙门氏菌供体的缺陷rfe区域导入大肠杆菌O8、O9和O100菌株中,CA以及O特异性多糖的合成均被阻断。这表明在所测试的大肠杆菌菌株中,rfe基因参与O抗原和CA的合成。大肠杆菌粗糙突变体同时变为CA阴性这一发现证实了这一推测。在转导实验中可以表明,粗糙和CA - 表型的出现是由于ilv相关rfe区域的缺陷所致。

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