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本文引用的文献

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Infection of Salmonella typhimurium with coliphage Mu d1 (Apr lac): construction of pyr::lac gene fusions.用大肠杆菌噬菌体Mu d1（Apr lac）感染鼠伤寒沙门氏菌：构建pyr::lac基因融合体。
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Antitermination of E. coli rRNA transcription is caused by a control region segment containing lambda nut-like sequences.大肠杆菌核糖体RNA转录的抗终止作用是由一个含有λ nut样序列的控制区片段引起的。
Cell. 1984 Oct;38(3):851-60. doi: 10.1016/0092-8674(84)90280-0.
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Non-smooth mutants of Salmonella typhimurium: differentiation by phage sensitivity and genetic mapping.鼠伤寒沙门氏菌的非光滑突变体：通过噬菌体敏感性和基因图谱进行鉴别
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Cloning of rfaG, B, I, and J genes for glycosyltransferase enzymes for synthesis of the lipopolysaccharide core of Salmonella typhimurium.用于合成鼠伤寒沙门氏菌脂多糖核心的糖基转移酶rfaG、B、I和J基因的克隆。
J Bacteriol. 1985 Jan;161(1):277-84. doi: 10.1128/jb.161.1.277-284.1985.
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鼠伤寒沙门氏菌rfaGBIJ基因座的转录组织

Transcriptional organization of the rfaGBIJ locus of Salmonella typhimurium.

作者信息

Brazas R, Davie E, Farewell A, Rothfield L I

机构信息

Department of Microbiology, University of Connecticut Health Center, Farmington 06032.

出版信息

J Bacteriol. 1991 Oct;173(19):6168-73. doi: 10.1128/jb.173.19.6168-6173.1991.

DOI:10.1128/jb.173.19.6168-6173.1991
PMID:1917851
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC208367/
Abstract

The transcriptional organization of the rfaGBIJ gene cluster of Salmonella typhimurium was studied by using lacZ and cat transcriptional probes. The results indicated that the leftward end of the gene cluster (rfaG-rfaB-rfaI) is an operon that is transcribed from one or more promoters that lie upstream of rfaG. The results further indicated that the product of the rfaH (sfrB) gene acts as a positive regulator of transcription of the entire rfaGBIJ cluster. At least one site required for the RfaH-mediated transcriptional regulation lies within or very close to the upstream promoter.

摘要

利用lacZ和cat转录探针研究了鼠伤寒沙门氏菌rfaGBIJ基因簇的转录组织。结果表明，基因簇的左端（rfaG - rfaB - rfaI）是一个操纵子，它从位于rfaG上游的一个或多个启动子转录。结果还表明，rfaH（sfrB）基因的产物作为整个rfaGBIJ簇转录的正调控因子。RfaH介导的转录调控所需的至少一个位点位于上游启动子内或非常靠近上游启动子。