Swenson D L, Clegg S
Department of Microbiology, University of Iowa College of Medicine, Iowa City 52242.
J Bacteriol. 1992 Dec;174(23):7697-704. doi: 10.1128/jb.174.23.7697-7704.1992.
Regulation of the gene, fimA, encoding the major fimbrial subunit of S. typhimurium S6704 was examined by using a lambda fimA-lacZ lysogen. Transformation of the lambda fimA-lacZ lysogen with various derivatives of the recombinant plasmid that encodes type 1 fimbrial expression, pISF101, indicated that two regions of this plasmid alter beta-galactosidase production. One plasmid is a deletion resulting in the loss of a 28-kDa polypeptide downstream of fimA, while the other plasmid encodes a 24- and a 27-kDa polypeptide. Northern (RNA) blot analyses indicated that the steady-state fimA mRNA levels of these transformants were high. In addition, phenotypic expression of type 1 fimbriae by agar-grown cultures is observed only in those transformants bearing plasmids which show increased beta-galactosidase and fimA mRNA levels.
利用λfimA - lacZ溶原菌对编码鼠伤寒沙门氏菌S6704主要菌毛亚基的基因fimA进行了调控研究。用编码1型菌毛表达的重组质粒pISF101的各种衍生物转化λfimA - lacZ溶原菌,结果表明该质粒的两个区域会改变β - 半乳糖苷酶的产生。一种质粒是缺失型,导致fimA下游一个28 kDa多肽缺失,而另一种质粒编码一个24 kDa和一个27 kDa的多肽。Northern(RNA)印迹分析表明这些转化体中fimA的稳态mRNA水平很高。此外,仅在那些携带质粒且β - 半乳糖苷酶和fimA mRNA水平升高的转化体的琼脂培养物中观察到1型菌毛的表型表达。