Guarneros G, Machado G, Guzmán P, Garay E
Department of Genetics and Molecular Biology, Centro de Investigación y de Estudios Avanzados del Instituto, Politécnico Nacional, Mexico City, Mexico.
J Bacteriol. 1987 Nov;169(11):5188-92. doi: 10.1128/jb.169.11.5188-5192.1987.
The Escherichia coli rap mutant does not support the growth of bacteriophage lambda (D. Henderson and J. Weil, Virology 71:546-559, 1976). We located the rap site at 26 min in the E. coli genetic map and determined the gene order fadR-rap-supF-trp from our transduction experiments. Plasmid pHO1 harbors a 5.6-kilobase-pair segment of the E. coli chromosome which contains the pth gene (B. Hove-Jensen, Mol. Gen. Genet. 201:269-276, 1985). This plasmid complemented rap bacteria, suggesting that it carries the dominant allele rap+. Subcloning experiments reduced the rap-complementing segment to 1.5 kilobase pairs. This segment still contained pth; thus, both loci are tightly linked. The lit mutations that inhibit phage T4 growth in E. coli are located nearby at 25 min (W. Cooley, K. Sirotkin, R. Green, and L. Snyder, J. Bacteriol. 140:83-91, 1979). We showed that rap and lit mutations are phenotypically and genetically different.
大肠杆菌rap突变体不能支持噬菌体λ的生长(D. 亨德森和J. 韦尔,《病毒学》71:546 - 559,1976年)。我们将rap位点定位在大肠杆菌遗传图谱的26分钟处,并通过转导实验确定了基因顺序为fadR - rap - supF - trp。质粒pHO1含有一段5.6千碱基对的大肠杆菌染色体片段,其中包含pth基因(B. 霍夫 - 延森,《分子与普通遗传学》201:269 - 276,1985年)。该质粒互补rap细菌,表明它携带显性等位基因rap⁺。亚克隆实验将rap互补片段减少到1.5千碱基对。该片段仍包含pth;因此,两个位点紧密连锁。抑制噬菌体T4在大肠杆菌中生长的lit突变位于附近的25分钟处(W. 库利、K. 西罗特金、R. 格林和L. 斯奈德,《细菌学杂志》140:83 - 91,1979年)。我们表明rap和lit突变在表型和遗传上是不同的。