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肠道细菌的耐药性。VII. R因子与四环素敏感突变体的重组。

Drug resistance of enteric bacteria. VII. Recombination of R factors with tetracycline-sensitive mutants.

作者信息

Hashimoto H, Mitsuhashi S

出版信息

J Bacteriol. 1966 Nov;92(5):1351-6. doi: 10.1128/jb.92.5.1351-1356.1966.

Abstract

Hashimoto, Hajime (Gunma University, Maebashi, Japan), and Susumu Mitsuhashi. Drug resistance of enteric bacteria. VII. Recombination of R factors with tetracycline-sensitive mutants. J. Bacteriol. 92:1351-1356. 1966.-The transmissible drug-resistance factor R is able to confer resistance to tetracycline (TC), chloramphenicol (CM), streptomycin (SM), and sulfonamide (SA) on a host bacterium when infected by cell-to-cell contact. Tetracycline-sensitive mutants were isolated from either CM- or SM-sensitive mutants of an R factor. Among 30 mutants isolated, 10 were point mutants which could recombine with each other, forming recombinant R factors able to grow on plates containing 50 mug/ml of TC. The recombination frequency of TC-resistant recombinants was 10(-2) to 10(-3) in bacterial cells carrying two types of TC-sensitive R factors by superinfection with both factors. Segregational patterns of the various markers on the R factor, i.e., chl, str, sul, and m, the locus determining R mating, and their linkage order, were investigated among TC-resistant recombinants of the R factor. When TC was used as the selective drug, the tet locus mapped on the R factor as an end marker. In view of the fact that these results are inconsistent with the linkage order of various markers reported previously, a circular genetic structure for the R factor which includes five tet-s and three chl-s loci is presented.

摘要

桥本肇(日本前桥市群马大学)与三桥进。肠道细菌的耐药性。VII. R因子与四环素敏感突变体的重组。《细菌学杂志》92:1351 - 1356。1966年。——可传递的耐药因子R在通过细胞间接触感染宿主细菌时,能够使其对四环素(TC)、氯霉素(CM)、链霉素(SM)和磺胺类药物(SA)产生耐药性。从R因子的CM敏感突变体或SM敏感突变体中分离出四环素敏感突变体。在分离出的30个突变体中,有10个是点突变体,它们能够相互重组,形成能在含有50微克/毫升TC的平板上生长的重组R因子。在携带两种类型四环素敏感R因子的细菌细胞中,通过两种因子的双重感染,四环素抗性重组体的重组频率为10⁻²至10⁻³。在R因子的四环素抗性重组体中,研究了R因子上各种标记(即chl、str、sul和m,决定R交配的位点)的分离模式及其连锁顺序。当使用TC作为选择药物时,tet位点在R因子上作为末端标记定位。鉴于这些结果与先前报道的各种标记的连锁顺序不一致,提出了一种包括五个tet - s和三个chl - s位点的R因子的环状遗传结构。

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