A comparative study of the inhibitory effect of Atabrine on R(-) and R(+) strains of Escherichia coli showed that R(+) cells were killed when grown in the presence of Atabrine, whereas R(-) cells were not. It would appear, therefore, that R factor confers sensitivity to Atabrine on the host cells. The "curing" of R factor from R(+) cells by the ultraviolet light-acridine orange method rendered the "cured" cells more resistant than even the parent R(-) cells. The "cured" cells reinfected by R factor were more sensitive than the "cured" cells but less sensitive than the original R(+) cells. After growth once in Atabrine, and even after subcultures in drug-free medium, the growth of R(+) cells in the presence of Atabrine was more rapid than that of the R(-) cells. R(-) cells made resistant by growing them repeatedly in streptomycin, chloramphenicol, tetracycline, and sulfathiazole in succession also showed a higher degree of sensitivity to Atabrine than the original R(-) cells. When mixtures of R(-) and R(+) cells were grown in 120 mug/ml of Atabrine, R(+) cells were killed and the culture consisted predominantly of R(-) cells. A mixture of R(-) and R(+) cells (1:10,000) inoculated into the Atabrine-containing medium and treated 24 hr later with chloramphenicol was completely killed.
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http://dx.doi.org/10.1128/jb.93.1.245-253.1967 | DOI Listing |
Langmuir
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Surface Science Laboratory, Graduate School of Engineering, Toyota Technological Institute, 2-12-1, Hisakata, Tempaku, Nagoya, Aichi 468-8511, Japan.
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