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通过嵌入性化合物消除R因子R1中的抗性决定簇。

Elimination of resistance determinants from R-factor R1 by intercalative compounds.

作者信息

Hahn F E, Ciak J

出版信息

Antimicrob Agents Chemother. 1976 Jan;9(1):77-80. doi: 10.1128/AAC.9.1.77.

Abstract

Eighteen deoxyribonucleic acid (DNA)-complexing compounds, among them 15 intercalative substances, and, additionally, nalidixic acid eliminated with different frequencies four antibiotic resistance determinants from the R-factor R1, carried by Salmonella typhimurium. Eliminating concentrations did not inhibit growth of the bacteria. The most active compound was "nitroacridine II" {1-diethylamino-3-[(6-nitro-9-acridinyl)amino]propanol}. When 14 compounds which had been tested at a standard concentration of 10(-4) M were listed according to decreasing activities of elimination of the four resistance determinants, a nearly consistent activity sequence was revealed. Frequencies of elimination of the kanamycin resistance determinant correlated directly with the binding of compounds to DNA, i.e., with end points of their displacement of methyl green from the methyl green-DNA complex. We propose that the observed eliminations resulted from selective toxicity for plasmidic template DNA and inhibitions of R-factor replication.

摘要

18种与脱氧核糖核酸(DNA)结合的化合物,其中15种为嵌入性物质,此外,萘啶酸以不同频率消除了鼠伤寒沙门氏菌携带的R因子R1上的4种抗生素抗性决定簇。消除浓度并未抑制细菌生长。活性最高的化合物是“硝基吖啶II”{1-二乙氨基-3-[(6-硝基-9-吖啶基)氨基]丙醇}。当按照消除4种抗性决定簇的活性递减列出14种在标准浓度10(-4)M下测试过的化合物时,发现了一个几乎一致的活性序列。卡那霉素抗性决定簇的消除频率与化合物与DNA的结合直接相关,即与它们从甲基绿-DNA复合物中置换甲基绿的终点相关。我们认为观察到的消除是由于对质粒模板DNA的选择性毒性和对R因子复制的抑制所致。

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