Deitz W H, Cook T M, Goss W A
J Bacteriol. 1966 Feb;91(2):768-73. doi: 10.1128/jb.91.2.768-773.1966.
Deitz, William H. (Sterling-Winthrop Research Institute, Rensselaer, N.Y.), Thomas M. Cook, and William A. Goss. Mechanism of action of nalidixic acid on Escherichia coli. III. Conditions required for lethality. J. Bacteriol. 91:768-773. 1966.-Nalidixic acid selectively inhibited deoxyribonucleic acid (DNA) synthesis in cultures of Escherichia coli 15TAU. Protein and ribonucleic acid synthesis were shown to be a prerequisite for the bactericidal action of the drug. This action can be prevented by means of inhibitors at bacteriostatic concentrations. Both chloramphenicol, which inhibits protein synthesis, and dinitrophenol, which uncouples oxidative phosphorylation, effectively prevented the bactericidal action of nalidixic acid on E. coli. The lethal action of nalidixic acid also was controlled by transfer of treated cells to drug-free medium. DNA synthesis resumed immediately upon removal of the drug and was halted immediately by retreatment. These studies indicate that nalidixic acid acts directly on the replication of DNA rather than on the "initiator" of DNA synthesis. The entry of nalidixic acid into cells of E. coli was not dependent upon protein synthesis. Even in the presence of an inhibiting concentration of chloramphenicol, nalidixic acid prevented DNA synthesis by E. coli 15TAU.
迪茨,威廉·H.(纽约州伦斯勒的斯特林-温思罗普研究所)、托马斯·M.库克和威廉·A.戈斯。萘啶酸对大肠杆菌的作用机制。III.致死所需条件。《细菌学杂志》91:768 - 773。1966年。——萘啶酸选择性抑制大肠杆菌15TAU培养物中的脱氧核糖核酸(DNA)合成。蛋白质和核糖核酸合成被证明是该药物杀菌作用的先决条件。这种作用可以通过抑菌浓度的抑制剂来阻止。抑制蛋白质合成的氯霉素和使氧化磷酸化解偶联的二硝基苯酚都能有效阻止萘啶酸对大肠杆菌的杀菌作用。萘啶酸的致死作用也可通过将处理过的细胞转移到无药物培养基中来控制。去除药物后DNA合成立即恢复,重新处理则立即停止。这些研究表明萘啶酸直接作用于DNA复制而非DNA合成的“起始物”。萘啶酸进入大肠杆菌细胞不依赖于蛋白质合成。即使存在抑制浓度的氯霉素,萘啶酸仍能阻止大肠杆菌15TAU的DNA合成。