Boyle J V, Goss W A, Cook T M
J Bacteriol. 1967 Nov;94(5):1664-71. doi: 10.1128/jb.94.5.1664-1671.1967.
Prior treatment of Escherichia coli with nalidixic acid in nutritionally complete medium altered the subsequent pattern of deoxyribonucleic acid (DNA) synthesis normally observed in nutritionally deficient medium. Transfer of E. coli 15 TAU to an amino acid- and pyrimidine-deficient medium usually resulted in a 40 to 50% increase in DNA content. Previous treatment with nalidixic acid caused a 200 to 300% increase in DNA content under these conditions. The extent of this DNA synthesis depended on the duration of prior exposure to nalidixic acid. The maximal rate of synthesis was obtained after a 40- to 60-min exposure to nalidixic acid and was two to three times that of the control. The induction of this excessive DNA synthesis was prevented by chloramphenicol or phenethyl alcohol, but the synthesis of this DNA was only partially sensitive to these agents. With E. coli TAU-bar, the rate of DNA synthesis, after removal of nalidixic acid, was similar to that of E. coli 15 TAU, but the maximal amount of DNA synthesized was 180 to 185% of that initially present. Cesium chloride density gradient analysis demonstrated that DNA synthesis after removal of nalidixic acid occurs by a semiconservative mode of replication. The density distribution of this DNA was similar to that obtained after thymine starvation. These results suggest that nalidixic acid treatment may induce additional sites for DNA synthesis in E.coli.
在营养完全的培养基中用萘啶酸预先处理大肠杆菌,会改变随后在营养缺陷型培养基中正常观察到的脱氧核糖核酸(DNA)合成模式。将大肠杆菌15 TAU转移到氨基酸和嘧啶缺陷型培养基中,通常会导致DNA含量增加40%至50%。在这些条件下,用萘啶酸预先处理会使DNA含量增加200%至300%。这种DNA合成的程度取决于预先接触萘啶酸的持续时间。在接触萘啶酸40至60分钟后可获得最大合成速率,是对照的两到三倍。氯霉素或苯乙醇可阻止这种过量DNA合成的诱导,但这种DNA的合成仅对这些试剂部分敏感。对于大肠杆菌TAU-bar,去除萘啶酸后DNA合成速率与大肠杆菌15 TAU相似,但合成的最大DNA量是最初存在量的180%至185%。氯化铯密度梯度分析表明,去除萘啶酸后的DNA合成通过半保留复制模式进行。这种DNA的密度分布与胸腺嘧啶饥饿后获得的相似。这些结果表明,萘啶酸处理可能会在大肠杆菌中诱导额外的DNA合成位点。