García-del Portillo F, Pisabarro A G, de la Rosa E J, de Pedro M A
J Bacteriol. 1987 Jun;169(6):2410-6. doi: 10.1128/jb.169.6.2410-2416.1987.
Resting cells of Escherichia coli are able to initiate growth and murein biosynthesis in the presence of beta-lactam antibiotics binding to penicillin-binding proteins (PBPs) 1a and 1b (E. J. de la Rosa, M. A. de Pedro, and D. Vázquez, Proc. Natl. Acad. Sci. USA 82:5632-5635, 1985). Under these conditions, cells elongate normally until they approach the first doubling in mass, the time at which cell lysis starts. Assuming that coupling between DNA replication and cell division both in cells starting growth and in growing cells is essentially similar, triggering of the lytic response in the beta-lactam-treated cells coincides with the termination of the first round of DNA replication. This coincidence suggests that both events are interrelated. We investigated this possibility by studying the initiation of growth in cultures of wild-type strains and in cell division mutants treated with beta-lactams inhibiting PBPs 1a and 1b and with the DNA replication inhibitor nalidixic acid. Addition of nalidixic acid, even late in the first cell cycle, prevented the lytic response of the cells to the blockade of PBPs 1a and 1b. The effect of nalidixic acid is more likely due to its action on DNA replication itself than to its indirect inhibitory effect on cell division or to its ability to induce the SOS system of the cell. These observations favor the idea that the cell wall biosynthetic machinery might be modulated by DNA replication at precise periods during cell growth.
在存在与青霉素结合蛋白(PBPs)1a和1b结合的β-内酰胺抗生素的情况下,大肠杆菌的静息细胞能够启动生长和胞壁质生物合成(E. J. 德拉罗萨、M. A. 德佩德罗和D. 巴斯克斯,《美国国家科学院院刊》82:5632 - 5635,1985年)。在这些条件下,细胞正常伸长,直到接近质量首次翻倍,此时细胞裂解开始。假设在开始生长的细胞和正在生长的细胞中,DNA复制与细胞分裂之间的偶联基本相似,那么β-内酰胺处理的细胞中裂解反应的触发与第一轮DNA复制的终止同时发生。这种巧合表明这两个事件是相互关联的。我们通过研究野生型菌株培养物以及用抑制PBPs 1a和1b的β-内酰胺以及DNA复制抑制剂萘啶酸处理的细胞分裂突变体中的生长起始来研究这种可能性。加入萘啶酸,即使在第一个细胞周期后期,也能阻止细胞对PBPs 1a和1b阻断的裂解反应。萘啶酸的作用更可能是由于其对DNA复制本身的作用,而不是对细胞分裂的间接抑制作用或诱导细胞SOS系统的能力。这些观察结果支持这样一种观点,即细胞壁生物合成机制可能在细胞生长的精确时期受到DNA复制的调节。