Herrero E, Fairweather N F, Holland I B
J Gen Microbiol. 1982 Feb;128(2):361-9. doi: 10.1099/00221287-128-2-361.
The rates of synthesis of inner and outer membrane proteins of Escherichia coli K12 during inhibition of cell division have been studied. When cell division was inhibited, either by treatment of wild-type cells with the antibiotic clorobiocin (an inhibitor of the B subunit of DNA gyrase) or by a temperature shift of a gyrB-ts mutant, a 40% reduction in the rate of synthesis of total outer membrane protein relative to that of the inner membrane was observed. When a gyrB-ts mutant was shifted to high temperature under conditions which allowed continued cell division, this large reduction in the rate of synthesis of outer membrane protein relative to inner membrane protein was not observed. In contrast to the results obtained with clorobiocin, inhibition of cell division by the beta-lactam antibiotic cefuroxime did not cause any detectable disturbance in the rate of synthesis of either inner or outer membrane protein. This demonstrates that inhibition of septum formation per se does not perturb synthesis of envelope protein. The data obtained are consistent with a model in which the rate of synthesis and therefore expansion of outer membrane is one of many conditions which must be satisfied before septum formation can occur. The results are discussed in relation to such a model, and to previous findings which have shown that the rate of synthesis of outer membrane proteins displays a linear mode with an abrupt doubling in rate at a discrete point in the cell cycle.
研究了大肠杆菌K12细胞分裂受抑制期间内膜和外膜蛋白的合成速率。当通过用抗生素氯生(DNA促旋酶B亚基的抑制剂)处理野生型细胞或通过gyrB-ts突变体的温度转变来抑制细胞分裂时,相对于内膜,观察到总外膜蛋白合成速率降低了40%。当gyrB-ts突变体在允许细胞继续分裂的条件下转移到高温时,未观察到外膜蛋白相对于内膜蛋白合成速率的大幅降低。与用氯生获得的结果相反,β-内酰胺抗生素头孢呋辛对细胞分裂的抑制并未导致内膜或外膜蛋白合成速率出现任何可检测到的干扰。这表明隔膜形成的抑制本身不会扰乱包膜蛋白的合成。所获得的数据与一个模型一致,在该模型中,外膜的合成速率以及因此的扩张是隔膜形成发生之前必须满足的许多条件之一。结合这样一个模型以及先前的研究结果对这些结果进行了讨论,先前的研究结果表明外膜蛋白的合成速率呈现线性模式,在细胞周期的一个离散点速率突然加倍。