Wolf-Watz H, Normark S
J Bacteriol. 1976 Nov;128(2):580-6. doi: 10.1128/jb.128.2.580-586.1976.
Septum formation and septum separation have been studied in a chain-forming mutant of Escherichia coli K-12 bearing the envA mutation and its parental strain. In comparison to the wild type, the mutant showed a sixfold reduction in the specific activity of the enzyme, N-acetylmuramyl-L-alanine amidase (EC 3.5.1.28), part of which was associated to the outer membrane. Genetic as well as physiological suppression of chain formation resulted in an increase in amidase activity. The addition of N-acetylmuramyl-L-alanyl-D-glutamyl-meso-diaminopimelic acid to growing wild-type cells and to cells bearing the envA mutation caused an inhibition of cell separation and an increased frequency of visible septa. The kinetics of septum formation and separation was followed in chains by the use of ampicillin and nalidixic acid. The latter drug inhibited initiation of new septa but allowed preformed ones to go to cell separation at a rate corresponding to that of steady-state growing cells. Ampicillin treatment, on the other hand, resulted in a more rapid decrease in the frequency of septa. The disparate effects of ampicillin and nalidixic acid were not explained by a difference in amidase activity but could be due to an inhibitory effect of ampicillin on a septal peptidoglycan fusing activity.
在携带envA突变的大肠杆菌K-12链形成突变体及其亲本菌株中,对隔膜形成和隔膜分离进行了研究。与野生型相比,该突变体中N-乙酰胞壁酰-L-丙氨酸酰胺酶(EC 3.5.1.28)的比活性降低了六倍,其中一部分与外膜相关。链形成的遗传抑制和生理抑制均导致酰胺酶活性增加。向生长中的野生型细胞和携带envA突变的细胞中添加N-乙酰胞壁酰-L-丙氨酰-D-谷氨酰-内消旋二氨基庚二酸会抑制细胞分离,并增加可见隔膜的频率。通过使用氨苄青霉素和萘啶酸,跟踪链中隔膜形成和分离的动力学。后一种药物抑制新隔膜的起始,但允许预先形成的隔膜以与稳态生长细胞相应的速率进行细胞分离。另一方面,氨苄青霉素处理导致隔膜频率更快下降。氨苄青霉素和萘啶酸的不同作用不是由酰胺酶活性的差异解释的,而是可能由于氨苄青霉素对隔膜肽聚糖融合活性的抑制作用。