Oka T, Fujita H
Antimicrob Agents Chemother. 1978 Oct;14(4):625-7. doi: 10.1128/AAC.14.4.625.
The binding constants of several beta-lactam antibiotics towards penicillin-binding components in Escherichia coli K-12 (Spratt, Eur. J. Biochem. 72:341-352, 1977) and the antibiotic concentrations required to inhibit the peptidoglycan transpeptidase of E. coli 50% were compared. Penicillin-binding component 1B may have been the transpeptidase working in vitro. The structure-activity relationships of beta-lactam antibiotics and the mechanisms of action in E. coli and Bacillus megaterium are discussed.
比较了几种β-内酰胺抗生素与大肠杆菌K-12中青霉素结合成分的结合常数(斯普拉特,《欧洲生物化学杂志》72:341 - 352,1977)以及抑制大肠杆菌肽聚糖转肽酶50%所需的抗生素浓度。青霉素结合成分1B可能是体外起作用的转肽酶。讨论了β-内酰胺抗生素的构效关系以及在大肠杆菌和巨大芽孢杆菌中的作用机制。