Williamson R, Tomasz A
Eur J Biochem. 1985 Sep 16;151(3):475-83. doi: 10.1111/j.1432-1033.1985.tb09126.x.
Growing cultures of an autolysis-defective pneumococcal mutant were exposed to [3H]benzylpenicillin at various multiples of the minimal inhibitory concentration and incubated until the growth of the cultures was halted. During the process of growth inhibition, we determined the rates and degree of acylation of the five penicillin-binding proteins (PBPs) and the rates of peptidoglycan incorporation, protein synthesis, and turbidity increase. The time required for the onset of the inhibitory effects of benzylpenicillin was inversely related to the concentration of the antibiotic, and inhibition of peptidoglycan incorporation always preceded inhibition of protein synthesis and growth. When cultures first started to show the onset of growth inhibition, the same characteristic fraction of each PBP was in the acylated form in all cases, irrespective of the antibiotic concentration. Apparently, saturation of one or more PBPs with the antibiotic beyond these threshold levels is needed to bring about interference with normal peptidoglycan production and cellular growth. Although it was not possible to correlate the inhibition of cell wall synthesis or cell growth with the degree of acylation (percentage saturation) of any single PBP, there was a correlation between the amount of peptidoglycan synthesized and the actual amount of PBP 2b that was not acylated. In cultures exposed to benzylpenicillin concentrations greater than eight times the minimal inhibitory concentration, the rates of peptidoglycan incorporation underwent a rapid decline when bacterial growth stopped. However, in cultures exposed to lower concentrations of benzylpenicillin (one to six times the minimal inhibitory concentration) peptidoglycan synthesis continued at constant rate for prolonged periods, after the turbidity had ceased to increase. We conclude that inhibition of bacterial growth does not require a complete inhibition or even a major decline in the rate of peptidoglycan incorporation. Rather, inhibition of growth must be caused by an as yet undefined process that stops cell division when the rate of incorporation of peptidoglycan (or synthesis of protein) falls below a critical value.
将自溶缺陷型肺炎球菌突变体的培养物在不同的最低抑菌浓度倍数下暴露于[3H]苄青霉素,并孵育直至培养物的生长停止。在生长抑制过程中,我们测定了五种青霉素结合蛋白(PBPs)的酰化速率和程度以及肽聚糖掺入、蛋白质合成和浊度增加的速率。苄青霉素抑制作用开始所需的时间与抗生素浓度呈负相关,肽聚糖掺入的抑制总是先于蛋白质合成和生长的抑制。当培养物首次开始显示出生长抑制的开始时,在所有情况下,每种PBP的相同特征部分都处于酰化形式,与抗生素浓度无关。显然,需要使一种或多种PBPs与抗生素的饱和度超过这些阈值水平,才能干扰正常的肽聚糖产生和细胞生长。虽然不可能将细胞壁合成或细胞生长的抑制与任何单个PBP的酰化程度(饱和百分比)相关联,但合成的肽聚糖量与未酰化的PBP 2b的实际量之间存在相关性。在暴露于大于最低抑菌浓度八倍的苄青霉素浓度的培养物中,当细菌生长停止时,肽聚糖掺入速率迅速下降。然而,在暴露于较低浓度苄青霉素(最低抑菌浓度的一至六倍)的培养物中,在浊度停止增加后,肽聚糖合成在长时间内以恒定速率继续。我们得出结论,细菌生长的抑制并不需要肽聚糖掺入速率的完全抑制甚至大幅下降。相反,生长的抑制必须由一个尚未明确的过程引起,当肽聚糖掺入(或蛋白质合成)速率低于临界值时,该过程会停止细胞分裂。