Rogers H J, Forsberg C W
J Bacteriol. 1971 Dec;108(3):1235-43. doi: 10.1128/jb.108.3.1235-1243.1971.
The rapid lysis of Bacillus licheniformis NCTC 6346 and B. subtilis 168 trp caused by vancomycin and d-cycloserine can be inhibited by stopping protein synthesis. Protein synthesis must be stopped for more than one doubling time of the cells before addition of wall inhibitors. Poorly lytic mutants (lyt(-)) of B. licheniformis required 10 to 20 times the concentration of vancomycin or cycloserine to be added to growing cultures to cause even slow lysis. At lower concentrations growth of the mutants is stopped, but the bacteria remain fully viable. Sensitivity of mucopeptide synthesis to vancomycin is the same in both mutants and parent. Sensitivity to the action of d-cycloserine is slightly less in the mutant than in the parent.
由万古霉素和d-环丝氨酸引起的地衣芽孢杆菌NCTC 6346和枯草芽孢杆菌168 trp的快速裂解可通过停止蛋白质合成来抑制。在添加细胞壁抑制剂之前,必须停止蛋白质合成超过细胞的一个倍增时间。地衣芽孢杆菌的低裂解突变体(lyt(-))需要在生长培养物中添加比正常情况高10至20倍浓度的万古霉素或环丝氨酸才能引起即使是缓慢的裂解。在较低浓度下,突变体的生长会停止,但细菌仍保持完全存活。突变体和亲本中粘肽合成对万古霉素的敏感性相同。突变体对d-环丝氨酸作用的敏感性略低于亲本。