Mardones G, Venegas A
Laboratorio de Bioquímica, Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Casilla 114-D, Santiago, Chile.
J Microbiol Methods. 2000 May;40(3):199-206. doi: 10.1016/s0167-7012(00)00125-1.
A solid agar plate assay was devised to discriminate bacteriolytic from bacteriostatic activity for a given antibacterial agent. The assay uses a bacterial culture harboring beta-galactosidase enzyme as reporter of cellular lysis. When a drop of bacteriolytic compound is placed on the agar, beta-galactosidase is released from the bacteria to the external solid medium where it hydrolyzes X-Gal substrate analogue, developing a blue halo at the edge of the inhibition growth zone. The assay was successfully evaluated against several antibiotics with well-known mechanism of action. It was found that bacteriostatic compounds consistently did not display blue halo at the inhibition zone.
设计了一种固体琼脂平板试验,以区分给定抗菌剂的溶菌活性和抑菌活性。该试验使用含有β-半乳糖苷酶的细菌培养物作为细胞裂解的报告物。当将一滴溶菌化合物滴在琼脂上时,β-半乳糖苷酶从细菌释放到外部固体培养基中,在那里它水解X-Gal底物类似物,在抑制生长区边缘形成蓝色晕圈。该试验针对几种作用机制已知的抗生素进行了成功评估。结果发现,抑菌化合物在抑制区始终不显示蓝色晕圈。