McCarroll N E, Piper C E, Keech B H
Environ Mutagen. 1981;3(4):429-44. doi: 10.1002/em.2860030404.
We have devised a microsuspension assay utilizing E coli indicator strains WP2, WP2 uvrA, WP67, CM611, WP100, W3110polA+, and p3478 pola- for the detection of chemically-induced preferential kill of repair-deficient strains. Data are presented from tests of 77 compounds representing a wide range of chemical classes which demonstrate the efficiency of the E coli microsuspension assay as both a qualitative and quantitative screen of DNA-modifying activity. Furthermore, the use of a battery of indicator strains lacking different repair systems offers the advantage of providing preliminary information concerning the mechanism of DNA damage induction by a test agent.
我们设计了一种微悬浮试验,利用大肠杆菌指示菌株WP2、WP2 uvrA、WP67、CM611、WP100、W3110polA+和p3478 pola-来检测化学诱导的修复缺陷菌株的优先杀伤作用。文中展示了对77种代表广泛化学类别的化合物进行测试的数据,这些数据证明了大肠杆菌微悬浮试验作为DNA修饰活性定性和定量筛选方法的有效性。此外,使用一系列缺乏不同修复系统的指示菌株具有优势,能够提供有关受试剂诱导DNA损伤机制的初步信息。