Mitchell I
Mutat Res. 1978 Aug;54(1):1-16. doi: 10.1016/0165-1161(78)90128-0.
A microbial assay system for mutagenicity was developed in which bacterial cells divided in liquid culture. The statistical and practical problems associated with dividing cells were avoided or reduced, whilst the advantages in precision and reliability resulting from the determination of mutation per colony-forming unit (survivor) and of separating the mutation and selection systems were retained. Seven mutagens, two of which required microsomal activation, were evaluated by this liquid-medium method and by the agar-plate method with two strains of Salmonella typhimurium to determine which assay system was the more sensitive. At highly mutagenic and/or very toxic concentrations of the test substance the liquid-medium assay was markedly more sensitive than the agar-plate assay, but at weakly mutagenic and less toxic concentrations the advantage of the liquid-medium test was reduced; however in only one case was the agar-plate assay obviously the more sensitive. There was a clear indication that the liquid-medium assay would be superior to the agar-plate assay for the detection of mutagenic agents active only at toxic concentrations, and also could be more easily and exactly quantified.
开发了一种用于致突变性检测的微生物检测系统,其中细菌细胞在液体培养中进行分裂。与分裂细胞相关的统计和实际问题得以避免或减少,同时保留了因每个菌落形成单位(存活菌)的突变测定以及突变和选择系统分离而带来的精度和可靠性优势。通过这种液体培养基方法以及使用两株鼠伤寒沙门氏菌的琼脂平板法,对七种诱变剂进行了评估,其中两种需要微粒体激活,以确定哪种检测系统更灵敏。在测试物质具有高致突变性和/或高毒性浓度时,液体培养基检测明显比琼脂平板检测更灵敏,但在弱致突变性和低毒性浓度时,液体培养基检测的优势有所降低;然而,仅在一种情况下琼脂平板检测明显更灵敏。有明确迹象表明,液体培养基检测对于仅在有毒浓度下起作用的诱变剂的检测将优于琼脂平板检测,并且还能够更轻松、准确地进行定量。