Wade M J, Moyer J W, Hine C H
Mutat Res. 1979 Apr;66(4):367-71. doi: 10.1016/0165-1218(79)90047-8.
The mutagenicity of a series of 13 epoxide compounds was studied using a bacterial plate assay system. The histidine-dependent tester strains TA98 (for frameshift mutagens) and TA100 (for base-pair substitution mutagens) of Salmonella typhimurium were used. Mutagenicity was evaluated both with and without the additon of rat liver microsomal extract. Dieldrin, diglycidyl ether of bis phenol A and 3 of its homologues were not mutagenic. Allyl glycidyl ether, n-butyl glycidyl ether, vinly cyclohexene diepoxide, glycidol, glycidal-dehyde, diglycidyl ether, diepoxybutane and diglycidyl ether of substituted glycerine were mutagenic in the TA100 strain, causing reversion of the bacteria to histidine independence. Dose-reponse curves of the mutagenicity of the latter 4 compounds were obtained. On a molar basis, glycidaldehyde was about 20-50 times more potent in producing mutation that were the other 3 epoxides in the dose-response test. In general, the mutagenicity of the epoxides was not enhanced or diminished by the addition of microsomal extract.
使用细菌平板检测系统研究了一系列13种环氧化合物的致突变性。采用了鼠伤寒沙门氏菌的组氨酸依赖型测试菌株TA98(用于移码诱变剂)和TA100(用于碱基对取代诱变剂)。在添加和不添加大鼠肝微粒体提取物的情况下评估致突变性。狄氏剂、双酚A的二缩水甘油醚及其3种同系物没有致突变性。烯丙基缩水甘油醚、正丁基缩水甘油醚、乙烯基环己烯二环氧化物、缩水甘油、缩水甘油醛、二缩水甘油醚、1,4 - 丁二醇二缩水甘油醚和取代甘油的二缩水甘油醚在TA100菌株中具有致突变性,导致细菌回复为不依赖组氨酸。获得了后4种化合物致突变性的剂量 - 反应曲线。在剂量 - 反应试验中,以摩尔计,缩水甘油醛产生突变的效力比其他3种环氧化物高约20 - 50倍。一般来说,添加微粒体提取物不会增强或减弱环氧化物的致突变性。