Karamova N S, Il'inskaia O N, Ivanchenko O B
Genetika. 1994 Jul;30(7):898-902.
Mutagenic activity of 2,4,6-trinitrotoluene (2,4,6-TNT) and one of its derivatives, 2,4-diamino-6-nitrotoluene (2,4-DA-6-NT) was studied in the Ames test using the Salmonella typhimurium tester strains TA98, TA100, TA100NR (deficient in classical nitroreductases), and TA100/1, 8DNP (deficient in O-acetyltransferase). The number of revertants was significantly increased by 2,4,6-TNT, in comparison with that of spontaneous revertants. Base pair substitutions were preferentially induced by 2,4,6-TNT. The mutagenic effect of this compound was virtually altered by in vitro metabolic activation with the S9 fraction of human placenta. Neither 2,4,6-TNT nor 2,4-DA-6-NT exhibited mutagenic activity in the strains TA 100NR and TA 100/1,8DNP. Based on the results obtained, it is concluded that the mutagenic potential of 2,4,6-TNT is determined by its metabolites that form during bacterial metabolism. Bacterial nitroreductases and O-acetyltransferases are the key activators of this compound to form the ultimate mutagens.
使用鼠伤寒沙门氏菌测试菌株TA98、TA100、TA100NR(缺乏经典硝基还原酶)和TA100/1,8DNP(缺乏O-乙酰转移酶),在艾姆斯试验中研究了2,4,6-三硝基甲苯(2,4,6-TNT)及其衍生物之一2,4-二氨基-6-硝基甲苯(2,4-DA-6-NT)的致突变活性。与自发回复突变体相比,2,4,6-TNT显著增加了回复突变体的数量。2,4,6-TNT优先诱导碱基对替换。该化合物的致突变作用实际上通过用人胎盘S9组分进行体外代谢活化而改变。2,4,6-TNT和2,4-DA-6-NT在TA 100NR和TA 100/1,8DNP菌株中均未表现出致突变活性。根据所得结果得出结论,2,4,6-TNT的致突变潜力由其在细菌代谢过程中形成的代谢产物决定。细菌硝基还原酶和O-乙酰转移酶是该化合物形成最终诱变剂的关键激活剂。