Frantz S W, Sinsheimer J E
Mutat Res. 1981 Sep;90(1):67-78. doi: 10.1016/0165-1218(81)90051-3.
The mutagenicity of 12 cycloaliphatic epoxides was investigated using the Ames Salmonella assay without the addition of liver homogenate fractions. Base-pair substitution mutagenic activity was detected for 8 members of this series of compounds, confirming our laboratory's previous observations of weak mutagenic response at high dose levels for cis-1,2-disubstituted epoxides. While mutagenicity decreased with expanding ring size, inhibition of bacterial growth increased for increases in ring size. Toxicity accompanying the required high doses for the demonstration of mutagenicity for these compounds prevented the establishment of meaningful dose-response ranges for the remaining epoxides tested. The volatility observed with these oxiranes also made dose-response establishment difficult but was countered by the use of petri dish sealing bands during incubation. Mutagenicity in this series was found to be generally more pronounced in TA1535 while toxicity was detected with greater sensitivity by TA100. The use of the less permeable strains TA92, TA1950 and TA2410, all having normal lipopolysaccharide cell wall coatings, failed to reduce this marked toxicity. The repair test compared results in TA1535 (repair-deficient strain) with TA1975 (repair-proficient strain) and demonstrated that the bacteria were not being killed by damage to DNA since toxicity was not reduced in TA1975.
在不添加肝匀浆组分的情况下,使用艾姆斯沙门氏菌试验研究了12种脂环族环氧化物的致突变性。在该系列化合物的8个成员中检测到碱基对取代诱变活性,证实了我们实验室先前关于顺式1,2 - 二取代环氧化物在高剂量水平下诱变反应较弱的观察结果。虽然诱变活性随环大小的增加而降低,但细菌生长抑制随环大小的增加而增加。这些化合物显示致突变性所需的高剂量所伴随的毒性,使得无法为其余测试的环氧化物确定有意义的剂量 - 反应范围。这些环氧乙烷观察到的挥发性也使得剂量 - 反应的确定变得困难,但在培养过程中使用培养皿密封带可抵消这一影响。发现该系列中的致突变性在TA1535中通常更明显,而TA100对毒性的检测更敏感。使用渗透性较低的菌株TA92、TA1950和TA2410(均具有正常的脂多糖细胞壁涂层)未能降低这种明显的毒性。修复试验比较了TA1535(修复缺陷菌株)和TA1975(修复 proficient菌株)的结果,证明细菌不是因DNA损伤而被杀死,因为TA1975中的毒性并未降低。