Wilkins T D, Lederman M, Van Tassell R L, Kingston D G, Henion J
Am J Clin Nutr. 1980 Nov;33(11 Suppl):2513-20. doi: 10.1093/ajcn/33.11.2513.
Mutagens detectable with the Ames assay have been found in the feces of apparently healthy individuals and the incidence of this mutagenic activity was found to be greater in a population at high risk for colon cancer than in a population at low risk. A compound accounting for the mutagenic activity has been isolated by high performance liquid chromatography. Two closely related forms which behave identically chemically could be resolved. The compound was active on Salmonella typhimurium TA98 and TA100, had a characteristic ultraviolet absorption spectrum with maxima at about 320, 340, and 365 nm, fluoresced green in long wavelength ultraviolet light, and had the same mobility on the thin-layer chromatography as the mutagenic activity in a direct ether extract of feces. The compound was unstable in air but could be stabilized in the presence of butylated hydroxytoluene. Upon oxidation the compound lost its mutagenicity and its ultraviolet absorption spectrum underwent a blue shift so that the absorption maxima were at 295, 310, and 325 nm. Determination of the structure of the mutagen has been difficult since the compound was not volatile and production of a volatile derivative has not been successful. On thin-layer chromatography plates the compound reacted with reagents that detect chlorinated compounds. By thermal energy analysis it did not appear to contain a nitroso group. The compound increased in concentration upon anaerobic incubation of feces at 37 C and this increase was prevented by cold, air, and antimicrobial agents. This suggests to us that the fecal flora produces the compound.
在表面健康个体的粪便中发现了可用艾姆斯试验检测到的诱变剂,并且发现这种诱变活性在结肠癌高风险人群中的发生率高于低风险人群。通过高效液相色谱法已分离出一种导致诱变活性的化合物。可以分辨出两种化学行为相同的紧密相关形式。该化合物对鼠伤寒沙门氏菌TA98和TA100有活性,具有特征性的紫外吸收光谱,最大吸收峰在约320、340和365纳米处,在长波紫外线下发出绿色荧光,并且在薄层色谱上的迁移率与粪便直接乙醚提取物中的诱变活性相同。该化合物在空气中不稳定,但在丁基化羟基甲苯存在下可稳定。氧化后,该化合物失去其诱变活性,其紫外吸收光谱发生蓝移,使得吸收最大值在295、310和325纳米处。由于该化合物不挥发且挥发性衍生物的制备未成功,因此确定诱变剂的结构一直很困难。在薄层色谱板上,该化合物与检测氯化化合物的试剂发生反应。通过热能分析,它似乎不含有亚硝基。在37℃下粪便厌氧培养时,该化合物的浓度增加,而冷、空气和抗菌剂可阻止这种增加。这向我们表明粪便菌群产生了该化合物。