Bowden J P, Chung K T, Andrews A W
J Natl Cancer Inst. 1976 Oct;57(4):921-4. doi: 10.1093/jnci/57.4.921.
The catabolism of tryptophan by rat intestinal microflora was studied for the production of mutagenic metabolites that might be involved in the etiology of colon cancer. Various tryptophan metabolites were assayed for mutagenic and comutagenic activity in the Ames bacterial test system. These included metabolites that were identified by thin-layer chromatography in cultures of rat fecal bacteria, other compounds structurally related to tryptophan, whole unfractionated mixed fecal bacteria culture filtrates, and concentrated solvent extracts. A total of 27 materials were tested with 5 Salmonella strains in the mutagenesis assay. Most substances were inactive, and only one compound, o-aminoacetophenone, which was unlikely to be produced in the intestine, showed weak comutagenic activity. Our results did not support the hypothesis that tryptophan metabolites produced by intestinal microflora are major etiologic factors in cancer of the colon.
研究了大鼠肠道微生物群对色氨酸的分解代谢,以确定是否会产生可能与结肠癌病因有关的诱变代谢产物。在艾姆斯细菌检测系统中,对各种色氨酸代谢产物的诱变和共诱变活性进行了测定。这些代谢产物包括在大鼠粪便细菌培养物中通过薄层色谱法鉴定的代谢产物、其他与色氨酸结构相关的化合物、未经分离的混合粪便细菌培养滤液以及浓缩溶剂提取物。在诱变试验中,用5种沙门氏菌菌株对总共27种物质进行了测试。大多数物质无活性,只有一种不太可能在肠道中产生的化合物邻氨基苯乙酮显示出微弱的共诱变活性。我们的结果不支持肠道微生物群产生的色氨酸代谢产物是结肠癌主要病因的假说。