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黄曲霉毒素B1因羟基化导致的致突变性降低:对五株鼠伤寒沙门氏菌测试菌株的观察

The reduced mutagenicity of aflatoxin B1 due to hydroxylation: observations on five Salmonella typhimurium tester strains.

作者信息

Uwaifo A O, Bababunmi E A

出版信息

Cancer Lett. 1979 Aug;7(4):221-5. doi: 10.1016/s0304-3835(79)80084-1.

Abstract

The mutagenicity of aflatoxin M1 relative to that of aflatoxin B1, the parent compound, was studied in 5 Ames' tester strains of Salmonella typhimurium (TA 98, TA 100, TA 1535, TA 1537, TA 1538). Aflatoxins B1 and M1 are both highly mutagenic in microsome-mediated system in TA 100. The prediction of the relative carcinogenicity of aflatoxin M1 to aflatoxin B1 posed by the mutation of TA 100 is probably more authentic than by TA 98.

摘要

在5种鼠伤寒沙门氏菌(TA 98、TA 100、TA 1535、TA 1537、TA 1538)的艾姆斯试验菌株中,研究了黄曲霉毒素M1相对于其母体化合物黄曲霉毒素B1的致突变性。黄曲霉毒素B1和M1在TA 100的微粒体介导系统中均具有高度致突变性。由TA 100的突变所预测的黄曲霉毒素M1相对于黄曲霉毒素B1的相对致癌性可能比TA 98的预测更可靠。

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