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人类肠道微生物群对偶氮染料代谢的毒理学意义。

Toxicological significance of azo dye metabolism by human intestinal microbiota.

作者信息

Feng Jinhui, Cerniglia Carl E, Chen Huizhong

机构信息

Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR 72079-9502, USA.

出版信息

Front Biosci (Elite Ed). 2012 Jan 1;4(2):568-86. doi: 10.2741/e400.

Abstract

Approximately 0.7 million tons of azo dyes are synthesized each year. Azo dyes are composed of one or more R₁-N=N-R₂ linkages. Studies have shown that both mammalian and microbial azoreductases cleave the azo bonds of the dyes to form compounds that are potentially genotoxic. The human gastrointestinal tract harbors a diverse microbiota comprised of at least several thousand species. Both water-soluble and water-insoluble azo dyes can be reduced by intestinal bacteria. Some of the metabolites produced by intestinal microbiota have been shown to be carcinogenic to humans although the parent azo dyes may not be classified as being carcinogenic. Azoreductase activity is commonly found in intestinal bacteria. Three types of azoreductases have been characterized in bacteria. They are flavin dependent NADH preferred azoreductase, flavin dependent NADPH preferred azoreductase, and flavin free NADPH preferred azoreductase. This review highlights how azo dyes are metabolized by intestinal bacteria, mechanisms of azo reduction, and the potential contribution in the carcinogenesis/mutagenesis of the reduction of the azo dyes by intestinal microbiota.

摘要

每年大约合成70万吨偶氮染料。偶氮染料由一个或多个R₁-N=N-R₂键组成。研究表明,哺乳动物和微生物的偶氮还原酶都会裂解染料的偶氮键,形成具有潜在遗传毒性的化合物。人类胃肠道中存在着由至少几千种物种组成的多样化微生物群。水溶性和水不溶性偶氮染料都可被肠道细菌还原。尽管母体偶氮染料可能未被归类为致癌物,但肠道微生物群产生的一些代谢产物已被证明对人类具有致癌性。偶氮还原酶活性常见于肠道细菌中。细菌中已鉴定出三种类型的偶氮还原酶。它们分别是黄素依赖性NADH偏好的偶氮还原酶、黄素依赖性NADPH偏好的偶氮还原酶和无黄素NADPH偏好的偶氮还原酶。本综述重点介绍了偶氮染料如何被肠道细菌代谢、偶氮还原的机制,以及肠道微生物群对偶氮染料还原在致癌作用/诱变作用中的潜在贡献。

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