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艾姆斯沙门氏菌/微粒体诱变性试验。

The Ames Salmonella/microsome mutagenicity assay.

作者信息

Mortelmans K, Zeiger E

机构信息

Molecular and Genetic Toxicology Program, SRI International, Menlo Park, CA 94025-3493, USA.

出版信息

Mutat Res. 2000 Nov 20;455(1-2):29-60. doi: 10.1016/s0027-5107(00)00064-6.

Abstract

The Ames Salmonella/microsome mutagenicity assay (Salmonella test; Ames test) is a short-term bacterial reverse mutation assay specifically designed to detect a wide range of chemical substances that can produce genetic damage that leads to gene mutations. The test employs several histidine dependent Salmonella strains each carrying different mutations in various genes in the histidine operon. These mutations act as hot spots for mutagens that cause DNA damage via different mechanisms. When the Salmonella tester strains are grown on a minimal media agar plate containing a trace of histidine, only those bacteria that revert to histidine independence (his(+)) are able to form colonies. The number of spontaneously induced revertant colonies per plate is relatively constant. However, when a mutagen is added to the plate, the number of revertant colonies per plate is increased, usually in a dose-related manner. The Ames test is used world-wide as an initial screen to determine the mutagenic potential of new chemicals and drugs. The test is also used for submission of data to regulatory agencies for registration or acceptance of many chemicals, including drugs and biocides. International guidelines have been developed for use by corporations and testing laboratories to ensure uniformity of testing procedures. This review provides historical aspects of how the Ames was developed and detailed procedures for performing the test, including the design and interpretation of results.

摘要

艾姆斯沙门氏菌/微粒体诱变性试验(沙门氏菌试验;艾姆斯试验)是一种短期细菌回复突变试验,专门设计用于检测多种能够产生导致基因突变的遗传损伤的化学物质。该试验采用几种组氨酸依赖型沙门氏菌菌株,每种菌株在组氨酸操纵子的不同基因中携带不同的突变。这些突变作为诱变剂的热点,通过不同机制导致DNA损伤。当沙门氏菌测试菌株在含有微量组氨酸的基本培养基琼脂平板上生长时,只有那些回复为组氨酸非依赖型(his(+))的细菌才能形成菌落。每平板自发诱导的回复菌落数相对恒定。然而,当向平板中加入诱变剂时,每平板的回复菌落数会增加,通常呈剂量相关方式。艾姆斯试验在全球在全球范围内用作初步筛选,以确定新化学物质和药物的诱变潜力。该试验还用于向监管机构提交数据,以注册或批准许多化学物质,包括药物和杀生物剂。已经制定了国际指南供公司和测试实验室使用,以确保测试程序的一致性。本综述提供了艾姆斯试验如何发展的历史背景以及进行该试验的详细程序,包括结果的设计和解释。

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