Oda Yoshimitsu
Institute of Life and Environmental Sciences, Osaka Shin-Ai College, 6-2-28 Tsurumi, Tsurumi-ku, 538-0053, Japan.
Adv Biochem Eng Biotechnol. 2017;157:97-134. doi: 10.1007/10_2016_4.
During the past 30 years there has been considerable progress in the development of bacterial test systems for use in genotoxicity testing by the stable introduction of expression vectors (cDNAs) coding for xenobiotic-metabolizing enzymes into bacterial cells. The development not only provides insights into the mechanisms of bioactivation of xenobiotic compounds but also evaluates the roles of enzymes involved in metabolic activation or inactivation in chemical carcinogenesis. This review describes recent advances in bacterial genotoxicity assays and their future prospects, with a focus on the development and application of genetically engineering bacterial cells to incorporate some of the enzymatic activities involved in the bio-activation process of xenobiotics. Various genes have been introduced into bacterial umu tester strains encoding enzymes for genotoxic bioactivation, including bacterial nitroreductase and O-acetyltransferase, human cytochrome P450 monooxygenases, rat glutathione S-transferases, and human N-acetyltransferases and sulfotransferases. Their application has provided new tools for genotoxicity assays and for studying the role of biotransformation in chemical carcinogenesis in humans.
在过去30年里,通过将编码异生物质代谢酶的表达载体(cDNA)稳定导入细菌细胞,用于遗传毒性测试的细菌测试系统有了长足的发展。这一发展不仅有助于深入了解异生物质化合物的生物活化机制,还能评估参与化学致癌过程中代谢活化或失活的酶的作用。本文综述了细菌遗传毒性检测的最新进展及其未来前景,重点关注基因工程细菌细胞的开发和应用,以纳入一些参与异生物质生物活化过程的酶活性。各种基因已被导入细菌umu测试菌株,这些菌株编码用于遗传毒性生物活化的酶,包括细菌硝基还原酶和O - 乙酰转移酶、人细胞色素P450单加氧酶、大鼠谷胱甘肽S - 转移酶以及人N - 乙酰转移酶和磺基转移酶。它们的应用为遗传毒性检测以及研究生物转化在人类化学致癌中的作用提供了新工具。