Abstract

Umu test have been widely used to predict the detection and assessment of DNA- damaging chemicals in environmental genotoxicity field for three decades. This test system is more useful with respect to simplicity, sensitivity, rapidity, and reproducibility. A review of the literature on the development of the umu test is presented in this article. The contents of this article are included a description of numerous data using the umu test. This test have been fully evaluated and used in many directions. Different genetically engineered umu systems introducing bacterial and rat or human drug metabolizing enzymes into the umu tester strains, have been successfully established and are considered as useful tools for genotoxicity assays to study the mechanisms of biotransformation in chemical carcinogenesis. Actually, we developed that two types of bacterial metabolizing enzymes and 4 types of rat and human metabolizing enzyme DNAs are expressed in these strains such as nitroreductase and O-acetyltransferase, cytochrome P450, N-acetyltransferases, sulfotransferases, and glutathione S-transferases, respectively. Due to increasing numbers of minute environmental samples and new pharmaceuticals, a high-throughput umu test system using Salmonella typhimurium TA1535/pSK1002, NM2009, and NM3009 strains provides a useful for these genotoxicity screening. I also briefly describe the first attempts to incorporate such umu tester strain into photo-genotoxicity test.

Highlights

  • Since 1970, a variety of bacterial genotoxicity assays have been developed using Escherichia coli and Salmonella enterica serovar Typhimurium (S. typhimurium) tester strains

  • The results indicated that P450 1B1 is involved in the bioactivation of various procarcinogenic chemicals to DNAdamaging products in the umu assay using S. typhimurium NM2009

  • The results revealed that three selected polycyclic aromatic hydrocarbons (PAHs) (5-methylchrysene, B[a]P, and B[a]A) inhibited metabolic activation of 5methylchrysene-1,2-diol, (+/−)-B[a]P-7,8-diol, dibenzo[a,l] pyrene-11,12-diol, and MeIQ to genotoxic metabolites catalyzed by P450 1A1, 1A2, and 1B1 in S. typhimurium NM2009 [47]

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Summary

Introduction

Since 1970, a variety of bacterial genotoxicity assays have been developed using Escherichia coli and Salmonella enterica serovar Typhimurium (S. typhimurium) tester strains. Development of tester strains that can detect nitroarenes and arylamines with high sensitivity Since bacteria such as E. coli and S. typhimurium using genotoxicity assays have little capacity for bioactivation of chemicals, the assays are indispensable to the use of exogenous mammalian enzyme systems such as S9 fraction.

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