Literature DB >> 3900709

Evaluation of the new system (umu-test) for the detection of environmental mutagens and carcinogens.

Y Oda, S Nakamura, I Oki, T Kato, H Shinagawa.   

Abstract

The umu operon in Escherichia coli is responsible for chemical and radiation mutagenesis, and the expression of the operon itself is inducible by these DNA-damaging agents. The principle of the umu-test is based on the ability of the DNA-damaging agents, most of which are potential carcinogens, to induce the umu operon. A plasmid (pSK1002) carrying a fused gene umuC'-'lacZ was introduced into Salmonella typhimurium TA1535. The strain TA1535/pSK1002 enabled us to monitor the levels of umu operon expression by measuring the beta-galactosidase activity in the cells produced by the fusion gene. Using this strain, a simple, inexpensive, and sensitive system, the umu-test, for the screening of environmental mutagens and carcinogens was developed. 38 chemicals with different structures and modes of action, including 31 known animal carcinogens, were examined by the test to evaluate the system. The threshold sensitivity of the umu-test was approximately equal to that of the Ames test for chemicals genotoxic in both tests. By the umu-test, using the single tester strain, we detect many types of DNA-damaging agents for which the Ames test requires several tester strains. Furthermore, the umu-test provides a potential practical advantage for the screening of various environmental samples containing amino acids and nutrients such as urine, serum and foods.

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Year:  1985        PMID: 3900709     DOI: 10.1016/0165-1161(85)90062-7

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  62 in total

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2.  Construction of a ColD cda promoter-based SOS-green fluorescent protein whole-cell biosensor with higher sensitivity toward genotoxic compounds than constructs based on recA, umuDC, or sulA promoters.

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4.  Immobilization as a technical possibility for long-term storage of bacterial biosensors.

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5.  Deletion of MAG1 and MRE11 enhances the sensitivity of the Saccharomyces cerevisiae HUG1P-GFP promoter-reporter construct to genotoxicity.

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Journal:  Biosens Bioelectron       Date:  2008-07-01       Impact factor: 10.618

6.  Daily lifestyles and anti-mutagenicity of saliva.

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7.  The unique correlation between anti-mutagenicity of human saliva and change in body weight.

Authors:  M Toda; K Morimoto; S Nakamura; T Umeda; S Nakaji; K Sugawara
Journal:  Environ Health Prev Med       Date:  2001-07       Impact factor: 3.674

8.  A further note on the sampling device for the anti-mutagenicity of saliva.

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9.  Assessment of Damage to Nucleic Acids and Repair Machinery in Salmonella typhimurium Exposed to Chlorine.

Authors:  M H Phe; M Hajj Chehade; H Guilloteau; C Merlin; J C Block
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10.  Novel application of low pH-dependent fluorescent dyes to examine colitis.

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