Evaluation of the mutagenicity of azo dyes in Salmonella typhimurium: a study of structure—activity relationships
- 1 March 1989
- journal article
- research article
- Published by Oxford University Press (OUP) in Mutagenesis
- Vol. 4 (2) , 115-125
- https://doi.org/10.1093/mutage/4.2.115
Abstract
In order to explore structure—activity relationships, 4, 4'-diaminoazobenzene and four structurally related azo dyes were tested for their ability to induce gene mutations in Salmonella typhimurium strains TA1535, TA100, TA1537, TA1538, and TA98. Only 4, 4'-diaminoazobenzene and 4, 4'-N(β-hydroxyethylamino)azobenzene were found to be active in the two frameshift strains TA1538 and TA98. Further tests were performed in strain TA98, both in the presence and in the absence of Aroclor 1254-induced rat or hamster liver S9 preparations. The amount of S9 used per plate was 50, 100, 150 or 300 μl, which corresponds to 10, 20, 30 or 60% of S9 in S9 mix. 4, 4'-Diaminoazobenzene was found to be mutagenic, and its mutagenicity depended on the percentage of S9 in S9 mix and the type of S9 fraction used. 4, 4'-N-(β-Hydroxyethylamino)azobenzene was less mutagenic than 4, 4'-diaminoazobenzene, indicating a reduction in mutagenicity associated with the β-hydroxyalkyl substituents. The other three azo dyes [4'-methyl-4-N,N-di(β-hydroxyethylamino)azobenzene; 4'-amino-6-methyl-4-N,N-di(β-hydroxyethylamino)azobenzene] were inactive, both in the presence and in the absence of the metabolic activation system. The use of the preincubation test did not alter the observed positive or negative response of these compounds. The importance of this finding is that the non-mutagenicity or decreased mutagenicity of these four compounds is predictable on the basis of their chemical structures. These azo dyes, like the non-mutagenic members of series of monocyclic aromatic amines, contain large substituents on one or both of the amino groups of the parent compound, in this case 4, 4'-diaminoazobenzene. From our earlier data and the experiments discussed in this paper, we conclude that the study of structure-activity relationships can provide useful information for the prediction and interpretation of mutagenic responses.This publication has 8 references indexed in Scilit:
- Structure—activity relationship studies on the mutagenicity of some azo dyes in the Salmonella/microsome assayMutagenesis, 1988
- Comparisons of mutation induction by six monocyclic aromatic amines in salmonella typhimurium tester strains TA97, TA1537, and TA1538Environmental Mutagenesis, 1985
- Mutagenicity of azo dyes following metabolism by different reductive/oxidative systemsEnvironmental Mutagenesis, 1984
- Mutagenicity of structurally related aromatic amines in the Salmonella/mammalian microsome test with various S-9 fractionsFood and Chemical Toxicology, 1983
- Revised methods for the Salmonella mutagenicity testMutation Research/Environmental Mutagenesis and Related Subjects, 1983
- Analysis of a method for testing azo dyes for mutagenic activity in Salmonella typhimurium in the presence of flavin mononucleotide and hamster liver S9Mutation Research/Environmental Mutagenesis and Related Subjects, 1982
- Structure-activity relationships within a series of 2,4-diaminoalkoxybenzene compoundsMutation Research/Genetic Toxicology, 1980
- Structure—activity relationship within a series of m-diaminobenzene derivativesMutation Research/Genetic Toxicology, 1980