Evaluation of Escherichia coli DJ4309 expressing human P450 1A2 in mutagenicity testing of complex food mixtures

Citation
A. Constable et al., Evaluation of Escherichia coli DJ4309 expressing human P450 1A2 in mutagenicity testing of complex food mixtures, MUT RES-GTE, 442(2), 1999, pp. 79-87
Citations number
24
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
ISSN journal
13835718 → ACNP
Volume
442
Issue
2
Year of publication
1999
Pages
79 - 87
Database
ISI
SICI code
1383-5718(19990625)442:2<79:EOECDE>2.0.ZU;2-N
Abstract
Heterocyclic aromatic amines (HAAs) are potent bacterial mutagens and poten tial human carcinogens formed in heat processed proteins. The Ames test (st rain TA98) is a useful mutagenicity test system to screen food products for these compounds. HAAs require activation to their genotoxic forms, and in the Ames test, a rat liver S-9 preparation is normally used. In order to be tter understand the mechanisms of mutagen activation with respect to human metabolism, new bacterial strains containing human cytochrome P450s and oth er metabolic enzymes have recently been developed. We have investigated the capacity of one of these strains, DJ4309 [Josephy et al., Chem. Res. Toxic ol. 11 (1998) 70-74] as a screening tool for mutagens in food products. DJ4 309 expresses the human P450 1A2, human NADPH cytochrome reductase and the bacterial acetyl CoA:arylamine N-acetyltransferase. This strain is as sensi tive as the Ames system to the mutagenic effects of the heterocyclic aromat ic amines 2-amino-3-methylimidazo[4,5-f]quinoline, 2-amino-3,4-dimethylimid azo[4,5-f]quinoline and 2-amino-3,8-dimethylimidazo[4,5 f]quinoxaline, but less sensitive to 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine. However, the mutagenicity of the arylamine 2-aminofluorene is considerably higher i n DJ4309 than in the Ames test system. Meat extracts with a total HAA conte nt ranging from less than 2 ng/g to 20 ng/g are efficiently detected by the Ames TA98 strain with rat liver S-9 activation. DJ4309 is less sensitive, with fewer revertants induced over the same dose range. Unknown compounds p resent in the meat extracts appear to inhibit the activity of the P450 1A2 enzyme in the DJ4309 strain. We have therefore demonstrated that although D J4309 is a useful tool for mechanistic studies in chemical carcinogenesis, the screening of complex food matrices for HAAs by this bacterial strain mu st be conducted with caution. (C) 1999 Elsevier Science B.V. All rights res erved.