FORMATION OF DNA ADDUCTS INVITRO AND IN SALMONELLA-TYPHIMURIUM UPON METABOLIC REDUCTION OF THE ENVIRONMENTAL MUTAGEN 1-NITROPYRENE

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  • 1 January 1983
    • journal article
    • research article
    • Vol. 43  (5) , 2052-2058
Abstract
The polycyclic nitroaromatic hydrocarbon 1-nitropyrene is an environmental pollutant, a potent bacterial mutagen and a carcinogen. Xanthine oxidase, a mammalian nitroreductase, catalyzed the in vitro metabolic activation of this compound to DNA-bound adducts. Maximum adduct formation occurred at pH 5.5-6.0 and was increased by the addition of catalase to the incubation medium. DNA binding from 1-nitropyrene was inhibited by hydrogen peroxide, L-ascorbate and glutathione. Enzymatic hydrolysis of the modified DNA and subsequent analysis by high-pressure liquid chromatography indicated the presence of 1 major and 2 minor adducts. The major adduct was characterized by mass spectrometry and NMR spectroscopy as N-(deoxyguanosin-8-yl)-1-aminopyrene. The minor adducts appear to be decomposition products of the major adduct. When S. typhimurium TA1538 was incubated with 1-nitropyrene, a strong correlation was found between the extent of DNA binding and the frequency of induced histidine reversions. Analysis of the bacterial DNA indicated one major adduct which had chromatographic properties and pKa identical to those of N-(deoxyguanosin-8-yl)-1-aminopyrene. N-Hydroxy-1-aminopyrene is probably the mutagenic and DNA-binding species formed during the metabolic reduction of 1-nitropyrene.