Science · 1982 · 51 citations · 47 references
Life SciencesBiochemistryMicrobiologyBiocatalysisEnzymologyMicrobial MetabolismCatalytic MechanismsEnzymatic CatalysisEnzyme InhibitionEnzyme KineticsDna Binding SpecificityEpoxide Hydrolase ActivityEpoxide HydrolasesEpoxide Metabolites
The mutagenicity of r-8,t-9-dihydroxy-t-10, 11-oxy-8,9,10,11-tetrahydrobenz[a]anthracene (BA-8,9-diol 10, 11-oxide) toward Salmonella typhimurium TA 100 is not decreased by the presence of large amounts of highly purified microsomal or cytosolic epoxide hydrolase. However, highly purified dihydrodiol dehydrogenase inactivates this diol epoxide, which is a major DNA-binding metabolite of benz[a]anthracene. The K-region epoxide, benz[a]anthracene 5,6-oxide (BA 5,6-oxide) is efficiently inactivated by microsomal epoxide hydrolase, is much less readily inactivated by cytosolic epoxide hydrolase, and is not inactivated by dihydrodiol dehydrogenase. This inactivation of a diol epoxide by dihydrodiol dehydrogenase points to a new significance of this enzyme and a new level of control for diol epoxides.
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Metabolic activation of benzo(a)pyrene proceeds by a diol-epoxide
Peter Sims, P.L. Grover, Alan Swaisland et al. · Nature · 1974 · 1.1K citations
Hepatic epoxide hydrase. Structure-activity relations for substrates and inhibitors
Franz Oesch, Nikolaus Kaubisch, D. M. JERINA et al. · Biochemistry · 1971 · 318 citations