Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10768179 | Biochemical and Biophysical Research Communications | 2005 | 8 Pages |
Abstract
Enzymes that effect with ease one of the most difficult chemical reactions, hydroxylation of an unfunctionalized alkyl group, are of particular interest because highly reactive intermediates must be produced. A typical example, the hydroxylation of fatty acids in the Ï position, is now known to occur widely in nature. The catalysts, which can be called “Ï-oxygenases,” also insert molecular oxygen into a variety of other substrates at positions removed from activating functional groups, as in steroids, eicosanoids, and numerous drugs and other xenobiotics. Progress in the characterization of bacterial nonheme-iron enzymes, and plant, bacterial, and mammalian P450 cytochromes that catalyze fatty acid Ï-oxidation, and evidence for multiple functional oxidants are summarized.
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Authors
Minor J. Coon,