- Source: Oxygen rebound mechanism
In biochemistry, the oxygen rebound mechanism is the pathway for hydroxylation of organic compounds by iron-containing oxygenases. Many enzymes effect the hydroxylation of hydrocarbons as a means for biosynthesis, detoxification, gene regulation, and other functions. These enzymes often utilize Fe-O centers that convert C-H bonds into C-OH groups. The oxygen rebound mechanism starts with abstraction of H from the hydrocarbon, giving an organic radical and an iron hydroxide. In the rebound step, the organic radical attacks the Fe-OH center to give an alcohol group, which is bound to Fe as a ligand. Dissociation of the alcohol from the metal allows the cycle to start anew. This mechanistic scenario is an alternative to the direct insertion of an O center into a C-H bond. The pathway is an example of C-H activation.
Three main classes of these enzymes are cytochrome P450, alpha-ketoglutarate-dependent hydroxylases, and nonheme-diiron hydroxylases.
References
Kata Kunci Pencarian:
- Oxygen rebound mechanism
- Cytochrome P450
- John T. Groves
- Hydroxylation
- Transition metal oxo complex
- Rebound exercise
- Carbon–hydrogen bond activation
- Non-innocent ligand
- Alpha-ketoglutarate-dependent hydroxylases
- Cytochrome P450 aromatic O-demethylase
