Title of article
New Synthetic Models of Cytochrome P450: How Different Are They from the Natural Species?
Author/Authors
Woggon، Wolf-D. نويسنده , , Kozuch، Sebastian نويسنده , , Leifels، Tycho نويسنده , , Meyer، Dominik نويسنده , , Sbaragli، Laura نويسنده , , Shaik، Sason نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
-674
From page
675
To page
0
Abstract
Soluble and matrix-bound P450 enzyme models have been synthesized carrying a SO3- ligand coordinating to iron. These complexes display features very similar to cofactors of enzymes such as P450cam with respect to electrochemistry and UV/Vis spectroscopy. Further they catalyze epoxidation reactions with turnover numbers up to 1800. DFT calculations revealed that the coordination of SO3- to Fe(III) produces an active species that displays allylic hydroxylation and epoxidation reactivity patterns that are nearly indistinguishable from those calculated for the natural active species of the enzyme cytochrome P450.
Keywords
enzyme models , heme-thiolate proteins , iron porphyrins , DFT calculations
Journal title
Synlett
Serial Year
2005
Journal title
Synlett
Record number
110653
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