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
Link To Document :
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