Synlett 2005(4): 675-684  
DOI: 10.1055/s-2005-863724
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© Georg Thieme Verlag Stuttgart · New York

New Synthetic Models of Cytochrome P450: How Different Are They from the Natural Species?

Sebastian Kozucha, Tycho Leifelsb, Dominik Meyerb, Laura Sbaraglib, Sason Shaik*a, Wolf-D. Woggon*b
a Department of Organic Chemistry and The Lise Meitner-Minerva Center for Computational Quantum Chemistry, Givat Ram Campus, Jerusalem 91904, Israel
b Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056 Basel, Switzerland
Fax: +41(61)2671102; e-Mail: wolf-d.woggon@unibas.ch;
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Received 3 December 2004
Publikationsdatum:
22. Februar 2005 (online)

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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.