• 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