Selective oxidation of aromatic sulfide catalyzed by an artificial metalloenzyme: new activity of hemozymes

Org Biomol Chem. 2009 Aug 21;7(16):3208-11. doi: 10.1039/b907534h. Epub 2009 Jun 23.

Abstract

Two new artificial hemoproteins or "hemozymes", obtained by non covalent insertion of Fe(III)-meso-tetra-p-carboxy- and -p-sulfonato-phenylporphyrin into xylanase A from Streptomyces lividans, were characterized by UV-visible spectroscopy and molecular modeling studies, and were found to catalyze the chemo- and stereoselective oxidation of thioanisole into the S sulfoxide, the best yield (85 +/- 4%) and enantiomeric excess (40% +/- 3%) being obtained with Fe(III)-meso-tetra-p-carboxyphenylporphyrin-Xln10A as catalyst in the presence of imidazole as co-catalyst.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Metalloproteins / chemistry*
  • Molecular Structure
  • Oxidation-Reduction
  • Oxygen / chemistry*
  • Sulfides / chemistry*
  • Sulfoxides / chemistry

Substances

  • Metalloproteins
  • Sulfides
  • Sulfoxides
  • methylphenylsulfide
  • Oxygen