Expanding the substrate scope and reactivity of cytochrome P450 OleT.

[1]  H. Sugimoto,et al.  A substrate-binding-state mimic of H2O2-dependent cytochrome P450 produced by one-point mutagenesis and peroxygenation of non-native substrates , 2016 .

[2]  T. Makris,et al.  Mixed regiospecificity compromises alkene synthesis by a cytochrome P450 peroxygenase from Methylobacterium populi. , 2016, Journal of inorganic biochemistry.

[3]  O. Shoji,et al.  Acetate anion-triggered peroxygenation of non-native substrates by wild-type cytochrome P450s. , 2015, Dalton transactions.

[4]  A. Dennig,et al.  Oxidative Decarboxylation of Short-Chain Fatty Acids to 1-Alkenes. , 2015, Angewandte Chemie.

[5]  Job L Grant,et al.  Decarboxylation of fatty acids to terminal alkenes by cytochrome P450 compound I. , 2015, Journal of the American Chemical Society.

[6]  J. Groves,et al.  Heme-thiolate ferryl of aromatic peroxygenase is basic and reactive , 2015, Proceedings of the National Academy of Sciences.

[7]  D. Bauer,et al.  Photobiocatalytic decarboxylation for olefin synthesis. , 2015, Chemical communications.

[8]  Andrew W. Munro,et al.  Structure and Biochemical Properties of the Alkene Producing Cytochrome P450 OleTJE (CYP152L1) from the Jeotgalicoccus sp. 8456 Bacterium* , 2014, The Journal of Biological Chemistry.

[9]  K. Piontek,et al.  Structural Basis of Substrate Conversion in a New Aromatic Peroxygenase , 2013, The Journal of Biological Chemistry.

[10]  N. Nakamura,et al.  Spectroscopic characterization of the acid–alkaline transition of a thermophilic cytochrome P450 , 2013, FEBS letters.

[11]  J. Groves,et al.  Detection and kinetic characterization of a highly reactive heme-thiolate peroxygenase compound I. , 2012, Journal of the American Chemical Society.

[12]  R. Fasan Tuning P450 Enzymes as Oxidation Catalysts , 2012 .

[13]  Y. Nguyen,et al.  Light-initiated hydroxylation of lauric acid using hybrid P450 BM3 enzymes. , 2011, Chemical communications.

[14]  G. Grogan Cytochromes P450: exploiting diversity and enabling application as biocatalysts. , 2011, Current opinion in chemical biology.

[15]  Andreas Schirmer,et al.  Terminal Olefin (1-Alkene) Biosynthesis by a Novel P450 Fatty Acid Decarboxylase from Jeotgalicoccus Species , 2011, Applied and Environmental Microbiology.

[16]  Michael T. Green,et al.  Cytochrome P450 Compound I: Capture, Characterization, and C-H Bond Activation Kinetics , 2010, Science.

[17]  O. Shoji,et al.  Understanding substrate misrecognition of hydrogen peroxide dependent cytochrome P450 from Bacillus subtilis , 2010, JBIC Journal of Biological Inorganic Chemistry.

[18]  O. Shoji,et al.  Aromatic C–H bond hydroxylation by P450 peroxygenases: a facile colorimetric assay for monooxygenation activities of enzymes based on Russig’s blue formation , 2010, JBIC Journal of Biological Inorganic Chemistry.

[19]  P. R. Montellano Hydrocarbon hydroxylation by cytochrome P450 enzymes. , 2010 .

[20]  M. Hofrichter,et al.  Purification of homogeneous forms of fungal peroxygenase. , 2009, Biotechnology journal.

[21]  Matthias Dietrich,et al.  Cytochrome P450 monooxygenase from Clostridium acetobutylicum: a new alpha-fatty acid hydroxylase. , 2007, Biochemical and biophysical research communications.

[22]  O. Shoji,et al.  Hydrogen peroxide dependent monooxygenations by tricking the substrate recognition of cytochrome P450BSbeta. , 2007, Angewandte Chemie.

[23]  Andrew K. Udit,et al.  Protein-surfactant film voltammetry of wild-type and mutant cytochrome P450 BM3. , 2005, Inorganic chemistry.

[24]  Ilme Schlichting,et al.  Structure and chemistry of cytochrome P450. , 2005, Chemical reviews.

[25]  F. Arnold,et al.  A self-sufficient peroxide-driven hydroxylation biocatalyst. , 2003, Angewandte Chemie.

[26]  Dong-Sun Lee,et al.  Substrate Recognition and Molecular Mechanism of Fatty Acid Hydroxylation by Cytochrome P450 from Bacillus subtilis , 2003, The Journal of Biological Chemistry.

[27]  E. Obayashi,et al.  Enzymatic reaction of hydrogen peroxide-dependent peroxygenase cytochrome P450s: kinetic deuterium isotope effects and analyses by resonance Raman spectroscopy. , 2002, Biochemistry.

[28]  E. Kusunose,et al.  Fatty acid-specific, regiospecific, and stereospecific hydroxylation by cytochrome P450 (CYP152B1) from Sphingomonas paucimobilis: Substrate structure required for α-hydroxylation , 2000, Lipids.

[29]  E. Kusunose,et al.  Further characterization of hydrogen peroxide-dependent fatty acid alpha-hydroxylase from Sphingomonas paucimobilis. , 1998, Journal of biochemistry.

[30]  O. Gotoh,et al.  Molecular Cloning and Expression of Fatty Acid α-Hydroxylase from Sphingomonas paucimobilis * , 1997, The Journal of Biological Chemistry.

[31]  J. Halpert,et al.  Dithionite-supported hydroxylation of palmitic acid by cytochrome P450BM-3. , 1996, Drug metabolism and disposition: the biological fate of chemicals.

[32]  P. Ortiz de Montellano,et al.  Calculated and experimental absolute stereochemistry of the styrene and .beta.-methylstyrene epoxides formed by cytochrome P 450cam , 1992 .

[33]  Ortiz de Montellano,et al.  Cytochrome P-450: Structure, Mechanism, and Biochemistry , 1986 .

[34]  J. Dawson,et al.  Formation of low spin complexes of ferric cytochrome P-450-CAM with anionic ligands. Spin state and ligand affinity comparison to myoglobin. , 1982, The Journal of biological chemistry.

[35]  Vlada B Urlacher,et al.  Cytochrome P450 monooxygenases: an update on perspectives for synthetic application. , 2012, Trends in biotechnology.