Literature DB >> 15760172

Formation of compound I by photo-oxidation of compound II.

Rui Zhang1, R Esala P Chandrasena, Enrique Martinez, John H Horner, Martin Newcomb.   

Abstract

[reaction: see text] Compound I is the heme-iron(IV)-oxo porphyrin radical cation formed in peroxidase and catalase enzymes by reaction with hydrogen peroxide. As an alternative to chemical oxidations of porphyrin-iron(III) species, various compound I species were produced by 355 nm laser flash photolysis photooxidation of the corresponding compound II species, porphyrin-iron(IV)-oxo derivatives. The method is demonstrated by production and kinetic studies of the compound I species from 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin-iron, from horseradish peroxidase, and from wild-type horse skeletal myoglobin.

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Year:  2005        PMID: 15760172     DOI: 10.1021/ol050296j

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  17 in total

1.  Cytochrome p450 compound I.

Authors:  Martin Newcomb; Rui Zhang; R Esala P Chandrasena; James A Halgrimson; John H Horner; Thomas M Makris; Stephen G Sligar
Journal:  J Am Chem Soc       Date:  2006-04-12       Impact factor: 15.419

2.  Low temperature photo-oxidation of chloroperoxidase Compound II.

Authors:  Xinting Yuan; Xin Sheng; John H Horner; Brian Bennett; Leslie W-M Fung; Martin Newcomb
Journal:  J Inorg Biochem       Date:  2010-07-17       Impact factor: 4.155

3.  Photochemical generation and kinetic studies of a putative porphyrin-ruthenium(V)-oxo species.

Authors:  Rui Zhang; Eric Vanover; Weilong Luo; Martin Newcomb
Journal:  Dalton Trans       Date:  2014-06-21       Impact factor: 4.390

4.  Spin scavenging analysis of myoglobin protein-centered radicals using stable nitroxide radicals: characterization of oxoammonium cation-induced modifications.

Authors:  Olivier M Lardinois; David A Maltby; Katalin F Medzihradszky; Paul R Ortiz de Montellano; Kenneth B Tomer; Ronald P Mason; Leesa J Deterding
Journal:  Chem Res Toxicol       Date:  2009-06       Impact factor: 3.739

5.  Kinetic isotope effects in hydroxylation reactions effected by cytochrome P450 compounds I implicate multiple electrophilic oxidants for P450-catalyzed oxidations.

Authors:  Xin Sheng; Haoming Zhang; Paul F Hollenberg; Martin Newcomb
Journal:  Biochemistry       Date:  2009-02-24       Impact factor: 3.162

6.  Spectra and kinetic studies of the compound I derivative of cytochrome P450 119.

Authors:  Xin Sheng; John H Horner; Martin Newcomb
Journal:  J Am Chem Soc       Date:  2008-09-13       Impact factor: 15.419

7.  Photochemical production of a highly reactive porphyrin-iron-oxo species.

Authors:  Zhengzheng Pan; Rui Zhang; Leslie W-M Fung; Martin Newcomb
Journal:  Inorg Chem       Date:  2007-02-07       Impact factor: 5.165

Review 8.  Hydrocarbon hydroxylation by cytochrome P450 enzymes.

Authors:  Paul R Ortiz de Montellano
Journal:  Chem Rev       Date:  2010-02-10       Impact factor: 60.622

Review 9.  Laser flash photolysis generation of high-valent transition metal-oxo species: insights from kinetic studies in real time.

Authors:  Rui Zhang; Martin Newcomb
Journal:  Acc Chem Res       Date:  2008-02-16       Impact factor: 22.384

10.  Kinetics and activation parameters for oxidations of styrene by Compounds I from the cytochrome P450(BM-3) (CYP102A1) heme domain and from CYP119.

Authors:  Xinting Yuan; Qin Wang; John H Horner; Xin Sheng; Martin Newcomb
Journal:  Biochemistry       Date:  2009-09-29       Impact factor: 3.162

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