Literature DB >> 3985960

Spectra of chloroperoxidase compounds II and III.

R Nakajima, I Yamazaki, B W Griffin.   

Abstract

Chloroperoxidase was present as Compound II during the peroxidatic oxidation of ascorbic acid. Compound III (oxy-form) was formed when excess hydrogen peroxide was added to Compound II. By decreasing the temperature it was possible to measure the spectra of Compounds II and III in the Soret and visible regions. Each spectrum was found to resemble that of the corresponding form of lactoperoxidase. Under the experimental conditions, chloroperoxidase Compound III was apparently converted to Compound II in parallel with the decomposition of hydrogen peroxide and finally to the ferric enzyme.

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Year:  1985        PMID: 3985960     DOI: 10.1016/0006-291x(85)91635-3

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  6 in total

1.  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

2.  Structure and quantum chemical characterization of chloroperoxidase compound 0, a common reaction intermediate of diverse heme enzymes.

Authors:  Karin Kühnel; Etienne Derat; James Terner; Sason Shaik; Ilme Schlichting
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-26       Impact factor: 11.205

3.  Superoxide modulates the activity of myeloperoxidase and optimizes the production of hypochlorous acid.

Authors:  A J Kettle; C C Winterbourn
Journal:  Biochem J       Date:  1988-06-01       Impact factor: 3.857

4.  Dioxygen activation and bond cleavage by mixed-valence cytochrome c oxidase.

Authors:  D A Proshlyakov; M A Pressler; G T Babcock
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-07       Impact factor: 11.205

5.  Interactions of the neurotoxic amine 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine with monoamine oxidases.

Authors:  T P Singer; J I Salach; N Castagnoli; A Trevor
Journal:  Biochem J       Date:  1986-05-01       Impact factor: 3.857

6.  A novel intermediate in the reaction of seleno CYP119 with m-chloroperbenzoic acid.

Authors:  Santhosh Sivaramakrishnan; Hugues Ouellet; Jing Du; Kirsty J McLean; Katalin F Medzihradszky; John H Dawson; Andrew W Munro; Paul R Ortiz de Montellano
Journal:  Biochemistry       Date:  2011-03-22       Impact factor: 3.162

  6 in total

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