Abstract
Steady-state and single-turnover kinetics for the oxidation of the N- substituted phenothiazines (PTs) and phenoxazines (POs) catalyzed by fungal Coprinus cinereus peroxidase and Polyporus pinsitus laccase were investigated at pH 4-10. In the case of peroxidase, an apparent bimolecular rate constant (expressed as k(cat)/K(m)) varied from 1 x 107 M-1 s-1 to 2.6 x 108 M- 1 s-1 at pH 7.0. The constants for PO oxidation were higher in comparison to PT. pH dependence revealed two or three ionizable groups with pK(a) values of 4.9-5.7 and 7.7-9.7 that significantly affected the activity of peroxidase. Single-turnover experiments showed that the limiting step of PT oxidation was reduction of compound II and second-order rate constants were obtained which were consistent with the constants at steady-state conditions. Laccase-catalyzed PT and PO oxidation rates were lower; apparent bimolecular rate constants varied from 1.8 x 105 M- 1 s-1 to 2.0 x 107 M-1 s-1 at pH 5.3. PO constants were higher in comparison to PT, as was the case with peroxidase. The dependence of the apparent bimolecular constants of compound II or copper type 1 reduction, in the case of peroxidase or laccase, respectively, was analyzed in the framework of the Marcus outer-sphere electron-transfer theory. Peroxidase-catalyzed reactions with PT, as well as PO, fitted the same hyperbolic dependence with a maximal oxidation rate of 1.6 x 108 M-1 s-1 and a reorganization energy of 0.30 eV. The respective parameters for laccase were 5.0 x 107 M-1 s-1 and 0.29 eV.
Original language | English (US) |
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Pages (from-to) | 333-340 |
Number of pages | 8 |
Journal | Journal of Biological Inorganic Chemistry |
Volume | 5 |
Issue number | 3 |
DOIs | |
State | Published - Jun 2000 |
Keywords
- Laccase
- Peroxidase
- Phenothiazine
- Phenoxazine
- Rate constant
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry