Abstract
The reliable detection of a superoxide anion radical O-2(.-) - is complicated by its spontaneous dismutation reaction to H2O2 at acidic pHs. To simultaneously detect both O-2(.-) and H2O2 produced in the course of its spontaneous dismutation, an electrochemical two-electrode system based on cytochrome c (cyt c) and recombinant horseradish peroxidase (rHRP) was applied. Therewith, a limited applicability of the cyt c system for the reliable monitoring of O-2(.-) in acidic and neutral solutions was shown. It was demonstrated that both the reaction of O-2(.-) dismutation to H2O2 and the reaction between the formed H2O2 and O-2(.-) chemically decrease the amount of the initially present O-2(.-) decreasing the sensitivity and reliability of the electrochemical detection at acidic pH. However, by appropriately varying solution pH, the concentration of O-2(.-) - initially injected in the system can be estimated from the analysis of calibration curves for H2O2 obtained with highly sensitive rHRP-modified electrode system at pH 6.0 and 7.0. (C) 2004 Elsevier B.V. All rights reserved.
Original language | English |
---|---|
Pages (from-to) | 277-280 |
Journal | Bioelectrochemistry |
Volume | 63 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 2004 |
Bibliographical note
The information about affiliations in this record was updated in December 2015.The record was previously connected to the following departments: Biochemistry and Structural Biology (S) (000006142), Analytical Chemistry (S/LTH) (011001004)
Subject classification (UKÄ)
- Analytical Chemistry
- Biological Sciences
Free keywords
- Bi-electrode system
- Recombinant horseradish peroxidase
- Cytochrome c
- Hydrogen peroxide
- Superoxide radical