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Electron-spin-resonance evidence for enzymic reduction of oxygen to a free radical, the superoxide ion

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Knowles, P F, Gibson, J. F., Pick, F. M., Bray, R C·1969·Biochemical Journal

Abstract

1. An electron-spin-resonance signal with g∥2·08 and g⊥2·00 is observed by the rapid-freezing technique during the oxidation of substrates by molecular oxygen catalysed by xanthine oxidase at pH10. 2. The intensity of this signal is shown to depend on oxygen rather than on enzyme concentration, indicating that it is due to an oxygen free radical and not to the enzyme. 3. The same species is shown to be produced in the reaction at pH10 between hydrogen peroxide and periodate ions. Studies with this system have facilitated comparison of the properties of the oxygen radical with data in the literature on the products of pulse radiolysis of oxygenated water over a wide pH range. 4. It is concluded that the species observed is the superoxide ion, O2−, and that the stability of this ion is greatly increased in alkaline solution. A mechanism explaining the alkaline stability is proposed. 5. The importance of O2− in the enzymic reaction is discussed.

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Metadata

Authors
Knowles, P. F., Gibson, J. F., Pick, F. M., & Bray, R. C.
Venue
Biochemical Journal
Published
1969-01-01
Volume
111
Issue
1
Pages
53-58
ISSN
0306-3283 (ISSN-L)
OpenAlex
W2270686920
Cited by
244
References
0
FWCI
20.45
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Electron-spin-resonance evidence for enzymic reduction of oxygen to a free radical, the superoxide ion. https://app.cochat.ai/papers/10.1042/bj1110053
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Knowles, P. F., Gibson, J. F., Pick, F. M., & Bray, R. C. (1969). Electron-spin-resonance evidence for enzymic reduction of oxygen to a free radical, the superoxide ion. Biochemical Journal. https://doi.org/10.1042/bj1110053

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