Sulfinyl radical formation from the reaction of cysteine and glutathione thiyl radicals with molecular oxygen

1987 ◽  
Vol 144 (2) ◽  
pp. 1037-1042 ◽  
Author(s):  
Michael D. Sevilla ◽  
David Becker ◽  
Steven Swarts ◽  
John Herrington
Author(s):  
Jörg Mönig ◽  
Klaus-Dieter Asmus ◽  
Luigi G. Forni ◽  
Robin L. Willson

1988 ◽  
Vol 251 (3) ◽  
pp. 893-899 ◽  
Author(s):  
H Iwahashi ◽  
T Ishii ◽  
R Sugata ◽  
R Kido

Superoxide dismutase (SOD) enhanced the formation of hydroxyl radicals, which were detected by using the e.s.r. spin-trapping technique, in a reaction mixture containing 3-hydroxyanthranilic acid (or p-aminophenol), Fe3+ ions, EDTA and potassium phosphate buffer, pH 7.4. The hydroxyl-radical formation enhanced by SOD was inhibited by catalase and desferrioxamine, and stimulated by EDTA and diethylenetriaminepenta-acetic acid, suggesting that both hydrogen peroxide and iron ions participate in the reaction. The hydroxyl-radical formation enhanced by SOD may be considered to proceed via the following steps. First, 3-hydroxyanthranilic acid is spontaneously auto-oxidized in a process that requires molecular oxygen and yields superoxide anions and anthranilyl radicals. This reaction seems to be reversible. Secondly, the superoxide anions formed in the first step are dismuted by SOD to generate hydrogen peroxide and molecular oxygen, and hence the equilibrium in the first step is displaced in favour of the formation of superoxide anions. Thirdly, hydroxyl radicals are generated from hydrogen peroxide through the Fenton reaction. In this Fenton reaction Fe2+ ions are available since Fe3+ ions are readily reduced by 3-hydroxyanthranilic acid. The superoxide anions do not seem to participate in the reduction of Fe3+ ions, since superoxide anions are rapidly dismuted by SOD present in the reaction mixture.


2009 ◽  
Vol 38 (12) ◽  
pp. 1150-1151 ◽  
Author(s):  
Hiroshi Chishima ◽  
Mitsuo Koshi ◽  
Kenichi Tonokura

2007 ◽  
Vol 1 (1) ◽  
pp. 27-29
Author(s):  
Yuriy Trach ◽  
◽  
Lidiya Bulgakova ◽  
Oksana Makota ◽  
◽  
...  

The initial stages of liquid-phase oxidation of cyclooctene by molecular oxygen in the presence of tert-butyl hydroperoxide were investigated. It was shown that radical formation is the result of bimolecular decomposition of hydroperoxide. The influence of azodiizobutyronitrile on this process was studied. The kinetic parameters of the process were calculated.


1995 ◽  
Vol 36 (45) ◽  
pp. 8197-8200 ◽  
Author(s):  
Evelyne Banchereau ◽  
Sylvie Lacombe ◽  
Jean Ollivier

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