Detection of free radicals generated from hydrogen peroxide, gallic acid and haemoprotein chemiluminescence system by electron spin resonance spectroscopy

被引:0
|
作者
Kawane, M
Iida, T
Yoshiki, Y
Okubo, K
Tsunakawa, M
机构
[1] Tohoku Univ, Dept Environm Bioremediat, Grad Sch Agr Sci, Aoba Ku, Sendai, Miyagi 9818555, Japan
[2] Takano Foods Co Ltd, Higashiibaraki, Ibaraki 3113411, Japan
关键词
chemiluminescence; haemoprotein; hydrogen peroxide; free radical; electron spin resonance;
D O I
10.1002/(SICI)1522-7243(199911/12)14:6<321::AID-BIO568>3.0.CO;2-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Low-level chemiluminescence is produced in a hydrogen peroxide (H(2)O(2))/gallic acid/haemoprotein system with single broad peaks around 520 nm, regardless of the biological role of the haemoprotein. The free haem iron systems (haemin and haematin systems) gave a higher photon intensity (1.5 x 10(4) and 2.0 x 10(4) cpa) than that of the H(2)O(2)/gallic acid/haematoporphyrin system. These results indicated that haem iron plays a significant role in the photon emission of haemoprotein systems. A free radical with a g value of 2.0058 was detected through a direct electron spin resonance (ESR) method. The photon intensity of the H(2)O(2)/gallic acid/ haemoprotein system decreased in the order: HRP > cytochrome c > myoglobin > haemoglobin, and this corresponded to the decrease in radical intensity. These results indicated that the formation of the free radical with a g value of 2.0058 may be the key step for chemiluminescence in the H(2)O(2)/gallic acid/haemoprotein system. A quarrel line similar to DMPO-OH adducts and uncomplexed free radicals (g = 2.0058) was detected using the ESR spin-trapping method in the H(2)O(2)/gallic acid/cytochrome c system. Copyright (C) 1999 John Wiley & Sons, Ltd.
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页码:321 / 325
页数:5
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