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基于黄嘌呤-黄嘌呤氧化酶还原3'-[1-(苯氨基)-羰基]-3,4-四氮唑]-双(4-甲氧基-6-硝基)苯磺酸水合物(一种四氮唑盐)的超氧化物歧化酶分光光度测定法

Spectrophotometric assay for superoxide dismutase based on tetrazolium salt 3'--1--(phenylamino)-carbonyl--3, 4-tetrazolium]-bis(4-methoxy-6-nitro)benzenesulfonic acid hydrate reduction by xanthine-xanthine oxidase.

作者信息

Ukeda H, Maeda S, Ishii T, Sawamura M

机构信息

Faculty of Agriculture, Kochi University, Monobe B-200, Nankoku, 783, Japan.

出版信息

Anal Biochem. 1997 Sep 5;251(2):206-9. doi: 10.1006/abio.1997.2273.

Abstract

XTT (3'-{1-[(phenylamino)-carbonyl]-3, 4-tetrazolium}bis(4-methoxy-6-nitro)benzenesulfonic acid hydrate) was reduced to a water-soluble product with an absorbance maximum at about 470 nm by superoxide anion generated by xanthine-xanthine oxidase (XO). The rate of XTT reduction was linearly related to XO activity and the reduction was inhibited by superoxide dismutase (SOD). A perfect inhibition of the reduction of XTT by SOD was achieved, suggesting that XTT does not interact with XO. The present XTT-based assay had a higher sensitivity than a conventional nitroblue tetrazolium-based assay by a factor of 2.5 at pH 10.2. This method was applicable to the SOD assay in the pH range 8.0-10.2.

摘要

XTT(3'-{1-[(苯氨基)-羰基]-3,4-四氮唑}双(4-甲氧基-6-硝基)苯磺酸水合物)被黄嘌呤-黄嘌呤氧化酶(XO)产生的超氧阴离子还原为一种在约470nm处有最大吸光度的水溶性产物。XTT的还原速率与XO活性呈线性相关,且该还原反应受到超氧化物歧化酶(SOD)的抑制。SOD对XTT的还原实现了完全抑制,这表明XTT不与XO相互作用。在pH 10.2时,基于XTT的当前检测方法的灵敏度比传统的基于硝基蓝四氮唑的检测方法高2.5倍。该方法适用于pH范围为8.0 - 10.2的SOD检测。

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