一些淡水鱼过氧化氢酶活性的研究——作为潜在的环境污染生物标志物

R. Crețu
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引用次数: 0

摘要

近十年来的研究表明,水污染是一个非常严重的问题,特别是因为水污染的程度对鱼类的生长和繁殖起着关键作用。作为环境污染的生物标志物,抗氧化酶如过氧化氢酶(CAT;EC 1.11.1.6)在防止鱼类组织中重金属的有害影响方面起着至关重要的作用。本研究旨在探讨不同环境条件和污染物对某些水生生物氧化应激的影响。酶法测定CAT(鱼的器官,如肝、肾、鳃、肠和脑,以及这些器官的混合物)按照标准酶法测定方案进行。结果表明,CAT活性降低,pH = 7时酶活性为35.89±1.02µmol H2O2/min/mg蛋白,pH = 12时酶活性为6.59±0.47µmol H2O2/min/mg蛋白。酶活性为38.1±0.3µmol H2O2/min/mg protein至pH 3。当溶解氧浓度较低(6.2877 mg/L)时,过氧化氢酶活性增加了23个酶单位。此外,本研究表明,Cr、Cu和Zn等重金属可以抑制鱼类各器官的生化反应。在混合金属离子作用期间,过氧化氢酶活性从35.89±1.02µmol H2O2/min/mg蛋白降低到23.51±2.85µmol H2O2/min/mg蛋白。另一方面,由于酶系统的响应,过氧化氢酶活性增加到36.25±3.22µmol H2O2/min/mg蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research on Some Freshwater Fish Catalase Activity - As a Potential Biomarker for Environmental Pollution
In the last decade studies show that water pollution is a very serious problem, especially since the degree of water pollution plays a key role in the growth and fish multiplication. As a biomarker of environmental pollution, antioxidant enzymes such as catalase (CAT; EC 1.11.1.6) play an essential role in preventing the harmful effects of heavy metals in the tissues of fish. These researches were carried out to investigate the effect of various environment conditions and some pollutant agents on oxidative stress in some aquatic organisms. The enzymatic assay of CAT (in fish organs, e.g., liver, kidney, gill, intestine and brain, as well as in mixture of these organs) was carried out according to standard enzyme assay protocol. The results showed decrease of CAT activity: the enzymatic activity was 35.89 ± 1.02 µmol H2O2/min/mg protein to pH 7 and 6.59 ± 0.47 µmol H2O2/min/mg protein to pH 12. More, the enzymatic activity was 38.1 ± 0.3 µmol H2O2/min/mg protein to pH 3. Also, the catalase activity increased with 23 enzymatic units to a less dissolved oxygen concentration (6.2877 mg/L). Furthermore, this study indicated that heavy metals, such as Cr, Cu and Zn can inhibit biochemical reactions in various organs of fish. During exposure duration of the fish to a mixture of metal ions the catalase activity decreases from 35.89 ± 1.02 µmol H2O2/min/mg protein to 23.51 ± 2.85 µmol H2O2/min/mg protein. On the other hand, as a result of the response of the enzyme system, the catalase activity increases to 36.25 ± 3.22 µmol H2O2/min/mg protein.
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