Al-Maqdi Khadega A, Hisaindee Soleiman M, Rauf Muhammad A, Ashraf Syed Salman
Department of Chemistry, UAE University, P.O. Box 15551, Al-Ain, UAE.
Biomolecules. 2017 Aug 24;7(3):64. doi: 10.3390/biom7030064.
Organic pollutants, especially those found in water bodies, pose a direct threat to various aquatic organisms as well as humans. A variety of different remediation approaches, including chemical and biological methods, have been developed for the degradation of various organic pollutants. However, comparative mechanistic studies of pollutant degradation by these different systems are almost non-existent. In this study, the degradation of a model thiazole pollutant, thioflavin T (ThT), was carried out in the presence of either an advanced oxidation process (ultraviolet (UV) + H₂O₂) or a chloroperoxidase enzyme system (CPO + H₂O₂). The degradation was followed both spectrophotometrically and using liquid chromatography-mass spectroscopy (LC-MS), and the products formed were identified using tandem liquid chromatography-mass spectrometry-mass spectrometry (LC-MS-MS). The results show that the two remediation approaches produced different sets of intermediates, with only one common species (a demethylated form of ThT). This suggests that different degradation schemes were operating in the two systems. Interestingly, one of the major intermediates produced by the CPO + H₂O₂ system was a chlorinated form of thioflavin. Phytotoxicity studies showed that the CPO + H₂O₂-treated ThT solution was significantly ( <0.05) less toxic than the UV + H₂O₂-treated ThT solution. This is the first time that a comparative mechanistic study showing in detail the intermediates generated in chemical and biological remediation methods has been presented. Furthermore, the results show that different remediation systems have very different degradation schemes and result in products having different toxicities.
有机污染物,尤其是水体中发现的那些,对各种水生生物以及人类构成直接威胁。为了降解各种有机污染物,已经开发了多种不同的修复方法,包括化学和生物方法。然而,关于这些不同系统对污染物降解的比较机理研究几乎不存在。在本研究中,在高级氧化过程(紫外线(UV)+H₂O₂)或氯过氧化物酶系统(CPO+H₂O₂)存在的情况下,对模型噻唑污染物硫代黄素T(ThT)进行了降解。通过分光光度法和液相色谱-质谱联用(LC-MS)跟踪降解过程,并使用串联液相色谱-质谱-质谱联用(LC-MS-MS)鉴定形成的产物。结果表明,两种修复方法产生了不同的中间产物组,只有一种共同的物种(ThT的去甲基化形式)。这表明两个系统中运行着不同的降解方案。有趣的是,CPO+H₂O₂系统产生的主要中间产物之一是硫代黄素的氯化形式。植物毒性研究表明,CPO+H₂O₂处理的ThT溶液的毒性明显(<0.05)低于UV+H₂O₂处理的ThT溶液。这是首次详细展示化学和生物修复方法中产生的中间产物的比较机理研究。此外,结果表明不同的修复系统具有非常不同的降解方案,并导致产物具有不同的毒性。