College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China.
College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China; School of Life Science, Jinggangshan University, Ji'an 343009, China.
J Hazard Mater. 2016 Mar 15;305:123-129. doi: 10.1016/j.jhazmat.2015.11.037. Epub 2015 Nov 23.
Antibiotics are categorized as pseudopersistent compounds because of their widespread use and continuous emission into the environment. Biological systems such as active sludge and biofilms are still the principal tools used to remove antibiotics in wastewater treatment plants (WWTPs). Consequently, it is important to determine the relationship between toxic effects in biological WWTPs and the structural characteristics of antibiotics. In the present study, toxic effects of 10 sulfonamides (SAs) on nitrification in an active sludge system were studied. The toxicity results (half-effective concentrations, EC50) indicated that the toxicity of sulfadimethoxine (SDM) is approximately 4 times as large as that of sulfadiazine (SD). Based on the toxicity mechanism and the partial least squares regression (PLS) method, an optimum quantitative structure-activity relationship (QSAR) model was developed for the test system. The mechanistic model showed that the pKa, the binding energies between SAs with dihydropteroate synthetase ( [Formula: see text] ) and the binding energies between SAs with ammonia monooxygenase ( [Formula: see text] ) are the key factors affecting the toxic effects of SAs on nitration process in active sludge system, following an order of importance of [Formula: see text] > [Formula: see text] >pKa.
抗生素因其广泛使用和持续向环境排放而被归类为假持久性化合物。活性污泥和生物膜等生物系统仍然是废水处理厂(WWTP)中去除抗生素的主要工具。因此,确定生物 WWTP 中的毒性效应与抗生素的结构特征之间的关系非常重要。在本研究中,研究了 10 种磺胺类药物(SAs)对活性污泥系统硝化作用的毒性效应。毒性结果(半有效浓度,EC50)表明,磺胺二甲氧嘧啶(SDM)的毒性约为磺胺嘧啶(SD)的 4 倍。基于毒性机制和偏最小二乘回归(PLS)方法,为测试系统开发了最佳的定量构效关系(QSAR)模型。该机理模型表明,pKa、磺胺类药物与二氢叶酸合成酶([公式:见文本])的结合能以及磺胺类药物与氨单加氧酶([公式:见文本])的结合能是影响磺胺类药物对活性污泥系统硝化过程毒性效应的关键因素,重要性顺序为[公式:见文本]>[公式:见文本]>pKa。