中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Fast coupling and detoxification of aqueous halobenzoquinones by extracellular nucleophiles: The relationship among structures, pathways and toxicity

文献类型:期刊论文

作者Zhong, Chen1,2,4; Zhao, He1,2,4; Cao, Hongbin1,2,4; Huang, Ching-Hua3
刊名CHEMICAL ENGINEERING JOURNAL
出版日期2022-06-15
卷号438页码:13
ISSN号1385-8947
关键词Dichlorobenzoquinone Nucleophiles Transformation pathways Toxicity Density functional theory
DOI10.1016/j.cej.2022.135525
英文摘要Halobenzoquinones (HBQs), a metabolism of pentachlorophenol, arouse increasing concern for their high toxicity. This paper systematically studied the influences of 31 extracellular nucleophiles on the removal of dichlorobenzoquinones (DCBQs). The results showed that at pH 6.0-8.0, the transformation of DCBQs followed a pattern of pseudo first-order reaction. With the presence of different thiol compound (ratio 1:1), the apparent rate constant of 25DCBQ and 26DCBQ was between 0.028 and 0.204 min-1 and 0.061-0.156 min-1, respectively, which was 6.6-48.3 times faster than direct hydrolysis and 1.9-23.4 times of that with histidine, a typical amino acid. This was attributed to the different transformation pathways of DCBQs with thiol or amino groups. According to the MS spectrum and transition state theory, thiol compounds was stably incorporated into DCBQs via Michael addition or substitution, which also decreased the oxidative stress of DCBQs by 35.5-86.4% and cytotoxicity of hydrolyzed DCBQ by 44.9-100%, respectively. Conversely, amino acids promoted the hydrolysis of DCBQs by forming unstable AA-DCBQ intermediates that can be further hydrolyzed to OH-DCBQs, leading to an increased selectivity of OH-DCBQs, and increased the oxidative stress of 25DCBQs by 0.2-31.2% and cytotoxicity of hydrolyzed 25DCBQ by 42.0-52.7%. Such difference was inherently related to the nucleophilicity of different atoms. Moreover, it was revealed that the maximum condensed local nucleophilicity index of nucleophiles (Nk, max) can joint describe the relationship among nucleophilic structures, transformation pathways and toxicity of DCBQs. This paper provided a comprehensive perspective on the fast removal and detoxification of HBQs in extracellular environment.
WOS关键词METAL-INDEPENDENT DECOMPOSITION ; ORGANIC HYDROPEROXIDES ; LIQUID-CHROMATOGRAPHY ; MOLECULAR-MECHANISM ; HYDROXYL RADICALS ; HYDROGEN-PEROXIDE ; AMINO-ACIDS ; WATER ; PHARMACOKINETICS ; PHARMACEUTICALS
资助项目National Natural Science Foundation of China[51978643] ; Youth Innovation Promotion Association, CAS[2014037]
WOS研究方向Engineering
语种英语
出版者ELSEVIER SCIENCE SA
WOS记录号WOS:000779661100004
资助机构National Natural Science Foundation of China ; Youth Innovation Promotion Association, CAS
源URL[http://ir.ipe.ac.cn/handle/122111/52859]  
专题中国科学院过程工程研究所
通讯作者Zhao, He
作者单位1.Chinese Acad Sci, Inst Proc Engn, Natl Key Lab Biochem Engn, Beijing, Peoples R China
2.Beijing Engn Res Ctr Proc Pollut Control, Beijing, Peoples R China
3.Georgia Inst Technol, Sch Civil & Environm Engn, Atlanta, GA 30332 USA
4.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Zhong, Chen,Zhao, He,Cao, Hongbin,et al. Fast coupling and detoxification of aqueous halobenzoquinones by extracellular nucleophiles: The relationship among structures, pathways and toxicity[J]. CHEMICAL ENGINEERING JOURNAL,2022,438:13.
APA Zhong, Chen,Zhao, He,Cao, Hongbin,&Huang, Ching-Hua.(2022).Fast coupling and detoxification of aqueous halobenzoquinones by extracellular nucleophiles: The relationship among structures, pathways and toxicity.CHEMICAL ENGINEERING JOURNAL,438,13.
MLA Zhong, Chen,et al."Fast coupling and detoxification of aqueous halobenzoquinones by extracellular nucleophiles: The relationship among structures, pathways and toxicity".CHEMICAL ENGINEERING JOURNAL 438(2022):13.

入库方式: OAI收割

来源:过程工程研究所

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