Elimination of endocrine disrupting chemicals nonylphenol and bisphenol A and personal care product ingredient triclosan using enzyme preparation from the white rot fungus Coriolopsis polyzona

被引:164
作者
Cabana, Hubert
Jiwan, Jean-Louis Habib
Rozenberg, Raoul
Elisashvili, Vladimir
Penninckx, Michel
Agathos, Spiros N.
Jones, J. Peter
机构
[1] Univ Sherbrooke, Dept Chem Engn, Sherbrooke, PQ J1K 2R1, Canada
[2] Catholic Univ Louvain, Bioengn Unit, B-1348 Louvain, Belgium
[3] Catholic Univ Louvain, Mass Spect Lab, B-1348 Louvain, Belgium
[4] Georgian Acad Sci, Drumishidze Inst Biochem & Biotechnol, GE-0159 Tbilisi, Georgia
[5] Univ Libre Bruxelles, Inst Pasteur, Fac Sci, Lab Microbial Physiol & Ecol, B-1180 Brussels, Belgium
基金
加拿大自然科学与工程研究理事会;
关键词
laccase; estrogenic activity; polymerization; mediators;
D O I
10.1016/j.chemosphere.2006.10.037
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The biocatalytic elimination of the endocrine disrupting chemicals (EDC) nonylphenol (NP) and bisphenol A (BPA) and the personal care product ingredient triclosan (TCS) by the enzyme preparation from the white rot fungus Coriolopsis polyzona was investigated. Analysis of variance methodology showed that the pH and the temperature are statistically significant factors in the removal of NP, BPA and TCS. The elimination of NP and TCS was best at a temperature of 50 degrees C and the disappearance of BPA at 40 degrees C, whereas the most suitable pH for all three micropollutants was 5. After a 4-h treatment of the three target compounds at concentrations of 5 mg l(-1) all of the NP and BPA were eliminated. In the case of TCS, 65% was removed after either a 4 or an 8-h treatment. The utilisation of 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) in the laccase/mediator system significantly increased the efficiency of the enzymatic treatment. The elimination of NP and BPA was directly associated with the disappearance of the estrogenic activity. Mass spectrometry analysis showed that the enzymatic treatment produced high molecular weight metabolites through a radical polymerization mechanism of NP, BPA and TCS. These oligomers were produced through the formation of C-C or C-O bonds. The polymerization of NP produced dimers, trimers, tetramers and pentamers which had molecular weights of 438, 656, 874 and 1092 amu respectively. The polymerization of BPA produced dimers, trimers and tetramers which had molecular weights of 454, 680 and 906 amu. Finally, the polymerization of TCS produced dimers, trimers and tetramers which had molecular weights of 574, 859 and 1146 amu. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:770 / 778
页数:9
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