张旭旺

(副教授)

 硕士生导师
学位:博士
性别:男
毕业院校:大连理工大学
所在单位:化工海洋与生命学院
电子邮箱:zhangxw@dlut.edu.cn

论文成果

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Comparative characterization and functional genomic analysis of two Comamonas sp. strains for biodegradation of quinoline

发表时间:2020-08-23 点击次数:

论文名称:Comparative characterization and functional genomic analysis of two Comamonas sp. strains for biodegradation of quinoline
论文类型:期刊论文
第一作者:Zhang, Xuwang
通讯作者:Zhang, XW (reprint author), Dalian Univ Technol, Minist Educ, Sch Ocean Sci & Technol, Key Lab Ind Ecol & Environm Engn, Panjin 124221, Peoples R China.
合写作者:Zhang, Lizhi,Wu, Minghuo,Tang, Qidong,Song, Zhaojian,Zhou, Hao,Bao, Yongming,Liu, Lifen,Qu, Yuanyuan
发表刊物:JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
收录刊物:SCIE
卷号:95
期号:7
页面范围:2017-2026
ISSN号:0268-2575
关键字:quinoline; Comamonas; biodegradation; pathway; genome
摘要:BACKGROUND Quinoline is an ubiquitous pollutant widely spread in the environment, which can be eliminated efficiently by microbial degradation. In this study, two quinoline-degrading Comamonas sp. strains Z1 and Z3 were isolated from activated sludge, and the degradation characteristics and genome annotation were investigated in detail.
   RESULTS Strain Z1 exhibited a superior capacity for quinoline degradation, which could completely degrade 50-300 mg L-1 quinoline within 8-24 h, whereas strain Z3 required 14-36 h to remove 50-200 mg L-1 quinoline. The suitable pHs for strains Z1 and Z3 were 8.0 and 7.0, respectively, and metal ions such as Mn2+, Ni2+, Cu2+, Co2+ and Hg2+ could greatly inhibit bacterial growth and quinoline degradation. Intermediates of 2-hydroxyquinoline, 2,8-dihydroxyquinoline, 8-hydroxycoumarin, 2,3-dihydroxyphenylpropionic acids and 2-hydroxy-6-oxonona-2,4-diene-1,9-dioate were detected by liquid chromatography coupled to Q-Exactive high-resolution mass spectrometry. Thus, the biodegradation of quinoline by Comamonas sp. strains possibly proceeded via the 8-hydroxycoumarin pathway. Genomic sequencing of strains Z1 and Z3 revealed a similar pattern, and a large number of functional genes were predicted to participate in degradation of aromatics. The key genes responsible for quinoline degradation also were identified, such as qor, mhp and bph. Furthermore, quinoline 2-oxidoreductase (Qor) from strains Z1 and Z3 displayed 47.74%-61.17% similarities with previously reported Qor, which catalyzed the first step of quinoline degradation, and the maximal specific activity in cell-free extracts of strains Z1 and Z3 was 0.264 and 0.062 U mg protein(-1), respectively.
   CONCLUSION This study should provide efficient microbial resources and useful genomic information for quinoline bioremediation. (c) 2020 Society of Chemical Industry
发表时间:2020-07-01