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Fe(III)-Aided Novosphingobium sp. ES2-1 Regulates Molecular Mechanisms of 17β-Estradiol Biodegradation

文献类型： 外文期刊

作者： Li, Shunyao 1 ; Wang, Yiru 1 ; Sun, Kai 3 ; Li, Yuxin 1 ; Lu, Chao 2 ; Gao, Yanzheng 5 ;

作者机构： 1.Anhui Univ, Sch Resources & Environm Engn, Anhui Prov Key Lab Wetland Ecosyst Protect & Resto, Hefei 230601, Anhui, Peoples R China

2.Jiangsu Acad Agr Sci, Inst Agr Resources & Environm, Natl Agr Expt Stn Agr Environm, Nanjing 210014, Jiangsu, Peoples R China

3.Anhui Agr Univ, Coll Resources & Environm, Hefei 230036, Anhui, Peoples R China

4.Univ Sci & Technol China, Dept Environm Sci & Engn, CAS Key Lab Urban Pollutant Convers, Hefei 230026, Anhui, Peoples R China

5.Nanjing Agr Univ, Inst Organ Contaminant Control & Soil Remediat, Coll Resources & Environm Sci, Nanjing 210095, Jiangsu, Peoples R China

关键词： environmental estrogens; Novosphingobium; biodegradationkinetics; dioxygenase EstN1; Fe(III)-aided bioremediation; molecular mechanisms

期刊名称：ENVIRONMENTAL SCIENCE & TECHNOLOGY （ 影响因子：11.3； 五年影响因子：12.4 ）

ISSN： 0013-936X

年卷期： 2024 年 58 卷 50 期

页码：

收录情况： SCI

摘要： 17 beta-estradiol (E2) is one of the strongest environmental estrogens threatening wildlife and human health globally. Microbial degradation is an alternative strategy to remediate E2-contaminated sites and may be regulated by ubiquitous Fe(III) in eco-environments. We have previously obtained a high-efficiency E2 degrader, Novosphingobium sp. ES2-1, and investigated its metabolic pathway in connection with monooxygenase EstO1-induced ring-B opening; however, the molecular mechanisms of ring-A cleavage in E2 are sorely lacking, especially under Fe(III)-aided regulation. Here, an extradiol dioxygenase EstN1 from strain ES2-1 involved in the ring-A cleavage of E2 was reported. It catalyzed the 4,5-seco reaction of 4-hydroxyestrone (4-OH-E1, a key E2-oxidized intermediate) with the support of the electron transport chain consisting of ferredoxin EstN2 and ferredoxin reductase EstN3, resulting in a ring-A meta-cleaved product. Interestingly, Fe(III)-assisted strain ES2-1 consolidated the opening of rings A and B in E2 by reinforcing the expression of estO1 and estN1 genes, consequently enhancing E2 metabolism. Compared to Fe(III) starvation, the biodegradation half-life of E2 was sharply reduced from 1.35 to 0.59 d after Fe(III) supplementation. Simultaneously, the transcription of estO1 and estN1 genes increased clearly from 4.3 to 47.5 times and 6.6 to 246.8 times after Fe(III) induction, respectively, accompanied by remarkable improvement in the abundance of ring-A/B cleavage products and their pyridine derivatives. These findings highlight the significance of Fe(III) in regulating the microbial remediation of environmental estrogens at the molecular level.

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