Novel insights into aerobic 17β-estradiol degradation by enriched microbial communities from mangrove sediments

雌酮 红树林 雌激素 环境化学 基因组 生物降解 生物 生物修复 细菌 化学 生物化学 生态学 基因 遗传学
作者
Shan Zhang,Xueying Ye,Xiaofan Lin,Xianying Zeng,Shanshan Meng,Wenqi Luo,Fei Yu,Tao Peng,Tongwang Huang,Jin Li,Zhong Hu
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:465: 133045-133045
标识
DOI:10.1016/j.jhazmat.2023.133045
摘要

Various persistent organic pollutants (POPs) including estrogens are often enriched in mangrove regions. This research investigated the estrogens pollution levels in six mangroves located in the Southern China. The estrogen levels were found to be in the range of 5.3 to 24.9 ng/g dry weight, suggesting that these mangroves had been seriously contaminated. The bacterial communities under estrogen stress were further enriched by supplementing 17β-estradiol (E2) as the sole carbon source. The enriched bacterial communities showed an excellent E2 degradation capacity > 95%. These communities were able to transform E2 into estrone (E1), 4-hydroxy-estrone, and keto-estrone, etc. 16 S rDNA sequencing and metagenomics analysis revealed that bacterial taxa Oleiagrimonas, Pseudomonas, Terrimonas, and Nitratireductor etc. were the main contributors to estrogen degradation. Moreover, the genes involved in E2 degradation were enriched in the microbial communities, including the genes encoding 17β-hydroxysteroid dehydrogenase, estrone 4-hydroxylase, etc. Finally, the analyses of functional genes and binning genomes demonstrated that E2 was degraded by bacterial communities via dehydrogenation into E1 by 17β-hydroxysteroid dehydrogenase. E1 was then catabolically converted to 3aα-H-4α(3′-propanoate)-7aβ-methylhexahydro-1,5-indanedione via 4,5-seco pathway. Alternatively, E1 could also be hydroxylated to keto-estrone, followed by B-ring cleavage. This study provides novel insights into the biodegradation of E2 by the bacterial communities in estrogen-contaminated mangroves. In this study, the highly efficient E2-degrading bacterial communities were obtained from E2-enriched culture. The highest E2 degradation rate of > 95% was achieved. The core E2-degrading bacterial communities were also identified. Moreover, 112 metagenome-assembled genomes (MAGs) were obtained. Interestingly, some of the MAGs harbored the functional genes involved in E2 transformation, but belonged to the genera which had not been reported in the previous studies. These results provide new insights into estrogen degradation by mangrove microbial communities. The findings of this study highlight the contribution and potential of bacterial communities to alleviate the estrogen contamination in mangrove forests. This work should be interesting to general readers of this journal.
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