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三电极微生物电化学系统中磺胺甲恶唑的降解:有机污染影响的代谢组学和宏基因组学见解。

Sulfamethoxazole degradation in tri-electrode microbial electrochemical systems: Metabolomic and Metagenomic insights into organic pollution effects.

机构信息

School of Energy and Environment, Southeast University, Nanjing, 210096, China.

State Key Laboratory of Eco-Hydraulics in Northwest Arid Region, Department of Municipal and Environmental Engineering, Faculty of Water Resources and Hydroelectric Engineering, Xi'an University of Technology, Xi'an, 710048, China.

出版信息

J Environ Manage. 2024 Nov;370:122410. doi: 10.1016/j.jenvman.2024.122410. Epub 2024 Sep 8.

Abstract

Organic pollutants can alter the physicochemical properties and microbial communities of water bodies. In water contaminated with organic pollutants, the unique extracellular electron transfer mechanisms that promote sulfamethoxazole (SMX) degradation in tri-electrode microbial electrochemical systems (TE-MES) may be impacted. To simulate biodegradable organic matter contamination, glucose (GLU) was added. Metagenomics and metabolomics were used to analyze changes in microbial community structure, metabolism, and function on the electrodes. GLU addition accelerated water quality deterioration, and enhanced SMX degradation. Microbial taxa on the electrodes experienced selective enrichment. Notably, methanogens and SMX-degrading bacteria were enriched, while denitrifying bacteria and antibiotic-resistant bacteria were suppressed. Enriched metabolites were linked to 15 metabolic pathways and other functions like microbial signaling and genetics. Non-redundant genes also clustered in metabolic pathways, aligning with metabolite enrichment results. Additional pathways involved life cycle processes and protein interactions. Enzymes related to carbon metabolism, particularly glycoside hydrolases, increased significantly, indicating a shift in carbon metabolism on microbial electrodes after GLU addition. The abundance of intracellular electron transfer enzymes rose, while outer membrane proteins decreased. This contrasts with the typical TE-MES mechanism where outer membrane proteins facilitate SMX degradation. The presence of organic pollution may shift SMX degradation from an extracellular electrochemical process to an intracellular metabolic process, possibly involving co-metabolism with simple organic compounds. This study provides mechanistic insights and theoretical guidance for using TE-MES with embedded microbial electrodes to treat antibiotic-contaminated water affected by organic pollution.

摘要

有机污染物会改变水体的物理化学性质和微生物群落。在受有机污染物污染的水中,促进三电极微生物电化学系统(TE-MES)中磺胺甲恶唑(SMX)降解的独特胞外电子传递机制可能会受到影响。为了模拟可生物降解有机物的污染,添加了葡萄糖(GLU)。利用宏基因组学和代谢组学分析了电极上微生物群落结构、代谢和功能的变化。GLU 的添加加速了水质恶化,并增强了 SMX 的降解。电极上的微生物类群经历了选择性富集。值得注意的是,产甲烷菌和 SMX 降解菌得到了富集,而反硝化菌和抗生素抗性菌受到了抑制。富集的代谢物与 15 条代谢途径以及微生物信号转导和遗传等其他功能有关。非冗余基因也聚类在代谢途径中,与代谢物富集结果一致。其他途径涉及生命周期过程和蛋白质相互作用。与碳代谢有关的酶,特别是糖苷水解酶,显著增加,表明 GLU 添加后微生物电极上的碳代谢发生了转变。细胞内电子转移酶的丰度增加,而外膜蛋白减少。这与典型的 TE-MES 机制形成对比,后者外膜蛋白促进 SMX 的降解。有机污染物的存在可能会将 SMX 的降解从胞外电化学过程转变为胞内代谢过程,可能涉及与简单有机化合物的共代谢。本研究为使用嵌入微生物电极的 TE-MES 处理受有机污染影响的抗生素污染水提供了机制见解和理论指导。

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