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长期盐酸四环素胁迫下nZVI-C对厌氧氨氧化菌群落抑制的缓解机制:胞外聚合物特性及微生物群落演变

Mitigating mechanism of nZVI-C on the inhibition of anammox consortia under long-term tetracycline hydrochloride stress: Extracellular polymeric substance properties and microbial community evolution.

作者信息

Zhang Li, Song Zixuan, Dong Tingjun, Fan Xuepeng, Peng Yongzhen, Yang Jiachun

机构信息

National Engineering Laboratory for Advanced Municipal Wastewater Treatment and Reuse Technology, Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124, China.

National Engineering Laboratory for Advanced Municipal Wastewater Treatment and Reuse Technology, Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124, China.

出版信息

J Hazard Mater. 2023 Jun 15;452:131035. doi: 10.1016/j.jhazmat.2023.131035. Epub 2023 Feb 21.

Abstract

In this study, activated carbon-loaded nano-zero-valent iron (nZVI-C) composites were added to anaerobic ammonium oxidation bacteria (AnAOB) to overcome the inhibition of tetracycline hydrochloride (TCH). Results showed that 500 mg L nZVI-C effectively mitigated the long-term inhibition of 1.5 mg L TCH on AnAOB and significantly improved the total nitrogen removal efficiency (TNRE) (from 65.27% to 86.99%). Spectroscopic analysis revealed that nZVI-C increased the content of N-H and CO groups in EPS, which contributed to the adsorption of TCH. The accumulation of humic acid-like substances in EPS was also conducive to strengthening the extracellular defense level. In addition, TCH-degrading bacteria (Clostridium and Mycobacterium) were enriched in situ, and the abundance of Ca. Brocadia was significantly increased (from 10.69% to 18.59%). Furthermore, nZVI-C increased the abundance of genes encoding tetracycline inactivation (tetX), promoted mineralization of TCH by 90%, weakening the inhibition of TCH on microbial nitrogen metabolism. nZVI-C accelerated the electron consumption of anammox bacteria by upregulating the abundance of electron generation genes (nxrA, hdh) and providing electrons directly.

摘要

在本研究中,将负载活性炭的纳米零价铁(nZVI-C)复合材料添加到厌氧氨氧化细菌(AnAOB)中,以克服盐酸四环素(TCH)的抑制作用。结果表明,500 mg/L的nZVI-C有效减轻了1.5 mg/L TCH对AnAOB的长期抑制作用,并显著提高了总氮去除效率(TNRE)(从65.27%提高到86.99%)。光谱分析表明,nZVI-C增加了EPS中N-H和CO基团的含量,这有助于TCH的吸附。EPS中类腐殖酸物质的积累也有利于提高细胞外防御水平。此外,TCH降解细菌(梭菌属和分枝杆菌属)原位富集,Ca. Brocadia的丰度显著增加(从10.69%增加到18.59%)。此外,nZVI-C增加了编码四环素失活的基因(tetX)的丰度,使TCH的矿化作用提高了90%,减弱了TCH对微生物氮代谢的抑制作用。nZVI-C通过上调电子生成基因(nxrA、hdh)的丰度并直接提供电子,加速了厌氧氨氧化细菌的电子消耗。

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