School of Environment and Energy, South China University of Technology, Guangzhou, 510006, China.
School of Environment and Energy, South China University of Technology, Guangzhou, 510006, China; Key Laboratory of Ministry of Education on Pollution Control and Ecosystem Restoration in Industry Clusters, Guangzhou, 510006, China; Guangdong Provincial Key Laboratory of Solid Wastes Pollution Control and Recycling, Guangzhou, 510006, China.
Environ Pollut. 2022 Nov 15;313:120120. doi: 10.1016/j.envpol.2022.120120. Epub 2022 Sep 6.
The influence of biochar on the biodegradation of persistent organic pollutants (POPs) has been extensively studied. However, the underlying mechanisms behind the response of functional microbial consortia to biochar remain poorly understood. Herein, we systematically explored the effect of biochar on 2,2',4,4'-tetrabrominated ether (BDE-47) biodegradation, and investigated the interaction and assembly mechanism of the functional bacterial consortium QY2. The results revealed that the biodegradation efficiency of QY2 for BDE-47 increased from 53.85% to 94.11% after the addition of biochar. Fluorescence excitation-emission matrix and electrochemical analysis showed that biochar-attached biofilms were rich in redox-active extracellular polymeric substances (EPS, 3.03-fold higher than free cell), whose strong interaction with biochar facilitated the electron transfer of the biofilm, thus enhancing the debromination degradation of BDE-47. Meanwhile, the assembly model and molecular ecological networks analysis indicated that bacterial community assembly in biofilms was more driven by deterministic processes (environmental selection >75.00%) upon biochar stimulation and exhibited closer interspecific cooperative interactions, leading to higher biodiversity and broader habitat niche breadth for QY2 in response to BDE-47 disturbance. Potential degraders (Methylobacterium, Sphingomonas, Microbacterium) and electrochemical bacteria (Ochrobactrum) were selectively enriched, whose role as keystone bacteria may be participated in biofilm formation and redox-active EPS secretion (r > 0.5, P < 0.05). These findings deepen the understanding of the mechanisms by which biochar promotes microbial degradation of PBDEs and provided a theoretical basis for better regulation of functional bacterial communities during environmental remediation.
生物炭对持久性有机污染物(POPs)生物降解的影响已得到广泛研究。然而,功能微生物群落对生物炭响应的潜在机制仍知之甚少。在此,我们系统地研究了生物炭对 2,2',4,4'-四溴醚(BDE-47)生物降解的影响,并研究了功能细菌群落 QY2 的相互作用和组装机制。结果表明,生物炭的添加使 QY2 对 BDE-47 的生物降解效率从 53.85%提高到 94.11%。荧光激发-发射矩阵和电化学分析表明,生物炭附着生物膜富含氧化还原活性胞外聚合物物质(EPS,比游离细胞高 3.03 倍),其与生物炭的强烈相互作用促进了生物膜的电子转移,从而增强了 BDE-47 的脱溴降解。同时,组装模型和分子生态网络分析表明,生物炭刺激下生物膜中细菌群落的组装更多地受到确定性过程(环境选择>75.00%)的驱动,表现出更紧密的种间协同相互作用,导致 QY2 对 BDE-47 干扰的生物多样性和更广泛的栖息地宽度更高。潜在的降解菌(甲基杆菌、鞘氨醇单胞菌、微杆菌)和电化学细菌(真杆菌)被选择性富集,它们作为关键菌的作用可能参与了生物膜的形成和氧化还原活性 EPS 的分泌(r>0.5,P<0.05)。这些发现加深了对生物炭促进多溴二苯醚微生物降解机制的理解,并为环境修复过程中更好地调节功能细菌群落提供了理论依据。