Qing Jiang , Xing Dong , Yang Liu , Xiaoyu Zhou , Guomeng Sun , Ke Shi , Yanlu Qiao , Hao Jiang , Yujie Feng
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引用次数: 0
Abstract
This study first evaluated the sulfamethoxazole (SMX) effects on oxygen-reducing biocathodes in microbial fuel cells (MFCs). Low SMX (0.5 mg L–1) enhanced current density by 20 % via increased direct electron transfer and lower charge transfer resistance. High SMX (10–30 mg L–1) suppressed electrochemical performance. SMX preferentially bound protein-like EPS components over fulvic-like fractions, inducing sequential structural changes (1054 > 970 > 3464 > 2921 > 1643 > 1350 cm−1). SMX exposure reshaped microbial communities, enriching antibiotic-resistant genera (Truepera, Nitrospira, Brevundimonas, etc.). Network analysis revealed low SMX enhanced community complexity/stability, while high doses simplified biofilm structure. Functional genes for electron transfer, carbon metabolism and oxidative phosphorylation increased at 0.5 mg L–1 SMX but decreased under high concentrations. Overall, this study elucidates the dual role of SMX in modulating oxygen-reducing biofilm composition, function, and capability, laying the groundwork for optimized application of MFC in treating SMX-contaminated wastewater.
期刊介绍:
Bioresource Technology publishes original articles, review articles, case studies, and short communications covering the fundamentals, applications, and management of bioresource technology. The journal seeks to advance and disseminate knowledge across various areas related to biomass, biological waste treatment, bioenergy, biotransformations, bioresource systems analysis, and associated conversion or production technologies.
Topics include:
• Biofuels: liquid and gaseous biofuels production, modeling and economics
• Bioprocesses and bioproducts: biocatalysis and fermentations
• Biomass and feedstocks utilization: bioconversion of agro-industrial residues
• Environmental protection: biological waste treatment
• Thermochemical conversion of biomass: combustion, pyrolysis, gasification, catalysis.