He Ronghui, Sun Jian, Yuan Yong, Bai Xiaoyan, Lin Qintie, Zhang Yaping, Dai Kang, Xu Zhenbo
Guangzhou Key Laboratory Environmental Catalysis and Pollution Control, Guangdong Key Laboratory of Environmental Catalysis and Health Risk Control, School of Environmental Science and Engineering, Institute of Environmental Health and Pollution Control, Guangdong University of Technology, Guangzhou 510006, China; South China Institute of Environmental Sciences, Ministry of Ecology and Environment, Guangzhou 510655, China; Guangdong Engineering & Technology Research Center for System Control of Livestock and Poultry Breeding Pollution, Guangzhou 510655, China.
Guangzhou Key Laboratory Environmental Catalysis and Pollution Control, Guangdong Key Laboratory of Environmental Catalysis and Health Risk Control, School of Environmental Science and Engineering, Institute of Environmental Health and Pollution Control, Guangdong University of Technology, Guangzhou 510006, China.
J Hazard Mater. 2025 May 5;488:137403. doi: 10.1016/j.jhazmat.2025.137403. Epub 2025 Jan 27.
Extracellular polymeric substances (EPS) are promising biomaterials for environmental remediation, but their application is hindered by low production efficiency and limited pollutant degradation capacity. In this study, photosynthetic electron extraction enabled Rhodopseudomonas palustris (R. palustris) to efficiently produce EPS enriched with functionalized components. The enhanced EPS (0.2V-EPS), produced from electrically domesticated R. palustris, achieved an 82 % degradation rate of sulfamethoxazole (SMX) within 10 hours, an 18 % improvement compared to EPS produced under open-circuit conditions (OP-EPS). Mechanistic analysis revealed that photosynthetic electron extraction enriched EPS with photosensitive molecules, including tryptophan, humic acid, fulvic acid, which significantly promoted the generation of reactive species. The primary reactive species identified were triplet-excited EPS (³EPS*), ¹O₂, and •OH, with ¹O₂ as the dominant contributor to SMX degradation. The steady-state concentration of ³EPS*, ¹O₂, and •OH increased by 73 %, 34 % and 16 %, respectively, compared to the control. Structural modifications of 0.2V-EPS, including increased hydrophilicity, electronegativity, and aromaticity, enhance its physicochemical properties, thereby facilitating interactions with pollutants. Furthermore, an 88 % reduction in biofilm polysaccharides diminished free radical scavenging activity, promoting the generation of reactive species. This study provides a sustainable strategy for enhancing EPS functionality and offers insights into the metabolic regulation of microorganisms for pollutant degradation.
胞外聚合物(EPS)是用于环境修复的有前景的生物材料,但其应用受到生产效率低和污染物降解能力有限的阻碍。在本研究中,光合电子提取使沼泽红假单胞菌(R. palustris)能够高效生产富含功能化成分的EPS。由电驯化的R. palustris产生的增强型EPS(0.2V-EPS)在10小时内实现了82%的磺胺甲恶唑(SMX)降解率,与开路条件下产生的EPS(OP-EPS)相比提高了18%。机理分析表明,光合电子提取使EPS富含光敏分子,包括色氨酸、腐殖酸、富里酸,这显著促进了活性物种的产生。确定的主要活性物种为三线态激发的EPS(³EPS*)、¹O₂和•OH,其中¹O₂是SMX降解的主要贡献者。与对照相比,³EPS*、¹O₂和•OH的稳态浓度分别增加了73%、34%和16%。0.2V-EPS的结构修饰,包括亲水性、电负性和芳香性的增加,增强了其物理化学性质,从而促进了与污染物的相互作用。此外,生物膜多糖减少88%降低了自由基清除活性,促进了活性物种的产生。本研究为增强EPS功能提供了一种可持续策略,并为微生物代谢调控污染物降解提供了见解。