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Anode potentials regulate Geobacter biofilms: New insights from the composition and spatial structure of extracellular polymeric substances

生物膜 地杆菌 胞外聚合物 阳极 细胞外 硫化地杆菌 生物物理学 化学 胞外多糖 多糖 电子转移 电化学 化学工程 微生物燃料电池 电极 氧化还原 舍瓦内拉 微生物学 环境化学 吸附 电解质 纳米技术 细菌 材料科学 生物化学 无机化学 生物 光化学 有机化学 遗传学 物理化学 工程类
作者
Guiqin Yang,Lingyan Huang,Zhen Yu,Xiaoming Liu,Shanshan Chen,Jianxiong Zeng,Shungui Zhou,Zhuang Li
出处
期刊:Water Research [Elsevier]
卷期号:159: 294-301 被引量:114
标识
DOI:10.1016/j.watres.2019.05.027
摘要

The extracellular electron transfer (EET) efficiency in bioelectrochemical systems has been proven to be dependent on anode potentials. To explore the underlying mechanism, previous studies have mainly focused on EET conduit and bacterial biomass but rarely concerned with the role of extracellular polymeric substances (EPS) surrounding electroactive cells. In this study, the response of Geobacter biofilms to anode potentials was investigated with a special emphasis on the mechanistic role of EPS. The electrochemical activities and cell viabilities of Geobacter soli biofilms were simultaneously attenuated at 0.4 and 0.6 V compared to −0.2 and 0 V. It was found that the biofilms (especially the biofilm region closer to electrode surface) grown at −0.2 and 0 V produced relatively more extracellular redox-active proteins and less extracellular polysaccharides, which conferred higher electron accepting/donating capacities to EPS and consequently facilitated EET. Meanwhile, electrically nonconductive extracellular polysaccharide-dominated interior layers were formed in the biofilms grown at 0.4 and 0.6 V, which limited direct EET but might serve as physical barriers for protecting cells in these biofilms from the increasing stress by poised electrodes. These results demonstrated that the production of EPS under different anode potentials might be finely regulated by cells to keep balance between EET efficiency and cell-protection. This study provides a new insight to investigate the Geobacter biofilms coping with various environments, and is useful for optimizing electrochemical activity of anode biofilms.
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