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Electricity Production byGeobacter sulfurreducensAttached to Electrodes

硫化地杆菌 电子受体 微生物燃料电池 电极 无氧呼吸 地杆菌 电子转移 化学 标准氢电极 无机化学 电化学 无氧运动 参比电极 生物化学 细菌 光化学 生物 阳极 物理化学 生物膜 遗传学 生理学
作者
Daniel R. Bond,Derek R. Lovley
出处
期刊:Applied and Environmental Microbiology [American Society for Microbiology]
卷期号:69 (3): 1548-1555 被引量:2157
标识
DOI:10.1128/aem.69.3.1548-1555.2003
摘要

ABSTRACT Previous studies have suggested that members of the Geobacteraceae can use electrodes as electron acceptors for anaerobic respiration. In order to better understand this electron transfer process for energy production, Geobacter sulfurreducens was inoculated into chambers in which a graphite electrode served as the sole electron acceptor and acetate or hydrogen was the electron donor. The electron-accepting electrodes were maintained at oxidizing potentials by connecting them to similar electrodes in oxygenated medium (fuel cells) or to potentiostats that poised electrodes at +0.2 V versus an Ag/AgCl reference electrode (poised potential). When a small inoculum of G. sulfurreducens was introduced into electrode-containing chambers, electrical current production was dependent upon oxidation of acetate to carbon dioxide and increased exponentially, indicating for the first time that electrode reduction supported the growth of this organism. When the medium was replaced with an anaerobic buffer lacking nutrients required for growth, acetate-dependent electrical current production was unaffected and cells attached to these electrodes continued to generate electrical current for weeks. This represents the first report of microbial electricity production solely by cells attached to an electrode. Electrode-attached cells completely oxidized acetate to levels below detection (<10 μM), and hydrogen was metabolized to a threshold of 3 Pa. The rates of electron transfer to electrodes (0.21 to 1.2 μmol of electrons/mg of protein/min) were similar to those observed for respiration with Fe(III) citrate as the electron acceptor (E o ′ =+0.37 V). The production of current in microbial fuel cell (65 mA/m 2 of electrode surface) or poised-potential (163 to 1,143 mA/m 2 ) mode was greater than what has been reported for other microbial systems, even those that employed higher cell densities and electron-shuttling compounds. Since acetate was completely oxidized, the efficiency of conversion of organic electron donor to electricity was significantly higher than in previously described microbial fuel cells. These results suggest that the effectiveness of microbial fuel cells can be increased with organisms such as G. sulfurreducens that can attach to electrodes and remain viable for long periods of time while completely oxidizing organic substrates with quantitative transfer of electrons to an electrode.

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