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通过在微生物燃料电池中操纵辅助因子来增强生物电能的产生。

Enhancement of bioelectricity generation by cofactor manipulation in microbial fuel cell.

机构信息

College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 210009, China; Bioenergy Research Institute, Nanjing University of Technology, Nanjing 210009, China.

College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 210009, China.

出版信息

Biosens Bioelectron. 2014 Jun 15;56:19-25. doi: 10.1016/j.bios.2013.12.058. Epub 2014 Jan 2.

DOI:10.1016/j.bios.2013.12.058
PMID:24445069
Abstract

Microbial fuel cells (MFCs) are promising for harnessing bioenergy from various organic wastes. However, low electricity power output (EPT) is one of the major bottlenecks in the practical application of MFCs. In this study, EPT improvement by cofactor manipulation was explored in the Pseudomonas aeruginosa-inoculated MFCs. By overexpression of nadE (NAD synthetase gene), the availability of the intracellular cofactor pool (NAD(H/(+))) significantly increased, and delivered approximately three times higher power output than the original strain (increased from 10.86 μW/cm(2) to 40.13 μW/cm(2)). The nadE overexpression strain showed about a onefold decrease in charge transfer resistance and higher electrochemical activity than the original strain, which should underlie the power output improvement. Furthermore, cyclic voltammetry, HPLC, and LC-MS analysis showed that the concentration of the electron shuttle (pyocyanin) increased approximately 1.5 fold upon nadE overexpression, which was responsible for the enhanced electrochemical activity. Thus, the results substantiated that the manipulation of intracellular cofactor could be an efficient approach to improve the EPT of MFCs, and implied metabolic engineering is of great potential for EPT improvement.

摘要

微生物燃料电池(MFCs)有望从各种有机废物中获取生物能源。然而,低电能输出(EPT)是 MFC 实际应用中的主要瓶颈之一。在本研究中,通过辅因子操纵探索了铜绿假单胞菌接种 MFC 中的 EPT 改善。通过过表达 nadE(NAD 合成酶基因),细胞内辅因子池(NAD(H/(+)))的可用性显著增加,比原始菌株提供约三倍的更高功率输出(从 10.86 μW/cm(2)增加到 40.13 μW/cm(2))。与原始菌株相比,nadE 过表达菌株的电荷转移电阻降低了约一倍,电化学活性更高,这应该是功率输出提高的基础。此外,循环伏安法、HPLC 和 LC-MS 分析表明,过表达 nadE 后电子穿梭体(绿脓菌素)的浓度增加了约 1.5 倍,这是增强电化学活性的原因。因此,结果证实,细胞内辅因子的操纵可以是提高 MFCs 的 EPT 的有效方法,并暗示代谢工程在提高 EPT 方面具有很大的潜力。

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