Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coli

Microbial electrosynthesis (MES) or electro-fermentation (EF) is a promising microbial electrochemical technology for the synthesis of valuable chemicals or high-value fuels with aid of microbial cells as catalysts. By introducing electrical energy (current), fermentation environments can be altered...

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Main Authors: Jiao Feng, Qiuhao Lu, Kang Li, Sheng Xu, Xin Wang, Kequan Chen, Pingkai Ouyang
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fbioe.2020.590667/full
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author Jiao Feng
Qiuhao Lu
Kang Li
Sheng Xu
Xin Wang
Kequan Chen
Pingkai Ouyang
author_facet Jiao Feng
Qiuhao Lu
Kang Li
Sheng Xu
Xin Wang
Kequan Chen
Pingkai Ouyang
author_sort Jiao Feng
collection DOAJ
description Microbial electrosynthesis (MES) or electro-fermentation (EF) is a promising microbial electrochemical technology for the synthesis of valuable chemicals or high-value fuels with aid of microbial cells as catalysts. By introducing electrical energy (current), fermentation environments can be altered or controlled in which the microbial cells are affected. The key role for electrical energy is to supply electrons to microbial metabolism. To realize electricity utility, a process termed inward extracellular electron transfer (EET) is necessary, and its efficiency is crucial to bioelectrochemical systems. The use of electron mediators was one of the main ways to realize electron transfer and improve EET efficiency. To break through some limitation of exogenous electron mediators, we introduced the phenazine-1-carboxylic acid (PCA) pathway from Pseudomonas aeruginosa PAO1 into Escherichia coli. The engineered E. coli facilitated reduction of fumarate by using PCA as endogenous electron mediator driven by electricity. Furthermore, the heterologously expressed PCA pathway in E. coli led to better EET efficiency and a strong metabolic shift to greater production of reduced metabolites, but lower biomass in the system. Then, we found that synthesis of adenosine triphosphate (ATP), as the “energy currency” in metabolism, was also affected. The reduction of menaquinon was demonstrated as one of the key reactions in self-excreted PCA-mediated succinate electrosynthesis. This study demonstrates the feasibility of electron transfer between the electrode and E. coli cells using heterologous self-excreted PCA as an electron transfer mediator in a bioelectrochemical system and lays a foundation for subsequent optimization.
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spelling doaj.art-b47f0600df20439a9089e09ee2421ad72022-12-21T23:57:47ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852020-10-01810.3389/fbioe.2020.590667590667Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coliJiao FengQiuhao LuKang LiSheng XuXin WangKequan ChenPingkai OuyangMicrobial electrosynthesis (MES) or electro-fermentation (EF) is a promising microbial electrochemical technology for the synthesis of valuable chemicals or high-value fuels with aid of microbial cells as catalysts. By introducing electrical energy (current), fermentation environments can be altered or controlled in which the microbial cells are affected. The key role for electrical energy is to supply electrons to microbial metabolism. To realize electricity utility, a process termed inward extracellular electron transfer (EET) is necessary, and its efficiency is crucial to bioelectrochemical systems. The use of electron mediators was one of the main ways to realize electron transfer and improve EET efficiency. To break through some limitation of exogenous electron mediators, we introduced the phenazine-1-carboxylic acid (PCA) pathway from Pseudomonas aeruginosa PAO1 into Escherichia coli. The engineered E. coli facilitated reduction of fumarate by using PCA as endogenous electron mediator driven by electricity. Furthermore, the heterologously expressed PCA pathway in E. coli led to better EET efficiency and a strong metabolic shift to greater production of reduced metabolites, but lower biomass in the system. Then, we found that synthesis of adenosine triphosphate (ATP), as the “energy currency” in metabolism, was also affected. The reduction of menaquinon was demonstrated as one of the key reactions in self-excreted PCA-mediated succinate electrosynthesis. This study demonstrates the feasibility of electron transfer between the electrode and E. coli cells using heterologous self-excreted PCA as an electron transfer mediator in a bioelectrochemical system and lays a foundation for subsequent optimization.https://www.frontiersin.org/article/10.3389/fbioe.2020.590667/fullelectron transfer mediatorphenazine-1-carboxylic acidEscherichia colibioelectrocatalysissuccinate electrosynthesis
spellingShingle Jiao Feng
Qiuhao Lu
Kang Li
Sheng Xu
Xin Wang
Kequan Chen
Pingkai Ouyang
Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coli
Frontiers in Bioengineering and Biotechnology
electron transfer mediator
phenazine-1-carboxylic acid
Escherichia coli
bioelectrocatalysis
succinate electrosynthesis
title Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coli
title_full Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coli
title_fullStr Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coli
title_full_unstemmed Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coli
title_short Construction of an Electron Transfer Mediator Pathway for Bioelectrosynthesis by Escherichia coli
title_sort construction of an electron transfer mediator pathway for bioelectrosynthesis by escherichia coli
topic electron transfer mediator
phenazine-1-carboxylic acid
Escherichia coli
bioelectrocatalysis
succinate electrosynthesis
url https://www.frontiersin.org/article/10.3389/fbioe.2020.590667/full
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