Enhancing the Performance of Microbial Fuel Cells via Metabolic Engineering of Escherichia coli for Phenazine Production

Abstract

One of the central roles in the design, development, and application advances in mediator-based microbial electrochemical systems, such as microbial fuel cells (MFCs), is the establishment of efficient and successful communication between conductive electrode surfaces and microorganisms via modes of extracellular electron transfer (EET). Most microbial-based systems require the use of artificial electroactive mediators in order to facilitate and/or enhance electron transfer. Our previous work established an exogenous phenazine-based library as a mediator system to enable EET from the model microorganism Escherichia coli as a promising biotechnological host. However, the addition of exogenous mediators to a microbial electrochemical system has certain limiting downsides, specifically with regard to mediator toxicity to cells and increased operational expenses. Herein, we demonstrate the metabolic and genetic engineering of E. coli to self-generate phenazine metabolites endogenously by introducing the phenazine biosynthetic pathway from P. aeruginosa into E. coli. This biosynthetic pathway contains a phenazine cluster of seven genes, namely, phzABCDEFG (phzA-G), responsible for the synthetic conversion of phenazine-1-carboxylic acid (PCA) from chorismic acid, and two additional phenazine accessory genes phzM and phzS to catalyze the transformation of PCA to pyocyanin (PYO). We present the characterization of the engineered E. coli cells that were collected via electrochemical measurements, RNA sequencing, and microscopy imaging. Finally, the engineered E. coli cells were used for the design of a microbial fuel cell with enhanced performances, demonstrating a maximum power density increase from 127 ± 5 mW m −2 with nonengineered E. coli cells to 806 ± 7 mW m −2 with genetically engineered, phenazine-producing E. coli. Our results indicate that the introduction of a heterologous electron shuttle into E. coli is not only an efficient, but also a promising strategy toward establishing efficacious electron mediation in living bioelectrochemical systems and enhancing the overall MFC performance related to the MFC current generation and power output.

Combined electrical-electrochemical phenotypic profiling of antibiotic susceptibility of in vitro biofilm models

“…Gram-negative E. coli is one of the leading pathogens causing urinary tract, blood-stream, and many other infections in humans. Because E. coli is a well-known non-exoelectrogenic species, 68 the MFC with E. coli will not generate any meaningful electrical outputs while the EIS will be the main monitoring technique. Finally, Gram-positive Staphylococcus aureus is one of the most infectious pathogens, causing a wide range of clinical diseases.…”

Efficient Enhancement of Extracellular Electron Transfer in Shewanella oneidensis MR-1 via CRISPR-Mediated Transposase Technology

“…Furthermore, the synthesis of PCA was observed to significantly improve the startup speed of MFCs under experimental conditions. This improvement may be attributed to PCA serving as an easily diffusible electron mediator, rapidly facilitating electron transfer in the battery system …”

Effect of Glucose and Methylene Blue in Microbial Fuel Cells Using E. coli

“…The experimental evidence gathered here opens the doors to explore new applications of E. coli through genetic engineering. For instance, enhancing its electrogenic capacity through the production of endogenous redox mediators [58], direct electron transfer [59], or its ability to form a dense biofilm on the anode surface [20] are strategies that have recently begun to be evaluated. These strategies could further improve the performance of the MFC to achieve large-scale utilization of these devices.…”