Extracellular Electron Transfer Research Articles

Bio-Coated Graphitic Carbon Nitrides for Enhanced Nitrobenzene Degradation: Roles of Extracellular Electron Transfer

Graphitic carbon nitrides (g-C3N4) and microorganisms could collaboratively enhance photocatalytic properties or facilitate environmental depollution through coupled photocatalytic and biological reactions, which prevented the destruction of photocatalytic stresses to ecological systems and resulted in a sustainable technology for water remediation in rivers and lakes. However, the roles of bio-substances as well as electronic interactions between inorganic and organic systems were still unclear. Herein, g-C3N4, nitrogen-deficient g-C3N4 (ND-g-C3N4), and fluorinated g-C3N4 (F-g-C3N4) were coated with representative bacteria, i.e., Escherichia coli MG 1655, and characterized using integrated spectroscopic techniques. Photocatalytic activities were then evaluated through nitrobenzene degradation performance in an aqueous solution under visible light illumination. Nano-photocatalysts were observed to be adsorbed onto bio-aggregates, and surface hydrophilicity was convinced to be determined in the toxicity of photocatalysts in dark environments. Layered structures of ND-g-C3N4 and F-g-C3N4 were revealed in XRD spectra, and surface coverage of the Luria–Bertani medium was eliminated during E. coli cultivation. Hetero-junctions between photocatalysts and bio-substances were indicated in XPS results. Red-shifts for g-C3N4 and F-g-C3N4 materials as well as a slight blue-shift for ND-g-C3N4 were demonstrated in UV-vis spectra, which might be attributed to the destruction of nitrogen defects on ND-g-C3N4. Owing to the attached bio-substances, nitrobenzene removal could reach twice that with pristine photocatalysts, and ROS quantitative analysis confirmed that hydroxyl radicals were the determined reactive species degrading nitrobenzene in the water solution. The observation of more OH species generation indicated that extracellular electron transfer of E. coli reduced electron–hole recombination and provided reduction sites during photocatalytic degradation of nitrobenzene. This work proved additional electron-transfer paths and reaction mechanisms in hybridized photocatalytic and biological processes, which indicated that bio-activities could be a great promoter of material modification and the incorporation between inorganic and organic systems successfully showed an eco-friendly and sustainable pathway to utilize photocatalysts in natural water.

Conductive proteins‐based extracellular electron transfer of electroactive microorganisms

AbstractElectroactive microorganisms (EAMs) could utilize extracellular electron transfer (EET) pathways to exchange electrons and energy with their external surroundings. Conductive cytochrome proteins and nanowires play crucial roles in controlling electron transfer rate from cytosol to extracellular electrode. Many previous studies elucidated how the c‐type cytochrome proteins and conductive nanowires are synthesized, assembled, and engineered to manipulate the EET rate, and quantified the kinetic processes of electron generation and EET. Here, we firstly overview the electron transfer pathways of EAMs and quantify the kinetic parameters that dictating intracellular electron production and EET. Secondly, we systematically review the structure, conductivity mechanisms, and engineering strategies to manipulate conductive cytochromes and nanowire in EAMs. Lastly, we outlook potential directions for future research in cytochromes and conductive nanowires for enhanced electron transfer. This article reviews the quantitative kinetics of intracellular electron production and EET, and the contribution of engineered c‐type cytochromes and conductive nanowire in enhancing the EET rate, which lay the foundation for enhancing electron transfer capacity of EAMs.

2D covalent organic framework/reduced graphene oxide hybrid hydrogel for simultaneous power generation and organic contamination degradation in microbial fuel cell

Microbial fuel cells (MFCs) are promising devices that convert chemical energy into electrical energy via extracellular electron transfer between bacteria and electrodes. However, inefficient extracellular electron transfers and bacteria/electrode interactions often limit their performance. Herein, we demonstrate a hybrid hydrogel assembled by a 2D covalent organic framework (COF) and reduced graphene oxide (rGO) nanosheets as anode materials for MFCs. The 2D COF nanosheets effectively prevent the stacking of rGO nanosheets, resulting in the hybrid hydrogel with a high specific surface area (313.2 m2/g), abundant mesopores and macropores, and high electrical conductivity (492 S/m). The COF material also brings many quinone groups as redox mediators to facilitate electron transfer between bacteria and electrodes. The COF/rGO hybrid hydrogel enhances the growth of Shewanella decolorationis S12 cells, even under the influence of different organic dyes. Dense biofilms are formed on the hybrid hydrogel's surface and inside its macropores, further improving extracellular electron transfers. Assembled MFCs using COF/rGO anodes deliver a maximum power density of 905.1 mW/m2 and can operate for 600 h. They also enable simultaneous power generation and fast organic contamination degradation in electrolytes. This work shows the potential of using 2D nanoarchitectures to promote high-performance MFCs.

Extracellular electron uptake from a cathode by the lactic acid bacterium Lactiplantibacillus plantarum

A subset of microorganisms that perform respiration can endogenously utilize insoluble electron donors, such as Fe(II) or a cathode, in a process called extracellular electron transfer (EET). However, it is unknown whether similar endogenous EET can be performed by primarily fermentative species like lactic acid bacteria. We report for the first time electron uptake from a cathode by Lactiplantibacillus plantarum, a primarily fermentative bacteria found in the gut of mammals and in fermented foods. L. plantarum consumed electrons from a cathode and coupled this oxidation to the reduction of both an endogenous organic (pyruvate) and an exogenous inorganic electron acceptor (nitrate). This electron uptake from a cathode reroutes glucose fermentation toward lactate degradation and provides cells with a higher viability upon sugar exhaustion. Moreover, the associated genes and cofactors indicate that this activity is mechanistically different from that one employed by lactic acid bacteria to reduce an anode and to perform respiration. Our results expand our knowledge of the diversity of electroactive species and of the metabolic and bioenergetic strategies used by lactic acid bacteria.

Mediating the performance of anaerobic granular sludge by exogenous flavin supplementation: Flavin binding capacity and behavior, interspecies electron transfer, and methane production

Although flavins are known as effective electron mediators, the binding capacity of exogenous flavins by anaerobic granular sludge (AGS) and their role in interspecies electron transfer (IET) remains unknown. In this study, AGS was mediated by using three exogenous flavins of riboflavin (RF), flavin mononucleotide (FMN), and flavin adenine dinucleotide (FAD). Results showed that the total amounts of flavins associated with extracellular polymeric substance (EPS) of AGS increased by 2.03–2.42 and 3.83–4.94 folds, after exposure to 50 and 200 μM of exogenous flavins, respectively. A large portion of FMN and FAD was transformed into RF by AGS. Exogenous flavin mediation also stimulated the production of EPS and cytochrome c (c-Cyts) as well as cytochrome-bound flavins. The increased abundance of these electron mediators led to a reduced electrochemical impedance of EPS and improved extracellular electron transfer capacity. The methane production of AGS after mediation with exogenous RF, FMN, and FAD increased by 19.03–31.71%, 22.86–26.04%, and 28.51–33.44%, respectively. This study sheds new light on the role of exogenous flavins in promoting the IET process of a complex microbial aggregate of AGS.

Transcriptome Analysis Reveals the Inhibitory Effect of Cu2+ on Polyferric Sulfate Floc Reduction by Shewanella putrefaciens CN32.

Polyferric sulfate (PFS), an economical coagulant widely used for removing heavy metal contaminants from water, is susceptible to reduction and transformation by iron-reducing bacteria prevalent in sediments. However, the effect of heavy metal ions adsorbed in PFS flocs on this biological process remains unclear. According to our results, compared with other heavy metal cations (e.g., Cu2+, Cd2+, Zn2+, Ni2+, Pb2+, and Co2+), Cu2+ had a stronger inhibitory effect on PFS floc reduction by Shewanella putrefaciens CN32, a typical dissimilatory iron-reducing bacterium. The presence of Cu2+ remarkably influenced the global transcription of CN32, resulting in 782 upregulated genes and 713 downregulated genes that are mainly annotated in energy production, amino acid metabolism, protein biosynthesis, and oxidation‒reduction processes. The anaerobic TCA cycle for energy (electron) production was significantly activated in the presence of Cu2+, while the transcription of many genes related to the extracellular electron transfer pathway was downregulated, which is responsible for the decreased Fe3+ reduction. Moreover, the pathways of assimilatory sulfate reduction and subsequent cysteine biosynthesis were significantly enriched, which is hypothesized to result in the consumption of abundant energy produced from the enhanced anaerobic TCA cycle, revealing a strategy to address the oxidative stress caused by Cu2+. This work elucidates the unusual suppressive effects of Cu2+ on the microbial reduction of PFS flocs, which reveals the high resistance of PFS flocs to microbial destruction when used to treat Cu2+ pollution in water, thus demonstrating their tremendous practical prospects.

Extracellular electron transfer for aerobic denitrification mediated by the bioelectric catalytic system with zero-carbon source

The slow rate of electron transfer and the large consumption of carbon sources are technical bottlenecks in the biological treatment of wastewater. Here, we first proposed to domesticate aerobic denitrifying bacteria (ADB) from heterotrophic to autotrophic by electricity (0.6 V) under zero organic carbon source conditions, to accelerate electron transfer and shorten hydraulic retention time (HRT) while increasing the biodegradation rate. Then we investigated the extracellular electron transfer (EET) mechanism mediated by this process, and additionally examined the integrated nitrogen removal efficiency of this system with composite pollution. It was demonstrated that compared with the traditional membrane bioreactor (MBR), the BEC displayed higher nitrogen removal efficiency. Especially at C/N = 0, the BEC exhibited a NO3--N removal rate of 95.42 ± 2.71 % for 4 h, which was about 6.5 times higher than that of the MBR. Under the compound pollution condition, the BEC still maintained high NO3--N and tetracycline removal (94.52 ± 2.01 % and 91.50 ± 0.001 %), greatly superior to the MBR (10.64 ± 2.01 % and 12.00 ± 0.019 %). In addition, in-situ electrochemical tests showed that the nitrate in the BEC could be directly converted to N2 by reduction using electrons from the cathode, which was successfully demonstrated as a terminal electron acceptor.

Ex-situ electrochemical characterisation of fixed-bed denitrification biocathodes: A promising strategy to improve bioelectrochemical denitrification

The worldwide issue of nitrate-contaminated groundwater requires practical solutions, and electro-bioremediation offers a promising and sustainable treatment. While it has shown potential benefits, there is room for improvement in treatment rates, which is crucial for its further and effective implementation. In this field, electrochemical characterisation is a valuable tool for providing the foundation for optimising bioelectrochemical reactors, but applying it in fixed-bed reactors is challenging due to its high intrinsic electrical resistance. To overcome these challenges, this study employed the easy and swift eClamp methodology to screen different process parameters and their influence on the performance of fixed-bed denitrifying biocathodes composed of granular graphite. Granules were extracted and studied ex-situ under controlled conditions while varying key operational parameters (such as pH, temperature, and nitrate concentration). In the studied biocathode, the extracellular electron transfer associated with denitrification was identified as the primary limiting step with a formal potential of −0.225 ± 0.007 V vs. Ag/AgCl sat. KCl at pH 7 and 25 °C. By varying the nitrate concentration, it was revealed that the biocathode exhibits a strong affinity for nitrate (KMapp of 0.7 ± 0.2 mg N–NO3− L−1). The maximum denitrification rate was observed at a pH of 6 and a temperature of 35 °C. Furthermore, the findings highlight a 2e−/1H+ transfer, which holds considerable implications for the energy metabolism of bioelectrochemical denitrifiers. These compiled results provide valuable insights into the understanding of denitrifying biocathodes and enable the improvement and prediction of their performance.

Enhancing biocathode denitrification performance with nano-Fe3O4 under polarity period reversal

The presence of excessive concentrations of nitrate poses a threat to both the environment and human health, and the bioelectrochemical systems (BESs) are attractive green technologies for nitrate removal. However, the denitrification efficiency in the BESs is still limited by slow biofilm formation and nitrate removal. In this work, we demonstrate the efficacy of novel combination of magnetite nanoparticles (nano-Fe3O4) with the anode-cathode polarity period reversal (PPR-Fe3O4) for improving the performance of BESs. After only two-week cultivation, the highest cathodic current density (7.71 ± 1.01 A m−2) and NO3−-N removal rate (8.19 ± 0.97 g m−2 d−1) reported to date were obtained in the PPR-Fe3O4 process (i.e., polarity period reversal with nano-Fe3O4 added) at applied working voltage of −0.2 and −0.5 V (vs Ag/AgCl) under bioanodic and biocathodic conditions, respectively. Compared with the polarity reversal once only process, the PPR process (i.e., polarity period reversal in the absence of nano-Fe3O4) enhanced bioelectroactivity through increasing biofilm biomass and altering microbial community structure. Nano-Fe3O4 could enhance extracellular electron transfer as a result of promoting the formation of extracellular polymers containing Fe3O4 and reducing charge transfer resistance of bioelectrodes. This work develops a novel biocathode denitrification strategy to achieve efficient nitrate removal after rapid cultivation.

Enhanced performance of microbial fuel cells using electrochemically treated carbon felt anode

The microbial fuel cell (MFC) technology is emerging as an effective technology for wastewater treatment to remove and detect many pollutants and simultaneously generate power. The anode is an essential component for bacterial attachment and extracellular electron transfer (EET). Thus, anode performance is critical for improving an MFC system's overall performance. Materials that are electronically conductive and provide favorable conditions for creating biofilm are good candidates for the anode. Carbon paper and carbon felt are the most used anode materials. However, the characteristics of these materials can be modified to increase their performance. This paper presents a modification of the conventional carbon anode by electrolyzing the carbon felt in a phosphate buffer and an experimental evaluation of the impact of the treatment. The tests were performed using an air cathode MFC, electrogenic bacteria Shewanella Baltica 20 fed on lactose-rich L-B. The treatment with phosphate buffer generates functional groups on the surface of the carbon felt, which establishes robust biofilm on the anode and offers lower charge-transfer resistance compared to the untreated carbon felt. This facilitates electron transfer from exoelectrogens to the anode, increasing the current density and power density output. Three times higher power density was observed in the cell with a modified anode than in an untreated carbon-felt anode.

The influencing mechanism of AD-MEC domesticated sludge to alleviates propionate accumulation and enhances methanogenesis

Anaerobic digestion combined with microbial electrolysis cell (AD-MEC) could maintain stable reactor operation and alleviating the anaerobic digestion (AD) propionate accumulation. In this study, the addition of sludge to AD-MEC was examined as a way to enhance system performance and explore the microbial interaction mechanism after electric field domestication. The results showed that under 1000 and 4000 mg/L propionate, the methane production of the sludge from AD-MEC increased by 34.29 % and 9.70 %, respectively, as compared to the AD sludge. Gompertz fitting analysis showed that sludge after electric field domestication enhancing its continuous methanogenic capacity. Further analysis showed that sludge extracellular electron transfer capacity was enhanced in AD-MEC and that its domesticated granular sludge formed a microbial community function with acid-degrading synergistic methanogenesis. The results of the study may provide theoretical support and optimization strategies for the application of AD-MEC system.

Cathode materials in microbial electrosynthesis systems for carbon dioxide reduction: recent progress and perspectives

Microbial electrosynthesis (MES) is an emerging technology that enables the synthesis of value-added chemicals from carbon dioxide (CO2) or inorganic carbon compounds by coupling renewable electricity to microbial metabolism. However, MES still faces challenges in achieving high production of value-added chemicals due to the limited extracellular electron transfer efficiency at the biotic-abiotic interfaces. To overcome this bottleneck, it is crucial to develop novel cathodes and modified materials. This review systematically summarizes recent advancements in cathode materials in the field of electrocatalyst-assisted and photocatalyst-assisted MES. The effects of various material types are further investigated by comparing metal-free and metal materials and photocatalyst materials of different semiconductor types. Additionally, the review introduces the maximum production rate of value-added chemicals and conversion efficiency achieved by these cathode materials while highlighting the advantages and disadvantages of different material types. To the best of our knowledge, in electrocatalyst-assisted systems, the maximum CH4 yield on graphene aerogel/polypyrrole cathode achieved 1,672 mmol m-2 d-1, and the maximum Faraday efficiency (FE) of CH4 reached up to 97.5% on graphite plate. Meanwhile, the maximum acetate yield achieved 1,330 g m-2 d-1 with CO2 conversion efficiency into acetate close to 100% on carbon nanotube cathodes. In photocatalyst-assisted systems, the maximum acetate yield could reach 0.51 g L-1 d-1 with the coulombic efficiency of 96% on the MnFe2O4/g-C3N4 photocathode. Finally, prospects for future development and practical applications of MES are discussed, offering theoretical guidance for the fabrication of cathode materials that can improve production efficiency and reduce energy input.

Percolation-Modeling Comparison Between the Conductivities of Zinc-Graphene Quantum Dot Nanocomposite and Graphite during Extracellular Electron Transfer in Microbial Fuel Cell Electrodes

Percolation-Modeling Comparison Between the Conductivities of Zinc-Graphene Quantum Dot Nanocomposite and Graphite during Extracellular Electron Transfer in Microbial Fuel Cell Electrodes

Influence of shear stress on electroactive biofilm characteristics and performance in microbial fuel cells

This study has provided comprehensive insights into the intricate relationship between shear stress and the development, structure, and functionality of electroactive biofilms in Microbial Fuel Cells (MFCs). A multichannel microfluidic MFC reactors that created specific shear stress on the anode, were designed for the simultaneous study of multiple flow conditions using the same medium. Then, the evolution of the biofilm growth under different shear stress conditions (1, 5 and 10 mPa) were compared. The taxonomic and functional structure was studied by 16S rRNA gene and metagenomic sequencing and the physical biofilm characteristics were measured via fluorescence microscopy. The results demonstrate the pivotal role of shear stress in influencing the growth kinetics, electrical performance, and physical structure of anodic biofilms. Notably, the selection of specific EAB was observed to be shear stress-dependent, with a marked increase in specific EAB abundance as shear stress increased. The power density, while not directly correlated with the relative abundance of specific or nonspecific EAB, exhibited a strong linear relationship with biofilm coverage. This suggests that factors beyond the microbial composition, potentially including mass transport or electrochemical conditions, might be instrumental in determining electricity production. The functional metagenomic analysis further highlighted the complexities of extracellular electron transfer (EET) mechanisms in electroactive biofilm. While certain genes associated with EET in known species such as Geobacter and Shewanella were identified, the study also examined the limitations of solely relying on genetic markers to infer EET capabilities, emphasizing the need for complementary metaproteomic analyses. This study demonstrates the multifaceted impact of shear stress on electroactive biofilm and paves the way for future investigations aimed at harnessing the potential of electroactive biofilms in microbial fuel cell applications.

Filamentous marine Gram-positive Nocardiopsis dassonvillei biofilm as biocathode and its electron transfer mechanism

This study investigated electrochemical characteristics of Gram-positive, Nocardiopsis dassonvillei B17 facultative bacterium in bioelectrochemical systems. The results demonstrated that anodic and cathodic reaction rates were catalyzed by this bacterium, especially by utilization of aluminium alloy as a substrate. Cyclic voltammogram results depicted an increase of peak current and surface area through biofilm development, confirming its importance on catalysis of redox reactions. Phenazine derivatives were detected and their electron mediating behavior was evaluated exogenously. A symmetrical redox peak in the range of −59 to −159 mV/SHE was observed in cyclic voltammogram of bacterial solution supplemented with 12 μM phenazine, a result consistent with cyclic voltammogram of a 5-d biofilm, confirming its importance as an electron mediator in extracellular electron transfer. Furthermore, the dependency of bacterial catalysis and polarization potential were studied. These results suggested that B17 biofilm behaved as a biocathode and transferred electrons to bacterial cells through a mechanism associated with electron mediators.

Enhancing extracellular electron transfer and power generation in microbial fuel cell using a ferrocene-based conjugated oligoelectrolyte

The anode compartment, as an electron generation station, determines the power performance and contaminant removal in microbial fuel cell (MFC). However, the extracellular electron transfer (EET) process limits bioelectricity generation. In this work, the role of conjugated oligoelectrolytes (COEs) on catalyzing bacterial activity toward bio-current production was investigated. In this regard, two COEs, namely [4-[1-(3-methylimidazolium chloride)]butyl] ferrocene (MIF+) and Bis [4-[1-(3-methylimidazolium chloride)]butyl] ferrocene (BMIF+) were synthesized and the increases in anodic current output were probed through MFC device. The electrochemical analyses revealed excellent performance in bio-current production for BMIF+ stained cells. The tolerance threshold of COEs stained cells for different concentrations of COEs was investigated using chronoamperometry (CA) test. Additionally, the power performance of MFC exhibited the highest value of 115.46 mW m−2 for the BMIF+ stained cells in comparison with MIF+ stained cells (73.12 mW m−2) and unstained cells (25.8 mW m−2). The results demonstrated that spiking cells' membranes with COEs is a meaningful strategy to facilitate the EET process and produce bioelectricity.

Metaproteomic and Metagenomic-Coupled Approach to Investigate Microbial Response to Electrochemical Conditions in Microbial Fuel Cells.

MFCs represent a promising sustainable biotechnology that enables the direct conversion of organic matter from wastewater into electricity using bacterial biofilms as biocatalysts. A crucial aspect of MFCs is how electroactive bacteria (EAB) behave and their associated mechanisms during extracellular electron transfer to the anode. A critical phase in the MFC start-up process is the initial colonization of the anode by EAB. Two MFCs were operated with an external resistance of 1000 ohms, one with an applied electrical voltage of 500 mV during the initial four days of biofilm formation and the other without any additional applied voltage. After stabilization of electricity production, total DNA and protein were extracted and sequenced from both setups. The combined metaproteomic/metagenomic analysis revealed that the application of voltage during the colonization step predominantly increased direct electron transfer via cytochrome c, mediated primarily by Geobacter sp. Conversely, the absence of applied voltage during colonization resulted in a broader diversity of bacteria, including Pseudomonas and Aeromonas, which participated in electricity production via mediated electron transfer involving flavin family members.

Optimizing the Metal Bioreduction Process in Recombinant Shewanella azerbaijanica Bacteria: A Novel Approach via mtrC Gene Cloning and Nitrate-Reducing Pathway Destruction.

Environmental pollution is growing every day in terms of the increase in population, industrialization, and urbanization. Shewanella azerbaijanica is introduced as a highly potent bacterium in metal bioremediation. The mtrC gene was selected as a cloning target to improve electron flux chains in the EET (extracellular electron transfer) pathway. Using the SDM (site-directed mutagenesis) technique, the unique gene assembly featured the mtrC gene sandwiched between two napD/B genes to disrupt the nitrate reduction pathway, which serves as the primary metal reduction competitor. Shew-mtrC gene construction was transferred to expression plasmid pET28a (+) in the expression host bacteria (E. coli BL21 and S. azerbaijanica), in pUC57, cloning plasmid, which was transferred to the cloning host bacteria E. coli Top10 and S. azerbaijanica. All cloning procedures (i.e., synthesis, insertion, transformation, cloning, and protein expression) were verified and confirmed by precise tests. ATR-FTIR analysis, CD, western blotting, affinity chromatography, SDS-PAGE, and other techniques were used to confirm the expression and structure of the MtrC protein. The genome sequence and primers were designed according to the submitted Shewanella oneidensisMR-1 genome, the most similar bacteria to this native species. The performance of recombinant S. azerbaijanica bacterium in metal bioremediation, as sustainable strategy, has to be verified by more research.

Bi-directional regulation of electroactive microbial community using Au/antimicrobial peptide nanocomposite

The power generation and pollutants removal efficiencies of mixed electroactive microbial community rely on the effective electron transfer between outer membrane proteins of electroactive electricigens. However, the poor conductivity of protein and various non-electrogenic bacteria greatly hinder the electron transfer and effective contact between electricigens. Herein, we report a novel “bi-directional” microbial community regulation method that can selectively inhibit Gram-positive non-electrogenic bacteria and enhances the conductivity and electron transfer between electrogenic bacteria and the electrode in MFC by taking the advantages of the excellent conductive and bacteriostatic properties of Au/Nisin nanocomposite. The Au/Nisin stimulation endows microbial fuel cell (MFC) a high-efficiency functional community, which increases the power density and decolorization rate by 103 % and 33 %, respectively. The high conductivity, and selectivity and antimicrobial activity of the nanocomposite improve the electrochemical activity of the bioanode, hereby promoting the microbial extracellular electron transfer and increasing the proportion of electrogenic bacteria such as Proteobacteria, Bacteroidetes and Desulfovibrio in the biofilm. Our work successfully demonstrates that the construction of multifunctional metallic peptide nanocomposite can effectively regulate microbial community to improve the electrochemical performance of MFC.

Effects of plasticizer on removal of antibiotics and antibiotic resistance genes from agricultural soils via soil microbial fuel cells

Soil microbial fuel cells (MFCs), a novel ecosystem technology, have recently been intensively studied for antibiotic-polluted soils. However, actual agricultural soils are always contaminated by mixed pollutants, especially plasticizers from extensively used agricultural plastic films. The aim of this study is to investigate the effect of di-2-ethylhexyl phthalate (DEHP, a representative plasticizer in soil) on the removal of sulfadiazine (SDZ, a frequently detected antibiotic in natural environments), antibiotic resistance genes (ARGs), and the microbial community in soil MFCs. Our results confirmed that soil MFCs maintained a good antibiotic removal ability even under the influence of residual DEHP and achieved a higher removal performance at higher DEHP concentrations due to enhanced power generation. Specifically, a higher DEHP concentration had a favorable effect on antibiotic removal in soil MFCs because the biodegradation efficiency was improved in both the upper (i.e., to 0.268 ± 0.021 mg kg−1 from 4.867 ± 0.221 mg kg−1) and lower layers (i.e., to 0.293 ± 0.047 mg kg−1 from 4.867 ± 0.221 mg kg−1) of polluted soils. Moreover, a high DEHP concentration significantly promoted the abundance of bacteria associated with electricity generation compared with a lower DEHP concentration, resulting in the promotion of extracellular electron transfer, and enhancing SDZ degradation. The increased ARG abundance may have been caused by the enrichment of ARG potential hosts brought about by high DEHP concentrations, likely due to the increased conjugative transfer rates of the RP4 plasmid due to decreased membrane permeability and an increased reactive oxygen species content. The results revealed the ecological risk of residual DEHP in soil that promotes ARG transmission in soil MFCs, although it has the potential to reduce SDZ toxicity through horizontal gene transfer. We also highlight concerns regarding the management of antibiotics and plasticizers in soil. The negative effects of plasticizers on antibiotic removal should be carefully evaluated when using soil MFCs for the in situ remediation of antibiotic-contaminated soil.