Extracellular Electron Transfer Research Articles

Extracellular electron transfer explained

Extracellular electron transfer explained Arpita Bose, PhD from Washington University in St. Louis, guides us through host-associated impacts and biotechnological applications of extracellular electron transfer in electrochemically active bacteria. Electron flow and oxidative and reductive reactions, referred to as “redox reactions,” collectively impact the outcomes of biochemical pathways essential for cell growth, energy conservation, and stress response throughout various organisms. An example of these organisms is electrochemically active bacteria (EAB), which can link internal redox reactions with external electron acceptors or donors via a process known as extracellular electron transfer (EET).

Microbially Driven Iron Cycling Facilitates Organic Carbon Accrual in Decadal Biochar-Amended Soil.

Soil organic carbon (SOC) is pivotal for both agricultural activities and climate change mitigation, and biochar stands as a promising tool for bolstering SOC and curtailing soil carbon dioxide (CO2) emissions. However, the involvement of biochar in SOC dynamics and the underlying interactions among biochar, soil microbes, iron minerals, and fresh organic matter (FOM, such as plant debris) remain largely unknown, especially in agricultural soils after long-term biochar amendment. We therefore introduced FOM to soils with and without a decade-long history of biochar amendment, performed soil microcosm incubations, and evaluated carbon and iron dynamics as well as microbial properties. Biochar amendment resulted in 2-fold SOC accrual over a decade and attenuated FOM-induced CO2 emissions by approximately 11% during a 56-day incubation through diverse pathways. Notably, biochar facilitated microbially driven iron reduction and subsequent Fenton-like reactions, potentially having enhanced microbial extracellular electron transfer and the carbon use efficiency in the long run. Throughout iron cycling processes, physical protection by minerals could contribute to both microbial carbon accumulation and plant debris preservation, alongside direct adsorption and occlusion of SOC by biochar particles. Furthermore, soil slurry experiments, with sterilization and ferrous iron stimulation controls, confirmed the role of microbes in hydroxyl radical generation and biotic carbon sequestration in biochar-amended soils. Overall, our study sheds light on the intricate biotic and abiotic mechanisms governing carbon dynamics in long-term biochar-amended upland soils.

Fe0-to-microbe electron transfer corrosion of EH36 steel by planktonic cells of Desulfovibrio vulgaris mediated by riboflavin

This study investigated the Fe0-to-microbe extracellular electron transfer (EET) corrosion of EH36 steel by planktonic Desulfovibrio vulgaris cells using Tetrakis hydroxymethyl phosphonium sulfate (THPS), peptide E6, and riboflavin (RF) as tools. 60 min after 20 ppm THPS & E6 injection and 50 ppm THPS injection, there was no difference in sessile cell counts, but planktonic cell counts were different. The subsequent injection of 20 ppm RF accelerated D. vulgaris MIC in varying degrees within minutes. This was attributed to RF-mediated EET of planktonic cells to accelerate corrosion, which can be further confirmed by the elevated expression levels of cytochrome c.

Periplasmic electron transfer network in Geobacter sulfurreducens revealed by biomolecular interaction studies

AbstractMultiheme cytochromes located in different compartments are crucial for extracellular electron transfer in the bacterium Geobacter sulfurreducens to drive important environmental processes and biotechnological applications. Recent studies have unveiled that for particular sets of electron terminal acceptors, discrete respiratory pathways selectively recruit specific cytochromes from both the inner and outer membranes. However, such specificity was not observed for the abundant periplasmic cytochromes, namely the triheme cytochrome family PpcA‐E. In this work, the distinctive NMR spectroscopic signatures of these proteins in different redox states were explored to monitor pairwise interactions and electron transfer reactions between each pair of cytochromes. The results showed that the five proteins interact transiently and can exchange electrons between each other revealing intra‐promiscuity within the members of this family. This discovery is discussed in the light of the establishment of an effective electron transfer network by this pool of cytochromes. This network is advantageous to the bacteria as it enables the maintenance of the functional working potential redox range within the cells.

The dmsEFABGH operon encodes an essential and modular electron transfer pathway for extracellular iodate reduction by Shewanella oneidensis MR-1.

Extracellular iodate reduction by Shewanella spp. contributes to iodide generation in the biogeochemical cycling of iodine. However, there is a disagreement on whether Shewanella spp. use different extracellular electron transfer pathways with dependence on electron donors in iodate reduction. In this study, a series of gene deletion mutants of Shewanella oneidensis MR-1 were created to investigate the roles of dmsEFABGH, mtrCAB, and so4357-so4362 operons in iodate reduction. The iodate-reducing activity of the mutants was tested with lactate, formate, and H2 as the sole electron donors, respectively. In the absence of single-dms gene, iodate reduction efficiency of the mutants was only 12.9%-84.0% with lactate at 24 hours, 22.1%-85.9% with formate at 20 hours, and 19.6%-57.7% with H2 at 42 hours in comparison to complete reduction by the wild type. Progressive inhibition of iodate reduction was observed when the dms homolog from the so4357-so4362 operon was deleted in the single-dms gene mutants. This result revealed complementation of dmsEFABGH by so4357-so4362 at the single-gene level, indicating modularity of the extracellular electron transfer pathway encoded by dmsEFABGH operon. Under the conditions of all electron donors, significant inhibition of iodate reduction and accumulation of H2O2 were detected for ΔmtrCAB. Collectively, these results demonstrated that the dmsEFABGH operon encodes an essential and modular iodate-reducing pathway without electron donor dependence in S. oneidensis MR-1. The mtrCAB operon was involved in H2O2 elimination with all electron donors. The findings in this study improved the understanding of molecular mechanisms underlying extracellular iodate reduction.IMPORTANCEIodine is an essential trace element for human and animals. Recent studies revealed the contribution of microbial extracellular reduction of iodate in biogeochemical cycling of iodine. Multiple reduced substances can be utilized by microorganisms as energy source for iodate reduction. However, varied electron transfer pathways were proposed for iodate reduction with different electron donors in the model strain Shewanella oneidensis MR-1. Here, through a series of gene deletion and iodate reduction experiments, we discovered that the dmsEFABGH operon was essential for iodate reduction with at least three electron donors, including lactate, formate, and H2. The so4357-so4362 operon was first demonstrated to be capable of complementing the function of dmsEFABGH at single-gene level.

Electroactive Shewanella algae accelerates the crevice corrosion of X70 pipeline steel in marine environment

Crevice corrosion causes severe damage to metallic materials in marine environments. The inner mechanism of crevice corrosion in the presence of microbes deserves in-depth investigation. Herein, the electroactive Shewanella algae was found to accelerate the crevice corrosion of X70 pipeline steel through weight loss analysis, electrochemical tests, characterization of surface morphology, and analysis of corrosion products. The corrosion current increased to 2.3 μA cm−2, which was 2.3 folds of that in a sterile medium. Further electrochemical tests were carried out with exogenous addition of riboflavin. It confirmed that extracellular electron transfer accelerated the crevice corrosion in which S. algae participated.

Accelerating cell division of Shewanella oneidensis to promote extracellular electron transfer rate for efficient pollution treatment

The slow rate of extracellular electron transfer (EET) of electroactive microorganisms (EAMs) remains a predominate bottleneck that restricts practical applications of bio-electrochemical systems. Cell division has significant effects on cell cycle, morphology, growth and metabolism. However, the relation between cell division and the EET rate of Shewanella oneidensis has not been established. Here, we employed modular engineering strategy to accelerate DNA replication in the C period and divisome formation in the D period of cell cycle, which decreased cellular volume and enhanced the EET efficiency. Assembly of the C and D period modules further decreased the cell volume by 82.0 % and enhanced power density by 3.12-fold. Electrophysiological and transcriptomic analyses synergistically revealed that the programmed cell volume decrease facilitated lactate uptake and cellular metabolism due to the increased specific surface area (SSA), which consequently reinforced intracellular electron generation. Moreover, the reduced cell size facilitated electroactive biofilm formation. Finally, programmed increase in riboflavin biosynthesis and transport further strengthened indirect EET and boosted output power density to 1537.8 ± 116.9 mW m−2, 21.1-fold of that of the WT. The engineered strains exhibited superior abilities for Cr6+ reduction and azo dyes degradation. This study shed light on the underlying mechanism how reduced cell size impacts electrophysiology of EAMs, and indicated accelerating cell division is a promising avenue to increase the EET of EAMs for efficient environmental pollution treatment.

Analysis of the contribution of different electron transfer pathways for hydrogen production in a bioelectrochemically assisted dark fermentation system

This research analyzed the contribution of different electron transfer pathways for H2 production in a bioelectrochemicallly assisted dark fermentation system (BEDF), and compared to an electric field-driven dark fermentation (EFDF) reactor. The results showed that intrinsic extracellular electron transfer (iEET) via dark fermentation accounted for 76.3% of the H2 production in the BEDF reactor. In comparison, the extracellular electron transfer (bEET) pathway via the bioelectrode enhanced by the bioelectrochemical system and the electric field-driven extracellular electron transfer (eEET) in the bulk solution accounted for 5% and 18.7%, respectively. This suggests that the main electron transfer pathway for H2 production comes from the bulk solution rather than that on the bioelectrodes. Under the condition of electric field, extracellular polymeric substances (EPS) were secreted in large quantities in the bulk solution, and electroactive microorganisms such as Proteobacteria were significantly enriched, which further promote the H2 production through the eEET pathway.

Inoculum source determines the stress resistance of electroactive functional taxa in biofilms: A metagenomic perspective

The inoculum has a crucial impact on bioreactor initialization and performance. However, there is currently a lack of guidance on selecting appropriate inocula for applications in environmental biotechnology. In this study, we applied microbial electrolysis cells (MECs) as models to investigate the differences in the functional potential of electroactive microorganisms (EAMs) within anodic biofilms developed from four different inocula (natural or artificial), using shotgun metagenomic techniques. We specifically focused on extracellular electron transfer (EET) function and stress resistance, which affect the performance and stability of MECs. Community profiling revealed that the family Geobacteraceae was the key EAM taxon in all biofilms, with Geobacter as the dominant genus. The c-type cytochrome gene imcH showed universal importance for Geobacteraceae EET and was utilized as a marker gene to evaluate the EET potential of EAMs. Additionally, stress response functional genes were used to assess the stress resistance potential of Geobacter species. Comparative analysis of imcH gene abundance revealed that EAMs with comparable overall EET potential could be enriched from artificial and natural inocula (P > 0.05). However, quantification of stress response gene copy numbers in the genomes demonstrated that EAMs originating from natural inocula possessed superior stress resistance potential (196 vs. 163). Overall, this study provides novel perspectives on the inoculum effect in bioreactors and offers theoretical guidance for selecting inoculum in environmental engineering applications.

Regulatory mechanisms of biochar alleviating ammonia inhibition to methanogenesis during long-term operation of anaerobic membrane bioreactor treating swine wastewater

Anaerobic Membrane Bioreactor (AnMBR) is regarded as an advanced technology for the anaerobic digestion (AD) of swine wastewater. However, the high ammonia level in swine wastewater is a crucial issue to inhibit methane production. This study aimed to establish a biochar-assisted AnMBR (BC) to mitigate ammonia inhibition during AD of swine wastewater. As the gradual ammonia loading rate (ALR) increased from 3.0 g/L to 6.0 g/L, BC maintained methane yields ranging from 74.9 % to 48.1 %, which were 9.1 % to 33.3 % higher than those of a regular AnMBR (CT). Moreover, the COD removal efficiency steadily surpassed 80 %. Although the increase in ALR had negative effects on both BC and CT, the presence of biochar enhanced the methanogenic activity of bulk sludge, specifically accelerating processes involved in syntrophic acetate oxidation and CO2-reducing methanogenesis under high ALR conditions. Integrated characterizations using PARAFAC-based EPS analysis, INT-ETS, and WO3 probe-based extracellular electron transfer (EET) activities indicated that biochar stimulated the secretion of humic-like and aromatic protein-like compounds in the TB-EPS, which likely established a redox-active matrix with biochar between VFA oxidation bacteria and CO2-reducing methanogens to facilitate EET. This potentially made the syntrophic VFA oxidation with favorably thermodynamic kinetics under high ammonia stress. Furthermore, the analysis of microbial community coupling prediction of functional genes associated with methanogenic pathways revealed that as ALR increased, the presence of biochar re-shaped the microbial communities by enriching electro-active Syntrophomonas and Methanosarcina/Methanospirillum, which mainly triggering EET-based syntrophic methanogenesis by accelerating the intracellular enzymatic transformation from Formylmethanofuran to 5,10-Methylenetetrahydromethanopterin process. We expect the major findings of this study provide new insights to understand the mechanisms of biochar alleviating ammonia inhibition during long-term operation of AnMBR.

Acceleration mechanism of riboflavin on Fe0-to-microbe electron transfer in corrosion of EH36 steel by Pseudomonas aeruginosa

Riboflavin (RF), as a common electron mediator that can accelerate extracellular electron transfer (EET), is usually used as a probe to confirm EET-microbiologically influenced corrosion (MIC). However, the acceleration mechanism of RF on EET-MIC is still unclear, especially the effect on gene expression in bacteria. In this study, a 13-mer antimicrobial peptide E6 and tetrakis hydroxymethyl phosphonium sulfate (THPS) were used as new tools to investigate the acceleration mechanism of RF on Fe0-to-microbe EET in corrosion of EH36 steel caused by Pseudomonas aeruginosa. 60 min after 20 ppm (v/v) THPS and 20 ppm THPS & 100 nM E6 were injected into P. aeruginosa 1 and P. aeruginosa 2 (two glass bottles containing P. aeruginosa with different treatments) at the 3-d incubation, respectively, P. aeruginosa 1 and P. aeruginosa 2 had a similar planktonic cell count, whereas the sessile cell count in P. aeruginosa 1 was 1.3 log higher than that in P. aeruginosa 2. After the 3-d pre-growth and subsequent 7-d incubation, the addition of 20 ppm (w/w) RF increased the weight loss and maximum pit depth of EH36 steel in P. aeruginosa 1 by 0.7 mg cm−2 and 4.1 μm, respectively, while only increasing those in P. aeruginosa 2 by 0.4 mg cm−2 and 1.7 μm, respectively. This suggests that RF can be utilized by P. aeruginosa biofilms since the corrosion rate should be elevated by the same value if it only acts on the planktonic cells. Furthermore, the EET capacity of P. aeruginosa biofilm was enhanced by RF because the protein expression of cytochrome c (Cyt c) gene in sessile cells was significantly increased in the presence of RF, which accelerated EET-MIC by P. aeruginosa against EH36 steel.

Modulating anodic performance of halophilic electroactive microbial consortia with selective enrichment using metal-based terminal electron acceptors

Long start-up times and lack of robust halophilic electroactive microbes (EAM) challenge the implementation of microbial fuel cells (MFC) for treating saline wastewater. Here a pragmatic strategy is presented to selectively enrich halophilic EAM consortium capitalising on their cellular respiration process using graphene oxide (GO) and metal ions (Fe3+, Mn4+ and Cu2+) as the primary and secondary terminal electron acceptors (TEA), respectively. Enrichment of GO-respiring EAM consortium with Fe3+ ions enabled growth of an efficient anodic biofilm within a short start-up time of 50 h and generated up to 1.1 W/m3 while treating highly saline electrolyte (2 % NaCl). In conjunction with predictive genetic profiling, in-depth electrochemical analysis of the biofilm unravelled key mechanisms of direct extracellular electron transfer for generating high anodic currents. Additionally, the inclusion of Fe3+ ions as secondary TEA upregulated the metabolic activity of GO-respiring EAM, which subsequently influenced their anodic performance rather than the relative abundance of exoelectrogens in the biofilm. Thus, this study stimulates the discovery of novel EAM communities using an advanced and sensible design of selective media by varying the electron donor and TEA couplings.

Transcriptional regulation of living materials via extracellular electron transfer.

Engineered living materials combine the advantages of biological and synthetic systems by leveraging genetic and metabolic programming to control material-wide properties. Here, we demonstrate that extracellular electron transfer (EET), a microbial respiration process, can serve as a tunable bridge between live cell metabolism and synthetic material properties. In this system, EET flux from Shewanella oneidensis to a copper catalyst controls hydrogel cross-linking via two distinct chemistries to form living synthetic polymer networks. We first demonstrate that synthetic biology-inspired design rules derived from fluorescence parameterization can be applied toward EET-based regulation of polymer network mechanics. We then program transcriptional Boolean logic gates to govern EET gene expression, which enables design of computational polymer networks that mechanically respond to combinations of molecular inputs. Finally, we control fibroblast morphology using EET as a bridge for programmed material properties. Our results demonstrate how rational genetic circuit design can emulate physiological behavior in engineered living materials.

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

Electroactive bacteria, exemplified by Shewanella oneidensis MR-1, have garnered significant attention due to their unique extracellular electron-transfer (EET) capabilities, which are crucial for energy recovery and pollutant conversion. However, the practical application of MR-1 is constrained by its EET efficiency, a key limiting factor, due to the complexity of research methodologies and the challenges associated with the practical use of gene editing tools. To address this challenge, a novel gene integration system, INTEGRATE, was developed, utilizing CRISPR-mediated transposase technologies for precise genomic insertion within the S. oneidensis MR-1 genome. This system facilitated the insertion of extensive gene segments at different sites of the Shewanella genome with an efficiency approaching 100%. The inserted cargo genes could be kept stable on the genome after continuous cultivation. The enhancement of the organism's EET efficiency was realized through two primary strategies: the integration of the phenazine-1-carboxylic acid synthesis gene cluster to augment EET efficiency and the targeted disruption of the SO3350 gene to promote anodic biofilm development. Collectively, our findings highlight the potential of utilizing the INTEGRATE system for strategic genomic alterations, presenting a synergistic approach to augment the functionality of electroactive bacteria within bioelectrochemical systems.

Boosting Upconversion Efficiency in Optically Inert Shelled Structures with Electroactive Membrane through Electron Donation.

This study innovatively addresses challenges in enhancing upconversion efficiency in lanthanide-based nanoparticles (UCNPs) by exploiting Shewanella oneidensis MR-1, a microorganism capable of extracellular electron transfer. Electroactive membranes, rich in c-type cytochromes, are extracted from bacteria and integrated into membrane-integrated liposomes (MILs), encapsulating core-shelled UCNPs with an optically inactive shell, forming UCNP@MIL constructs. The electroactive membrane, tailored to donate electrons through the inert shell, independently boosts upconversion emission under near-infrared excitation (980 or 1550nm), bypassing ligand-sensitized UCNPs. The optically inactive shell restricts energy migration, emphasizing electroactive membrane electron donation. Density functional theory calculations elucidate efficient electron transfer due to the electroactive membrane hemes' highest occupied molecular orbital being higher than the valence band maximum of the optically inactive shell, crucial for enhancing energy transfer to emitter ions. The introduction of a SiO2 insulator coating diminishes light enhancement, underscoring the importance of unimpeded electron transfer. Luminescence enhancement remains resilient to variations in emitter or sensitizing ions, highlighting the robustness of the electron transfer-induced phenomenon. However, altering the inert shell material diminishes enhancement, emphasizing the role of electron transfer. This methodology holds significant promise for diverse biological applications. UCNP@MIL offers an advantage in cellular uptake, which proves beneficial for cell imaging.

Influence of support materials on the electroactive behavior, structure and gene expression of wild type and GSU1771-deficient mutant of Geobacter sulfurreducens biofilms.

Geobacter sulfurreducens DL1 is a metal-reducing dissimilatory bacterium frequently used to produce electricity in bioelectrochemical systems (BES). The biofilm formed on electrodes is one of the most important factors for efficient electron transfer; this is possible due to the production of type IV pili and c-type cytochromes that allow it to carry out extracellular electron transfer (EET) to final acceptors. In this study, we analyzed the biofilm formed on different support materials (glass, hematite (Fe2O3) on glass, fluorine-doped tin oxide (FTO) semiconductor glass, Fe2O3 on FTO, graphite, and stainless steel) by G. sulfurreducens DL1 (WT) and GSU1771-deficient strain mutant (Δgsu1771). GSU1771 is a transcriptional regulator that controls the expression of several genes involved in electron transfer. Different approaches and experimental tests were carried out with the biofilms grown on the different support materials including structure analysis by confocal laser scanning microscopy (CLSM), characterization of electrochemical activity, and quantification of relative gene expression by RT-qPCR. The gene expression of selected genes involved in EET was analyzed, observing an overexpression of pgcA, omcS, omcM, and omcF from Δgsu1771 biofilms compared to those from WT, also the overexpression of the epsH gene, which is involved in exopolysaccharide synthesis. Although we observed that for the Δgsu1771 mutant strain, the associated redox processes are similar to the WT strain, and more current is produced, we think that this could be associated with a higher relative expression of certain genes involved in EET and in the production of exopolysaccharides despite the chemical environment where the biofilm develops. This study supports that G. sulfurreducens is capable of adapting to the electrochemical environment where it grows.

Boosting power output in microbial fuel cell with sulfur-doped MXene/polypyrrole hydrogel anode for enhanced extracellular electron transfer process

Boosting power output in microbial fuel cell with sulfur-doped MXene/polypyrrole hydrogel anode for enhanced extracellular electron transfer process

Surface roughness influence on extracellular electron microbiologically influenced corrosion of C1018 carbon steel by Desulfovibrio ferrophilus IS5 biofilm

Carbon steel microbiologically influenced corrosion (MIC) by sulfate reducing bacteria (SRB) is known to occur via extracellular electron transfer (EET). A higher biofilm sessile cell count leads to more electrons being harvested for sulfate reduction by SRB in energy production. Metal surface roughness can impact the severity of MIC by SRB because of varied biofilm attachment. C1018 carbon steel coupons (1.2 cm2 top working surface) polished to 36 grit (4.06 μm roughness which is relatively rough) and 600 grit (0.13 μm) were incubated in enriched artificial seawater inoculated with highly corrosive Desulfovibrio ferrophilus IS5 at 28 ℃ for 7 d and 30 d. It was found that after 7 d of SRB incubation, 36 grit coupons had a 11% higher sessile cell count at (2.0 ± 0.17) × 108 cells/cm2, 52% higher weight loss at 22.4 ± 5.9 mg/cm2 (1.48 ± 0.39 mm/a uniform corrosion rate), and 18% higher maximum pit depth at 53 μm compared with 600 grit coupons. However, after 30 d, the differences diminished. Electrochemical tests with transient information supported the weight loss data trends. This work suggests that a rougher surface facilitates initial biofilm establishment but provides no long-term advantage for increased biofilm growth.

Variations in flavin redox states during extracellular electron transfer and electron conduction in Shewanella oneidensis

Flavin is one of the most prevalent redox molecules utilized by electroactive bacteria. Electroactive bacteria form a three-dimensional architecture with multiple cell assemblages on electrodes in bioelectrochemical systems. This provokes the importance of unveiling the redox chemistry of flavins during electron transfer not only at the bacteria/electrode interface but also inside cell assemblages. However, it has been difficult to directly compare the redox species contributing to each electron transfer reaction. In this study, to simultaneously detect the flavin redox species at the electrode surface and those in cell assemblages, we conducted bipotentiometric cyclic voltammetry on a colony of Shewanella oneidensis MR-1. The bipotentiometric data showed that flavin mononucleotide proceeds the redox cycle at − 0.43 V (vs. standard hydrogen electrode) in the MR-1 colony assignable to the semiquinone/hydroquinone redox cycle, which was supported by experiments with semiquinone scavenger and gene deletion mutants. Notably, the peak at − 0.43 V was not detected at the electrode surface, indicating that the flavin redox cycles and redox potentials involved in the electron transfer inside MR-1 assemblages differ from those at the MR-1/electrode interface. The measurement system presented herein offers a platform to clarify the redox reactions in cell assemblages as well as at the bacteria/electrode interface.

DNA‐rGO Aerogel Bioanodes with Microcompartmentalization for High‐Performance Bioelectrochemical Systems

AbstractBioelectrochemical systems (BES) have garnered significant attention for their applications in renewable energy, microbial fuel cells, biocatalysis, and bioelectronics. In BES, bioelectrodes are used to facilitate extracellular electron transfer among microbial biocatalysts. This study is focused on enhancing the efficiency of these processes through microcompartmentalization, a technique that strategically organizes and segregates microorganisms within the electrode, thereby bolstering BES output efficiency. The study introduces a deoxyribonucleic acid (DNA)‐based reduced graphene oxide (rGO) aerogel engineered as a bioanode to facilitate microorganism compartmentalization while providing an expanded biocompatible surface with continuous conductivity. The DNA‐rGO aerogel is synthesized through the self‐assembly of graphene oxide and DNA, with thermal reduction imparting lightweight structural stability and conductivity to the material. The DNA component serves as a hydrophilic framework, enabling precise regulation of compartment size and biofunctionalization of the rGO surface. To evaluate the performance of this aerogel bioanode, measurements of current generation are conducted using Shewanella oneidensis MR‐1 bacteria as a model biocatalyst. The bioanode exhibits a current density reaching up to 1.5 A·m⁻2, surpassing the capabilities of many existing bioanodes. With its abundant microcompartments, the DNA‐rGO demonstrates high current generation performance, representing a sustainable approach for energy harvesting without reliance on metals, polymers, or heterostructures.