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To target development of bioelectrochemical systems, we developed an advanced microfluidic method to identify reaction bottlenecks in the metabolic activity of a pure‐culture Geobacter sulfurreducens electroactive biofilm (EAB). The microfluidic system was devised to include perpendicular flow orientation for improved boundary layer uniformity and was combined with an embedded 3‐electrode system to accurately apply a constant potential during the entire experimental duration which lasted se. A 3‐sensor temperature control system provided the basis of accurate temperature pulsing, which modified the EAB metabolic activity over short time intervals relative to the bacterial doubling rate. The system, together with the unique ability to control hydrodynamic, electrochemical, and thermal conditions, was used as the basis for an Arrhenius approach to obtain activation energy barrier values at different growth times, acetate concentrations, and flow rates. The results indicated that bottlenecks in the overall metabolic activity after 1 month of growth time were related to electron transfer through extracellular cytochrome c. After the EAB further matured to 4 months old, the bottleneck appeared to switch to enzyme‐driven acetate oxidation. Based on this hypothesis, we observed after 4‐months, that strong increases in effective enzyme concentration were primarily obtained by increasing flow rate, and secondarily by increasing acetate concentration [ABSTRACT FROM AUTHOR]

Bioelectrochemical anaerobic ammonium oxidation (anammox) systems allow eco-friendly removal of nitrogen from reject wastewater coming from biogas processing as the anammox bacteria have previously shown to have c-type cytochromes acting in the extracellular electron transport (EET) mechanism between the bacteria and electrode. The anammoxosome compartment present in anammox bacteria features a highly curved membrane and contains tubular structures along with electron-dense particles that contain iron, which could enhance the process of EET and enhance nitrogen removal by properly applied potentials. In this study, nitrogen removal was investigated in the electrostimulated anammox nitrogen removal (EANR) cells operated comparatively at open circuit and at applied potentials of − 300 mV, − 500 mV, and − 700 mV vs. Ag/AgCl. At peak performance (at − 700 mV vs. Ag/AgCl), the EANR showed up to 140% higher specific nitrogen removal rate (11.2 ± 0.3 g N/m2/day) compared to the control reactors without applied potential (8.3 ± 0.2 g N/m2/day). The microbial community on the cathode with the applied potential had a higher relative proportion of unclassified Candidatus Brocadia (7.5%) compared to inoculum (> 0.01%), in contrast to cathode without potential (0.74%) and control (0.2%). The EANR system demonstrated to achieve ammonium and nitrite removal efficiencies of 91% and 53%, respectively, during a 24-h test cycle from an initial TN concentration of ~ 100 mg N/L. After 150 h, it achieved complete removal of all nitrogen compounds, reaching a 100% removal efficiency. The EANR would be very useful in the establishment of field-scale bilateral anammox-bioelectrochemical technology combining microbial fuel cell bioanodes and EANR biocathodes for wastewater treatment. [ABSTRACT FROM AUTHOR]

gLiving materials can achieve unprecedented function by combining synthetic materials with the wide range of cellular functions. Of interest are situations where the critical properties of individual abiotic and biotic elements improve via their combination. For example, integrating electroactive bacteria into conjugated polyelectrolyte (CPE) hydrogels increases biocurrent production. One observes more efficient electrical charge transport within the CPE matrix in the presence of Shewanella oneidensis MR‐1 and more current per cell is extracted, compared to traditional biofilms. Here, the origin of these synergistic effects are examined. Transcriptomics reveals that genes in S. oneidensis MR‐1 related to bacteriophages and energy metabolism are upregulated in the composite material. Fluorescent staining and rheological measurements before and after enzymatic treatment identified the importance of extracellular biomaterials in increasing matrix cohesion. The synergy between CPE and S. oneidensis MR‐1 thus arises from initially unanticipated changes in matrix composition and bacteria adaption within the synthetic environment. [ABSTRACT FROM AUTHOR]

Microbial electrochemical technologies represent innovative approaches to contaminated soil and groundwater remediation and provide a flexible framework for removing organic and inorganic contaminants by integrating electrochemical and biological techniques. To simulate in situ microbial electrochemical treatment of groundwater plumes, this study investigates Cr(VI) reduction within a bioelectrochemical continuous flow (BECF) system equipped with soil‐buried electrodes, comparing it to abiotic and open‐circuit controls. Continuous‐flow systems were tested with two chromium‐contaminated solutions (20–50 mg Cr(VI)/L). Additional nutrients, buffers, or organic substrates were introduced during the tests in the systems. With an initial Cr(VI) concentration of 20 mg/L, 1.00 mg Cr(VI)/(L day) bioelectrochemical removal rate in the BECF system was observed, corresponding to 99.5% removal within nine days. At the end of the test with 50 mg Cr(VI)/L (156 days), the residual Cr(VI) dissolved concentration was two orders of magnitude lower than that in the open circuit control, achieving 99.9% bioelectrochemical removal in the BECF. Bacteria belonging to the orders Solirubrobacteriales, Gaiellales, Bacillales, Gemmatimonadales, and Propionibacteriales characterized the bacterial communities identified in soil samples; differently, Burkholderiales, Mycobacteriales, Cytophagales, Rhizobiales, and Caulobacterales characterized the planktonic bacterial communities. The complexity of the microbial community structure suggests the involvement of different microorganisms and strategies in the bioelectrochemical removal of chromium. In the absence of organic carbon, microbial electrochemical removal of hexavalent chromium was found to be the most efficient way to remove Cr(VI), and it may represent an innovative and sustainable approach for soil and groundwater remediation. Integr Environ Assess Manag 2024;20:2033–2049. © 2024 The Author(s). Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC). Key Points: The research offers valuable insights that can contribute to advancing microbial electrochemical remediation systems designed to reduce Cr(VI) in water‐saturated soils.There were substantial differences from previously reported studies: acclimatization and/or adaptation and transfer of the electroactive bacterial community to Cr(VI) to a bioelectrochemical continuous flow system, no ion exchange membranes, and no nutrients and/or organic carbon added.The research was conducted to simulate most realistically the real conditions of Cr(VI)‐contaminated aquifers, in terms of solid‐to‐liquid ratio, interactions among soil phases, and physicochemical parameters (pH and electrical conductivity).The outcomes achieved in the system for Cr(VI) reduction in water‐saturated soil can demonstrate the feasibility of employing microbial electrochemical technology for the in situ treatment of contaminated aquifers, with interesting implications for economic and environmental sustainability. [ABSTRACT FROM AUTHOR]

The successful application of bioelectrochemical systems in the future depends on the improving of electrode performance while decreasing material costs. This study explores the use of chitosan supported on different kinds of carbon materials to modify graphite electrode for the electricity generation performance of Geobacter sulfurreducens. The novel hierarchically carbon composites modified electrodes were obtained by a simple and environment‐friendly method. Among the proposed composites, the optimal composite CS/CB (5 h) possessed a better performance for the promotion of electrochemically active biofilm (EAB) growth and enhancing current generation compared with other composites. Based on morphological, chemical, and electrochemical evidences, we conclude that the CB was coated on the surface of CS to form the CS/CB decorated graphite electrode, and CS/CB (5 h) electrode exhibited significant load‐bearing capacity for bacteria colonization and enhanced the contact between bacteria and electrode, which improved the direct electron transfer process. The microbial three‐electrode system equipped CS/CB (5 h) device delivered a high current density of 1457±69 μA/cm2. The current density was increased to 3 times higher than that of the unmodified electrode. The use of this CS/CB (5 h) composite can substantially improves EAB growth and enhance power production of bioelectrochemical systems. [ABSTRACT FROM AUTHOR]

Microbial fuel cells (MFCs) represent a promising technology for sustainable energy generation, which leverages the metabolic activities of microorganisms to convert organic substrates into electrical energy. In oil spill scenarios, hydrocarbonoclastic biofilms naturally form at the water–oil interface, creating a distinct environment for microbial activity. In this work, we engineered a novel MFC that harnesses these biofilms by strategically positioning the positive electrode at this critical junction, integrating the biofilm's natural properties into the MFC design. These biofilms, composed of specialized hydrocarbon-degrading bacteria, are vital in supporting electron transfer, significantly enhancing the system's power generation. Next-generation sequencing and scanning electron microscopy were used to characterize the microbial community, revealing a significant enrichment of hydrocarbonoclastic Gammaproteobacteria within the biofilm. Notably, key genera such as Paenalcaligenes, Providencia, and Pseudomonas were identified as dominant members, each contributing to the degradation of complex hydrocarbons and supporting the electrogenic activity of the MFCs. An electrochemical analysis demonstrated that the MFC achieved a stable power output of 51.5 μW under static conditions, with an internal resistance of about 1.05 kΩ. The system showed remarkable long-term stability, which maintained consistent performance over a 5-day testing period, with an average daily energy storage of approximately 216 mJ. Additionally, the MFC effectively recovered after deep discharge cycles, sustaining power output for up to 7.5 h before requiring a recovery period. Overall, the study indicates that MFCs based on hydrocarbonoclastic biofilms provide a dual-functionality system, combining renewable energy generation with environmental remediation, particularly in wastewater treatment. Despite lower power output compared to other hydrocarbon-degrading MFCs, the results highlight the potential of this technology for autonomous sensor networks and other low-power applications, which required sustainable energy sources. Moreover, the hydrocarbonoclastic biofilm-based MFC presented here offer significant potential as a biosensor for real-time monitoring of hydrocarbons and other contaminants in water. The biofilm's electrogenic properties enable the detection of organic compound degradation, positioning this system as ideal for environmental biosensing applications. [ABSTRACT FROM AUTHOR]

Hydroponic cultivation is an efficient, resource-saving technology that produces high yields of high-quality products per unit area without soil. While this technology can save water and fertilisers, water recirculation increases the accumulation of root exudates known to be toxic to the plant, causing growth inhibition. The usage of bioelectrochemical systems (BESs) is well-documented for wastewater treatment, desalination, contamination remediation, bioelectricity generation, etc. In this review we explore the issues associated with the usage of traditional approaches in detecting and removing the phytotoxic substances exudated from plant roots. Furthermore, we investigate the prospects of deploying BESs in hydroponic systems and highlight potential benefits and challenges. The application, feasibility and scalability of BES-hydroponic systems, as well as the possibility of integration with other technologies are all critically discussed. It is concluded that the use of BESs for hydroponic wastewater treatment and for real-time plant growth monitoring represents a novel and valuable strategy. This approach has the potential to overcome limitations of the existing treatment methods and contribute to the advancement of sustainable agriculture. [ABSTRACT FROM AUTHOR]

Despite over two decades of intense research into bioelectrochemical systems (BESs), their practical implementation remains unrealized, partly due to the low performance of bioelectrodes. With the introduction of additive manufacturing techniques, the development of a new generation of bioelectrodes with custom-shaped geometries using conductive composites has become feasible. This study examines the potential of using two conductive composites, Poly-lactic acid (PLA) and thermoplastic polyurethane (TPU), for 3D-printed electrodes. Electrochemical characterization reveals that TPU has a charge transfer resistance approximately two orders of magnitude higher than PLA, rendering it unsuitable for bioelectrodes. The presence of triangular patterns enhances the performance of planar electrodes, with optimal results observed for PLA-based electrodes with surface pattern depths between 0.6 and 1.4 mm. Additionally, electrodeposition (ED) of graphene oxide (GO) further improves performance across all cases. During the subsequent biotic start-up, patterned PLA electrodes with a depth of 1.4 mm exhibit higher current. However, these 3D-printed electrodes exhibit degradation after 56 days of operation. [ABSTRACT FROM AUTHOR]

High power output and high conversion efficiency are crucial parameters for microbial fuel cells (MFCs). In our previous work, we worked with microfluidic MFCs to study fundamentals related to the power density of the MFCs, but nutrient consumption was limited to one side of the microchannel (the electrode layer) due to diffusion limitations. In this work, long-term experiments were conducted on a new four-electrode microfluidic MFC design, which grew Geobacter sulfurreducens biofilms on upward- and downward-facing electrodes in the microchannel. To our knowledge, this is the first study comparing electroactive biofilm (EAB) growth experiencing the influence of opposing gravitational fields. It was discovered that inoculation and growth of the EAB did not proceed as fast at the downward-facing anode, which we hypothesize to be due to gravity effects that negatively impacted bacterial settling on that surface. Rotating the device during the growth phase resulted in uniform and strong outputs from both sides, yielding individual power densities of 4.03 and 4.13 W m−2, which increased to nearly double when the top- and bottom-side electrodes were operated in parallel as a single four-electrode MFC. Similarly, acetate consumption could be doubled with the four electrodes operated in parallel. [ABSTRACT FROM AUTHOR]

Bioelectrochemical systems (BES) have emerged as a sustainable and highly promising technology that has garnered significant attention from researchers worldwide. These systems provide an efficient platform for the removal and recovery of valuable products from wastewater, with minimal or no net energy loss. Among the various types of BES, microbial fuel cells (MFCs) are a notable example, utilizing microbial biocatalytic activities to generate electrical energy through the degradation of organic matter. Other BES variants include microbial desalination cells (MDCs), microbial electrolysis cells (MECs), microbial electrosynthesis cells (MXCs), microbial solar cells (MSCs), and more. BESs have demonstrated remarkable potential in the recovery of diverse products such as hydrogen, methane, volatile fatty acids, precious nutrients, and metals. Recent advancements in scaling up BESs have facilitated a more realistic assessment of their net energy recovery and resource yield in real-world applications. This comprehensive review focuses on the practical applications of BESs, from laboratory-scale developments to their potential for industrial commercialization. Specifically, it highlights successful examples of value-added product recovery achieved through various BES configurations. Additionally, this review critically evaluates the limitations of BESs and provides suggestions to enhance their performance at a larger scale, enabling effective implementation in real-world scenarios. By providing a thorough analysis of the current state of BES technology, this review aims to emphasize the tremendous potential of these systems for sustainable wastewater treatment and resource recovery. It underscores the significance of bridging the gap between laboratory-scale achievements and industrial implementation, paving the way for a more sustainable and resource-efficient future. [ABSTRACT FROM AUTHOR]

Pseudomonas putida , a Gram-negative aerobe widely used in biotechnological applications, has attracted attention as a novel exoelectrogen in BESs. BESs exploit the EET capability of exoelectrogens in microbial fuel cells, microbial electrolysis cells, microbial electrosynthesis, and microbial desalination cells. EET enables anaerobic respiration with various external redox-active surfaces such as electrodes and metal oxides, allowing energy conversion and electron transfer both inside and outside the cell. The performance of BESs with P. putida as the exoelectrogen is affected by key factors such as substrates, electrode materials, and EET pathways. BESs with P. putida as the exoelectrogen have been used for removal of organics, the biosynthesis of valuable chemicals, and environmental toxicity testing. Bioelectrochemical systems (BESs), a group of promising integrated systems that combine the advantages of biotechnology and electrochemical techniques, offer new opportunities to address environmental and energy challenges. Exoelectrogens capable of extracellular electron transfer (EET) are the critical factor enabling electrocatalytic activity in BESs. Pseudomonas putida , an aerobe widely used in environmental bioremediation, the biosynthesis of valuable chemicals, and energy bioproduction, has attracted much attention due to its unique application potential in BESs. This review provides a comprehensive understanding of the working principles, key factors, and applications of BESs using P. putida as the exoelectrogen. The challenges and perspectives for the development of BESs with P. putida as the exoelectrogen are also proposed and discussed. [ABSTRACT FROM AUTHOR]

Chlorinated organic compounds (COCs) are typical refractory organic compounds, having high biological toxicity. These compounds are a type of pervasive pollutants that can be present in polluted soil, air, and various types of waterways, such as groundwater, rivers, and lakes, posing a significant threat to the ecological environment and human health. Bioelectrochemical systems (BESs) are an effective strategy for the degradation of bio-refractory compounds. BESs improve the waste treatment efficiency through the application of weak electrical stimulation. This review discusses the processes of BESs configurations and degradation performances in different environmental media including wastewater, soil, waste gas and groundwater. In addition, the degradation mechanisms and performance-enhancing additives are summarized. The future challenges and perspectives on the development of BES for COCs removal are briefly discussed. [ABSTRACT FROM AUTHOR]

Abstract Bioelectrochemical systems (BES) is a new and expanding technology that can simultaneously convert chemical energy into electrical energy by removing nutrients. The present study investigated the BES in removing nitrogen compounds and produce electricity. To this end, a BES reactor with two chambers of cathode and anode and nafion 117 membrane was used as a separator between the two chambers. Then, the BES performance at different concentrations of COD and primary ammonium at different retention times was investigated to remove nitrogen compounds and organic matter. Voltage, current and power density were measured. The results showed that the maximum COD removal efficiency was 73.2 % for the substrate concentration of 2000 mg/L, which decreased to 72.6 % when the substrate concentration increased to 10000 mg/L. The maximum removal efficiency of nitrogen compounds was 83.4 % at COD 10000 mg/L and the initial ammonium concentration was 50 mg/L. The maximum voltage, current and power density in this phase were 391 mV, 460 mA/m2, 63/48 mW/m2, respectively. The results of the study showed that BES can be used as a suitable method to remove high amounts of ammonium in wastewater and organic materials and simultaneously produce electricity.

Abstract gLiving materials can achieve unprecedented function by combining synthetic materials with the wide range of cellular functions. Of interest are situations where the critical properties of individual abiotic and biotic elements improve via their combination. For example, integrating electroactive bacteria into conjugated polyelectrolyte (CPE) hydrogels increases biocurrent production. One observes more efficient electrical charge transport within the CPE matrix in the presence of Shewanella oneidensis MR‐1 and more current per cell is extracted, compared to traditional biofilms. Here, the origin of these synergistic effects are examined. Transcriptomics reveals that genes in S. oneidensis MR‐1 related to bacteriophages and energy metabolism are upregulated in the composite material. Fluorescent staining and rheological measurements before and after enzymatic treatment identified the importance of extracellular biomaterials in increasing matrix cohesion. The synergy between CPE and S. oneidensis MR‐1 thus arises from initially unanticipated changes in matrix composition and bacteria adaption within the synthetic environment.

Abstract Bioelectrochemical 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.

In the present study, the potential of Pseudomonas citronellolis 620C strain was evaluated, for the first time, to generate electricity in a standard, double chamber microbial fuel cell (MFC), with oily wastewater (OW) being the fuel at 43.625 mg/L initial chemical oxygen demand (COD). Both electrochemical and physicochemical results suggested that this P. citronellolis strain utilized efficiently the OW substrate and generated electricity in the MFC setup reaching 0.05 mW/m2 maximum power. COD removal was remarkable reaching 83.6 ± 0.1%, while qualitative and quantitative gas chromatography/mass spectrometry (GC/MS) analysis of the OW total petroleum and polycyclic aromatic hydrocarbons, and fatty acids revealed high degradation capacity. It was also determined that P. citronellolis 620C produced pyocyanin as electron shuttle in the anodic MFC chamber. To the authors' best knowledge, this is the first study showing (phenazine-based) pyocyanin production from a species other than P. aeruginosa and, also, the first time that P. citronellolis 620C has been shown to produce electricity in a MFC. The production of pyocyanin, in combination with the formation of biofilm in the MFC anode, as observed with scanning electron microscopy (SEM) analysis, makes this P. citronellolis strain an attractive and promising candidate for wider MFC applications. [ABSTRACT FROM AUTHOR]

Microbial biofilms present one of the most widespread forms of life on Earth. The formation of microbial communities on various surfaces presents a major challenge in a variety of fields, including medicine, the food industry, shipping, etc. At the same time, this process can also be used for the benefit of humans—in bioremediation, wastewater treatment, and various biotechnological processes. The main direction of using electroactive microbial biofilms is their incorporation into the composition of biosensor and biofuel cells This review examines the fundamental knowledge acquired about the structure and formation of biofilms, the properties they have when used in bioelectrochemical devices, and the characteristics of the formation of these structures on different surfaces. Special attention is given to the potential of applying the latest advances in genetic engineering in order to improve the performance of microbial biofilm-based devices and to regulate the processes that take place within them. Finally, we highlight possible ways of dealing with the drawbacks of using biofilms in the creation of highly efficient biosensors and biofuel cells. [ABSTRACT FROM AUTHOR]

Environmental pollution and energy scarcity are the two significant issues that could substantially impede the sustainable growth of our civilization. Microbial fuel cells (MFCs) are an emerging technique for converting the chemical energy of organic wastes directly into electric energy, allowing for both energy recovery and environmental rehabilitation. Solid organic waste decomposition is generally more challenging compared to organic wastewater due to several factors, including the nature of the waste, the decomposition process, and the associated environmental and logistical considerations. With rapid population expansion and acceleration of urbanization, waste generation continues to rise globally, causing complicated environmental, socioeconomic, and energy problems and a growing demand for public health globally. Bioelectrochemical systems (BES) are promising solid waste management options. However, BES may not be the most effective solution on its own for certain types of waste or may be incapable of treating all waste components. In many circumstances, combining BES with other solid treatment technologies can increase overall treatment efficiency and waste management. Combining BES with other solid treatment methods can have synergistic effects, boosting waste treatment efficiency, resource recovery, and environmental sustainability. However, to guarantee the successful integration and optimization of these combined approaches, site-specific factors, waste characteristics, and system compatibility must be considered. [ABSTRACT FROM AUTHOR]

A microbial fuel cell (MFC) consisting of a bacterial anode chamber and a microalgal cathode chamber was operated under various conditions to assess its technical feasibility. Maximum achievable power density reached up to 7.13 mW m–2. The traditional MFC process of conversion of carbon sources to bioelectricity in the anodic chamber was compared with a system circulating anodic effluent to the cathode chamber. The bacteria and microalgae simultaneously carried out the carbon recycling and recovery of energy and resources synergizing the performance of MFC. Results indicated a comparable chemical oxygen demand removal efficiencies at 50% of the retention time compared to the traditional system. The dissolved oxygen concentration varied between 11.95 and 7.44 mg L–1 with Chlorella vulgaris under alternative light and dark cycles. Despite the variations in electricity output, the system showed its technical feasibility to harness energy for photosynthesis under natural sunlight conditions. [ABSTRACT FROM AUTHOR]

Sulphur plays a fundamental role in the biological processes of chemolithotrophic microorganisms. Due to the redox characteristics of sulphur, microorganisms use it for metabolic processes. Such is the case of the dissimilatory processes in the anaerobic respiration of reducing microorganisms. The production of electrical energy from the metabolism of native microorganisms using sulphur as substrate from inorganic mineral sources in the form of Galena (PbS) was achieved using MR mineral medium with 15% (w/v) of PbS mineral concentrate. At 400 h of growth, the highest voltage produced in an experimental unit under anaerobic conditions was 644 mV. The inoculum was composed of microorganisms with spiral morphology, and at the final stages of energy production, the only microorganism identified was Bacillus clausii. This microorganism has not been reported in bioelectrochemical systems, but it has been reported to be present in corrosive environments and reducing anoxic environments.

Microbial fuel cells (MFCs) represent a promising technology for sustainable energy generation, which leverages the metabolic activities of microorganisms to convert organic substrates into electrical energy. In oil spill scenarios, hydrocarbonoclastic biofilms naturally form at the water–oil interface, creating a distinct environment for microbial activity. In this work, we engineered a novel MFC that harnesses these biofilms by strategically positioning the positive electrode at this critical junction, integrating the biofilm’s natural properties into the MFC design. These biofilms, composed of specialized hydrocarbon-degrading bacteria, are vital in supporting electron transfer, significantly enhancing the system’s power generation. Next-generation sequencing and scanning electron microscopy were used to characterize the microbial community, revealing a significant enrichment of hydrocarbonoclastic Gammaproteobacteria within the biofilm. Notably, key genera such as Paenalcaligenes, Providencia, and Pseudomonas were identified as dominant members, each contributing to the degradation of complex hydrocarbons and supporting the electrogenic activity of the MFCs. An electrochemical analysis demonstrated that the MFC achieved a stable power output of 51.5 μW under static conditions, with an internal resistance of about 1.05 kΩ. The system showed remarkable long-term stability, which maintained consistent performance over a 5-day testing period, with an average daily energy storage of approximately 216 mJ. Additionally, the MFC effectively recovered after deep discharge cycles, sustaining power output for up to 7.5 h before requiring a recovery period. Overall, the study indicates that MFCs based on hydrocarbonoclastic biofilms provide a dual-functionality system, combining renewable energy generation with environmental remediation, particularly in wastewater treatment. Despite lower power output compared to other hydrocarbon-degrading MFCs, the results highlight the potential of this technology for autonomous sensor networks and other low-power applications, which required sustainable energy sources. Moreover, the hydrocarbonoclastic biofilm-based MFC presented here offer significant potential as a biosensor for real-time monitoring of hydrocarbons and other contaminants in water. The biofilm’s electrogenic properties enable the detection of organic compound degradation, positioning this system as ideal for environmental biosensing applications.

Sulphur plays a fundamental role in the biological processes of chemolithotrophic microorganisms. Due to the redox characteristics of sulphur, microorganisms use it for metabolic processes. Such is the case of the dissimilatory processes in the anaerobic respiration of reducing microorganisms. The production of electrical energy from the metabolism of native microorganisms using sulphur as substrate from inorganic mineral sources in the form of Galena (PbS) was achieved using MR mineral medium with 15% (w/v) of PbS mineral concentrate. At 400 h of growth, the highest voltage produced in an experimental unit under anaerobic conditions was 644 mV. The inoculum was composed of microorganisms with spiral morphology, and at the final stages of energy production, the only microorganism identified was Bacillus clausii. This microorganism has not been reported in bioelectrochemical systems, but it has been reported to be present in corrosive environments and reducing anoxic environments. [ABSTRACT FROM AUTHOR]

In the context of the anaerobic ammonium oxidation process (anammox), great scientific advances have been made over the past two decades, making anammox a consolidated technology widely used worldwide for nitrogen removal from wastewaters. This review provides a detailed and comprehensive description of the anammox process, the microorganisms involved and their metabolism. In addition, recent research on the application of the anammox process with alternative electron acceptors is described, highlighting the biochemical reactions involved, its advantages and potential applications for specific wastewaters. An updated description is also given of studies reporting the ability of microorganisms to couple the anammox process to extracellular electron transfer to insoluble electron acceptors; particularly iron, carbon-based materials and electrodes in bioelectrochemical systems (BES). The latter, also referred to as anodic anammox, is a promising strategy to combine the ammonium removal from wastewater with bioelectricity production, which is discussed here in terms of its efficiency, economic feasibility, and energetic aspects. Therefore, the information provided in this review is relevant for future applications. [ABSTRACT FROM AUTHOR]

Currently, the industrial application of bioelectrochemical systems (BESs) that are incubated with natural electrochemically active microbes (EABs) is limited due to inefficient extracellular electron transfer (EET) by natural EABs. Notably, recent studies have identified several novel living biomaterials comprising highly efficient electron transfer systems allowing unparalleled proficiency of energy conversion. Introduction of these biomaterials into BESs could fundamentally increase their utilization for a wide range of applications. This review provides a comprehensive assessment of recent advancements in the design of living biomaterials that can be exploited to enhance bioelectrocatalytic performance. Further, modular configurations of abiotic and biotic components promise a powerful enhancement through integration of nano-based artificial mediators and synthetic biology. Herein, recent advancements in BESs are synthesized and assessed, including heterojunctions between conductive nanomaterials and EABs, in-situ hybrid self-assembly of EABs and nano-sized semiconductors, cytoprotection in biohybrids, synthetic biological modifications of EABs and electroactive biofilms. Since living biomaterials comprise a broad range of disciplines, such as molecular biology, electrochemistry and material sciences, full integration of technological advances applied in an interdisciplinary framework will greatly enhance/advance the utility and novelty of BESs. Overall, emerging fundamental knowledge concerning living biomaterials provides a powerful opportunity to markedly boost EET efficiency and facilitate the industrial application of BESs to meet global sustainability challenges/goals.

Despite over two decades of intense research into bioelectrochemical systems (BESs), their practical implementation remains unrealized, partly due to the low performance of bioelectrodes. With the introduction of additive manufacturing techniques, the development of a new generation of bioelectrodes with custom-shaped geometries using conductive composites has become feasible. This study examines the potential of using two conductive composites, Poly-lactic acid (PLA) and thermoplastic polyurethane (TPU), for 3D-printed electrodes. Electrochemical characterization reveals that TPU has a charge transfer resistance approximately two orders of magnitude higher than PLA, rendering it unsuitable for bioelectrodes. The presence of triangular patterns enhances the performance of planar electrodes, with optimal results observed for PLA-based electrodes with surface pattern depths between 0.6 and 1.4 mm. Additionally, electrodeposition (ED) of graphene oxide (GO) further improves performance across all cases. During the subsequent biotic start-up, patterned PLA electrodes with a depth of 1.4 mm exhibit higher current. However, these 3D-printed electrodes exhibit degradation after 56 days of operation.

High power output and high conversion efficiency are crucial parameters for microbial fuel cells (MFCs). In our previous work, we worked with microfluidic MFCs to study fundamentals related to the power density of the MFCs, but nutrient consumption was limited to one side of the microchannel (the electrode layer) due to diffusion limitations. In this work, long-term experiments were conducted on a new four-electrode microfluidic MFC design, which grew Geobacter sulfurreducens biofilms on upward- and downward-facing electrodes in the microchannel. To our knowledge, this is the first study comparing electroactive biofilm (EAB) growth experiencing the influence of opposing gravitational fields. It was discovered that inoculation and growth of the EAB did not proceed as fast at the downward-facing anode, which we hypothesize to be due to gravity effects that negatively impacted bacterial settling on that surface. Rotating the device during the growth phase resulted in uniform and strong outputs from both sides, yielding individual power densities of 4.03 and 4.13 W m−2, which increased to nearly double when the top- and bottom-side electrodes were operated in parallel as a single four-electrode MFC. Similarly, acetate consumption could be doubled with the four electrodes operated in parallel.

Effects of electron shuttle (ES) concentration on biofilm formation and redox activity and the molecular mechanism of inducing biofilm formation remain underexplored. Here, we examine the impacts of 2,6-di-tert-butyl-p-benzoquinone (2,6-DTBBQ) on the initial formation and redox activity of biofilms in bioelectrochemical systems (BESs) with Klebsiella quasipneumoniae SP203. The BES with 5-mM 2,6-DTBBQ has higher voltage output (increased approx. 103.53%) than control group, owing to the stimulation of redox reaction and reduction of the internal resistance of BESs. The 10-mM 2,6-DTBBQ enhances biofilm formation but inhibited redox activity of biofilm. Five-millimolar 2,6-DTBBQ promotes the extracellular electron transfer (EET) process with accumulated polysaccharides and high-density protein. CLSM results demonstrates high-density protein catalyze redox activity of biofilm by live/dead cell ratio though no thick biofilm obtained. Moreover, the redox activity and C4-HSL of K. quasipneumoniae SP203 can be stimulated by 2,6-DTBBQ; this strain can respond to 2,6-DTBBQ levels to improve Fe-S clusters/NADH dehydrogenase assembly and the synthesis of NAD and ubiquinone. Based on these results, an EET mechanism of K. quasipneumoniae SP203 is proposed. Collectively, 2,6-DTBBQ can strengthen K. quasipneumoniae SP203 biofilm redox activity and EET, which may contribute to the provision of green energy in the field of low-power supply. [ABSTRACT FROM AUTHOR]

Microbial desalination cells (MDCs) exhibited an economical value with large promises as a useful desalination treatment solution. MDCs threefold applications to efficiently treat wastewater and to produce electricity and simultaneously accomplish desalination were investigated in this work. The study examined the influence of various performance parameters including co-substrate, temperature, pH, and salt concentrations on the response of three-chamber MDCs with respect to energy recovery and contaminant removal (Phenol). The system evaluation criteria encompassed chemical oxygen demand (COD), phenol removal efficiency, Coulombic efficiency, desalination efficiency, and other system parameters such as voltage generation and power density. The maximum COD and phenol removal efficiencies obtained at temperature = 37 °C, pH = 7, and salt concentration = 10,000 ppm, were 80% and 74%, respectively. The maximum Coulombic efficiency was 5.3% and was observed at temperature = 18 °C, pH = 7, and salt concentration = 10,000 ppm. The results show that the presence of a co-substrate improved power density; the maximum power density obtained was 52.9 mW/m2. The principal component analysis elucidated the impact of pH on COD and phenol removal rates. With our findings confirmed trends in the improvement of the voltage generation, COD and phenol removal efficiencies with the addition of a co-substrate, the temperature and pH increase. [ABSTRACT FROM AUTHOR]

Microbial biofilms present one of the most widespread forms of life on Earth. The formation of microbial communities on various surfaces presents a major challenge in a variety of fields, including medicine, the food industry, shipping, etc. At the same time, this process can also be used for the benefit of humans—in bioremediation, wastewater treatment, and various biotechnological processes. The main direction of using electroactive microbial biofilms is their incorporation into the composition of biosensor and biofuel cells This review examines the fundamental knowledge acquired about the structure and formation of biofilms, the properties they have when used in bioelectrochemical devices, and the characteristics of the formation of these structures on different surfaces. Special attention is given to the potential of applying the latest advances in genetic engineering in order to improve the performance of microbial biofilm-based devices and to regulate the processes that take place within them. Finally, we highlight possible ways of dealing with the drawbacks of using biofilms in the creation of highly efficient biosensors and biofuel cells.

Bioelectrochemical systems (BESs) are emerging techniques that use biological production of current for versatile activities, including energy recovery and bioremediation. The development of high-performance three-dimensional (3D) electrodes has attracted attention for facilitating current production in BESs. Carbon-based electrodes have been commonly used in BESs, but metal electrodes are not generally employed because of their low biocompatibility with microbes. In this study, 3D stainless-steel electrodes, composed of octahedral lattice, were fabricated using the 3D printing technique. Heat treatment was conducted to form an iron-oxide layer on the electrode surface for increasing biocompatibility. Another crucial parameter that determines current production is the pitch length of a lattice electrode as it affects the surface area and substrate diffusion. The pitch length was optimized by testing the lattice electrodes with pitches ranging from 1.5 mm to 6.0 mm. The highest current, obtained with the 3.0 mm-pitch electrode, was 50% higher than that obtained with common 3D carbon-felt electrodes. These results demonstrate the usefulness of 3D lattice-structured metal electrodes in BESs. [ABSTRACT FROM AUTHOR]

The ability of some bacteria to perform Extracellular Electron Transfer (EET) has been explored in bioelectrochemical systems (BES) to obtain energy or chemicals from pure substances or residual substrates. Here, a new pyoverdine-producing Pseudomonas aeruginosa strain was isolated from an MFC biofilm oxidizing glycerol, a by-product of biodiesel production. Strain EL14 was investigated to assess its electrogenic ability and products. In an open circuit system (fermentation system), EL14 was able to consume glycerol and produce 1,3-propanediol, an unusual product from glycerol oxidation in P. aeruginosa. The microbial fuel cell (MFC) EL14 reached a current density of 82.4 mA m−2 during the first feeding cycle, then dropped sharply as the biofilm fell off. Cyclic voltammetry suggests that electron transfer to the anode occurs indirectly, i.e., through a redox substance, with redox peak at 0.22 V (vs Ag/AgCl), and directly probably by membrane redox proteins, with redox peak at 0.05 V (vs Ag/AgCl). EL14 produced added-value bioproducts, acetic and butyric acids, as well as 1,3 propanediol, in both fermentative and anodic conditions. However, the yield of 1,3-PDO from glycerol was enhanced from 0.57 to 0.89 (mol of 1,3-PDO mol−1 of glycerol) under MFC conditions compared to fermentation. This result was unexpected, since successful 1,3-PDO production is not usually associated with P. aeruginosa glycerol metabolism. By comparing EL14 genomic sequences related to the 1,3-PDO biosynthesis with P. aeruginosa reference strains, we observed that strain EL14 has three copies of the dhaT gene (1,3-propanediol dehydrogenase a different arrangement compared to other Pseudomonas isolates). Thus, this work functionally characterizes a bacterium never before associated with 1,3-PDO biosynthesis, indicating its potential for converting a by-product of the biodiesel industry into an emerging chemical product. [ABSTRACT FROM AUTHOR]

A bioelectrochemical system (BES) combining oxygenic and anoxygenic photosynthesis was investigated. The possibility of improving the composition of biogas by removing H2S and carbon dioxide in the anode zone of the bioelectrochemical system and obtaining additional energy has been established. The dynamics of HS-removal from model solutions in the BES anolyte at 3 operating modes were observed. Complete removal of sulfides in the anodic zone and the anaerobic photobioreactor was found in the BES operating option as a microbial fuel cell. At the same time, an increase in the concentration of sulfates was observed to varying degrees for the studied variants. The most probable mechanisms for the removal of H2S in this combined system are the oxidation of sulfides by sulfur photoautotrophic bacteria present in the mixed consortium to sulfates and the bioelectrochemical oxidation of hydrogen sulfide on the surface of the anode to elemental sulfur and its other forms. The obtained results with real biogas passed through the BES anolyte and the anaerobic photobioreactor (APBR) are also positive. A complete purification of the biogas from H2S and a significant removal of CO2 (81 % - 85 %) were achieved, where the CH4 content in the biogas reached 94.1 % - 96.2 %. [ABSTRACT FROM AUTHOR]

Bioelectrochemical systems (BESs) are an emerging technology for wastewater treatment and resource recovery. These systems facilitate electron transfer between microorganisms and electrodes, enabling their application in various fields, such as electricity production, bioremediation, biosensors, and biocatalysis. However, electrode biofilms, which play a critical role in BESs, face several challenges (e.g., a long acclimation period, low attached biomass, high electron transfer resistance, and poor tolerance and stability) that limit the development of this technology. Quorum sensing (QS) is a communication method among microorganisms that can enhance the performance of BESs by regulating electrode biofilms. QS regulation can positively impact electrode biofilms by enhancing extracellular electron transfer (EET), biofilm formation, cellular activity, the secretion of extracellular polymeric substances (EPS), and the construction of microbial community. In this paper, the characteristics of anode electrogenic biofilms and cathode electrotrophic biofilms in BESs, EET mechanisms, and the main factors affecting biofilm formation were summarized. Additionally, QS regulation mechanisms for biofilm formation, strategies for enhancing and inhibiting QS, and the application of QS regulation for electrode biofilms in BESs were systematically reviewed and discussed. This paper provides valuable background information and insights for future research and development of BES platforms based on QS regulation of electrode biofilms. [ABSTRACT FROM AUTHOR]

Bioelectrochemical systems hold the promise of enabling sustainable microbial‐mediated energy interconversion between electrical and chemical energy. Herein, it is demonstrated how a single conjugated polymer can be used to enhance bidirectional extracellular electron transfer through forming self‐assembled coatings on individual cells. Specifically, the n‐type conjugated polyelectrolyte p(cNDI‐gT2) exhibits a reduction potential window between −0.1 and −0.8 V (vs Ag/AgCl), thereby driving thermodynamically favored electron transfer in both directions across the abiotic‐biotic interface that involves the outer membrane cytochromes and flavins of Shewanella oneidensis MR‐1. Electrochemical tests show that injection from an external electrode into Shewanella oneidensis MR‐1 is enabled at negative potentials (−0.6 V), while electron extraction is possible at positive potentials (0.2 V). Relative to controls, the biohybrid shows a sixfold increase in biocurrent generation and a 35‐fold increase in current uptake for the bioelectrosynthesis of succinate from fumarate. This demonstrated abiotic‐biotic synergy provides new strategies for designing multifunctional biohybrids. [ABSTRACT FROM AUTHOR]

Electromicrobiology is an emerging field investigating and exploiting the interaction of microorganisms with insoluble electron donors or acceptors. Some of the most recently categorized electroactive microorganisms became of interest to sustainable bioengineering practices. However, laboratories worldwide typically maintain electroactive microorganisms on soluble substrates, which often leads to a decrease or loss of the ability to effectively exchange electrons with solid electrode surfaces. In order to develop future sustainable technologies, we cannot rely solely on existing lab-isolates. Therefore, we must develop isolation strategies for environmental strains with electroactive properties superior to strains in culture collections. In this article, we provide an overview of the studies that isolated or enriched electroactive microorganisms from the environment using an anode as the sole electron acceptor (electricity-generating microorganisms) or a cathode as the sole electron donor (electricity-consuming microorganisms). Next, we recommend a selective strategy for the isolation of electroactive microorganisms. Furthermore, we provide a practical guide for setting up electrochemical reactors and highlight crucial electrochemical techniques to determine electroactivity and the mode of electron transfer in novel organisms.

Electromicrobiology is an emerging field investigating and exploiting the interaction of microorganisms with insoluble electron donors or acceptors. Some of the most recently categorized electroactive microorganisms became of interest to sustainable bioengineering practices. However, laboratories worldwide typically maintain electroactive microorganisms on soluble substrates, which often leads to a decrease or loss of the ability to effectively exchange electrons with solid electrode surfaces. In order to develop future sustainable technologies, we cannot rely solely on existing lab-isolates. Therefore, we must develop isolation strategies for environmental strains with electroactive properties superior to strains in culture collections. In this article, we provide an overview of the studies that isolated or enriched electroactive microorganisms from the environment using an anode as the sole electron acceptor (electricity-generating microorganisms) or a cathode as the sole electron donor (electricity-consuming microorganisms). Next, we recommend a selective strategy for the isolation of electroactive microorganisms. Furthermore, we provide a practical guide for setting up electrochemical reactors and highlight crucial electrochemical techniques to determine electroactivity and the mode of electron transfer in novel organisms.

Extracellular electron transfer (EET) between microbes and iron minerals, and syntrophically between species, is a widespread process affecting biogeochemical cycles and microbial ecology. The distribution of this capacity among microbial taxa, and the thermodynamic controls on EET in complex microbial communities, are not fully known. Microbial electrochemical cells (MXCs), in which electrodes serve as the electron acceptor or donor, provide a powerful approach to enrich for organisms capable of EET and to study their metabolism. We used MXCs coupled with genome-resolved metagenomics to investigate the capacity for EET in microorganisms present in a well-studied aquifer near Rifle, CO. Electroactive biofilms were established and maintained for almost 4 years on anodes poised mostly at -0.2 to -0.25 V vs. SHE, a range that mimics the redox potential of iron-oxide minerals, using acetate as the sole carbon source. Here we report the metagenomic characterization of anode-biofilm and planktonic microbial communities from samples collected at timepoints across the study period. From two biofilm and 26 planktonic samples we reconstructed draft-quality and near-complete genomes for 84 bacteria and 2 archaea that represent the majority of organisms present. A novel Geobacter sp. with at least 72 putative multiheme c-type cytochromes (MHCs) was the dominant electrode-attached organism. However, a diverse range of other electrode-associated organisms also harbored putative MHCs with at least 10 heme-binding motifs, as well as porin-cytochrome complexes and e-pili, including Actinobacteria, Ignavibacteria, Chloroflexi, Acidobacteria, Firmicutes, Beta- and Gammaproteobacteria. Our results identify a small subset of the thousands of organisms previously detected in the Rifle aquifer that may have the potential to mediate mineral redox transformations.

Research regarding microbial fuel cells has been stimulated to reduce the operating costs and energy consumption of conventional wastewater treatment, and increase its profitability. However, these devices are challenging to study due to their complexity and sensitivity to both internal and external factors. Artificial intelligence (AI) has been used to analyze microbial fuel cells as an effective alternative to the use of mathematical models, which are still in development. In this study, the main goals were to perform the first bibliometric analysis of AI applied to microbial fuel cell research and to find the most popular algorithms used to date. Using the Web of Science database, a total of 102 articles published between 1999 and 2022 were retrieved. The cumulative number of articles has greatly increased over the past 10 years. About 55% were contributed by researchers from China and USA, leading among 20 countries. Some 50 algorithms were used, with principal component analysis and feed-forward neural networks being the most popular used to study and optimize microbial fuel cells. HIGHLIGHTS The first bibliometric analysis of applied to microbial fuel cell research was performed.; The number of publications has grown exponentially since 2013.; 102 articles were published between 1999 and 2022.; 50 AI algorithms have been used in microbial fuel cell research.; The most popular algorithms are principal component analysis and feed-forward neural networks.;