Acetate-fed Microbial Fuel Cells Research Articles

Evolution and interaction of microbial communities in mangrove microbial fuel cells and first description of Shewanella fodinae as electroactive bacterium

Understanding exoelectrogenic bacteria mechanisms and their interactions in complex biofilm is critical for the development of microbial fuel cells (MFCs). In this article, assumptions concerning the benefits of the complex sediment microbial community for electricity production were explored with both the complex microbial community and isolates identified as Shewanella. Analysis of the microbial community revealed a strong influence of the sediment community on anodes and electrolytes compared to that of only water. Moreover, while Pelobacteraceae-related genera were dominant in our MFCs instead of Desulfuromonas and Geobacter as usually reported, the electroactive Shewanella algae and Shewanella fodinae were isolated and cultivated from the anodic biofilm. S. fodinae, described for the first time as an electroactive bacterium to the best of our knowledge, led to a maximal current density of 3.6 A/m2 set as 0.3 V/SCE in a three-electrode set-up fed with lactate. S. algae, in a complex medium containing several available substrates, showed several preferential oxidative behaviors including a diauxic behavior. In pure culture and under our conditions, S. fodinae and S. algae were not able to use acetate as a sole electron donor. However, their presence in our acetate-fed MFCs and the adaptive behavior of S. algae hint a syntrophic interaction between the bacteria to optimize the use of the substrate in a complex environment.

Enumeration of exoelectrogens in microbial fuel cell effluents fed acetate or wastewater substrates

Effluents from well-acclimated microbial fuel cells (MFCs) have been widely used as inocula to start up new MFC reactors. However, the actual cell concentrations and cell viability of exoelectrogens in these MFC effluents have not been well examined. In this study, concentrations of exoelectrogens in the effluent from acetate- or wastewater-fed MFCs were examined using a quantitative polymerase chain reaction (qPCR) method specific for Geobacter spp. that are usually the dominant genus in MFCs, and a non-specific WO3 nanocluster/most probable number (WO3/MPN) method for enumeration of viable exoelectrogens. Geobacter spp. concentrations in acetate-fed MFC effluents based on qPCR were 1.3 ± 0.2 × 108 cells/mL, slightly higher than those in the wastewater-fed MFC effluents (9.3 ± 3.5 × 107 cells/mL). However, exoelectrogen cell counts using the WO3/MPN method were several orders of magnitude lower for both MFC effluents (1.1 ± 0.3 × 104 cells/mL for acetate-fed; 1.4 ± 0.3 × 105 cells/mL for wastewater-fed). Live/dead cell staining suggested that most cells (85 %) in the effluents were inactive or dead, which could partly explain the lower numbers using the WO3/MPN method. These results suggest that both acetate- and wastewater-fed MFC effluents contain high numbers of Geobacter spp. although a high percentage of cells are not viable.

Hydrogen and electrical energy co-generation by a cooperative fermentation system comprising Clostridium and microbial fuel cell inoculated with port drainage sediment

This research work has succeeded in recovering energy from glucose by generating H2 with the aid of a Clostridium beijerinckii strain and obtaining electrical energy from compounds present in the H2 fermentation effluent in a microbial fuel cell (MFC) seeded with native port drainage sediment. In the fermentation step, 49.5% of the initial glucose concentration (56 mmol/L) was used to produce 104 mmol/L H2; 5, 33, 3, and 1 mmol/L acetate, butyrate, lactate, and ethanol also emerged, respectively. MFC tests by feeding the anodic compartment with acetate, butyrate, lactate (individually or as a mixture), or the H2 fermentation effluent provided power density values ranging between 0.6 and 1.2 W/m2. Acetate furnished the highest power density with a nanowire-rich biofilm despite the lowest anode bacterial concentration (1012 16S gene copies/g of sediment). Non-conventional exoelectrogenic microbial communities were observed in the acetate-fed MFC; e.g., Pseudomonadaceae (Pseudomonas) and Clostridia (Acidaminobacter, Fusibacter).

Bioelectricity generation using microalgal biomass as electron donor in a bio-anode microbial fuel cell

In this study, microalgal biomass waste (Chlorella regularis) was treated while simultaneously producing bioelectricity in a microbial fuel cell (MFC). Algal biomass was the sole electron donor and was enriched with easily biodegradable proteins (46%) and carbohydrates (22%). The generated power density was 0.86 W/m2 and the columbic efficiency reached ∼61.5%.The power generation could be further increased to 1.07 W/m2 by using a biomass waste concentration enhancement strategy with maximum chemical oxygen demand (COD) removal of ∼65.2%. Via direct comparison, the power generation and COD removal capability of the algal-fed MFC was close to that of the commercial acetate-fed MFC. The algae-fed MFC presented superior electrochemical characteristics that were attributed to the complicated composition of the biomass anolyte. It possessed a multiple anode respiring bacterial group and diverse microbial community. Hence, this study provides a new strategy for the utilization of microalgal biomass as a bioresource.

Power densities and microbial communities of brewery wastewater-fed microbial fuel cells according to the initial substrates.

Single-chamber microbial fuel cells (MFCs) acclimated with glucose, butyrate, propionate, acetate, and a mixture of the four were operated with brewery wastewater (BWW) under a fed-batch mode. Glucose-fed MFC (GW-MFC) showed the highest maximum power density (PDmax) of 1,519mW/m(2), followed in order by acetate-fed MFC (AW-MFC), mixed substrates-fed MFC (MW-MFC), butyrate-fed MFC (BW-MFC), and propionate-fed MFC (PW-MFC). After changing to BWW, power production was decreased for all MFCs. MFC acclimated with glucose showed the highest PDmax of 890±12 mW/m(2), followed in order by MW-MFC, AW-MFC, BW-MFC, and PW-MFC. The PDmax in BWW-MFC, which was acclimated and operated with BWW, of 552mW/m(2) was less than that of GW-MFC and MW-MFC but more than that of AW-MFC, BW-MFC, and PW-MFC. MFCs with fermentable substrates were less affected by the BWW. Gammaproteobacteria, including Pseudomonas sp., Acinetobacter sp. and Xanthomonas axonopodis, were found in all MFCs with pure substrates and Rubrivivax benzoatilyticus, thiobacillus sp. and Denitratisoma oestradiolicum belonging to Betaproteobacteria were newly detected in all MFCs when the substrate was changed to BWW.

Microbial community in microbial fuel cell (MFC) medium and effluent enriched with purple photosynthetic bacterium (Rhodopseudomonas sp.).

High power densities have been obtained from MFC reactors having a purple color characteristic of Rhodopseudomonas. We investigated the microbial community structure and population in developed purple MFC medium (DPMM) and MFC effluent (DPME) using 16S rRNA pyrosequencing. In DPMM, dominant bacteria were Comamonas (44.6%), Rhodopseudomonas (19.5%) and Pseudomonas (17.2%). The bacterial community of DPME mainly consisted of bacteria related to Rhodopseudomonas (72.2%). Hydrogen oxidizing bacteria were identified in both purple-colored samples: Hydrogenophaga and Sphaerochaeta in the DPMM, and Arcobacter, unclassified Ignavibacteriaceae, Acinetobacter, Desulfovibrio and Wolinella in the DPME. The methanogenic community of both purple-colored samples was dominated by hydrogenotrophic methanogens including Methanobacterium, Methanobrevibacter and Methanocorpusculum with significantly lower numbers of Methanosarcina. These results suggeste that hydrogen is actively produced by Rhodopseudomonas that leads to the dominance of hydrogen consuming microorganisms in both purple-colored samples. The syntrophic relationship between Rhodopseudomonas and hydrogenotrophic microbes might be important for producing high power density in the acetate-fed MFC under light conditions.

Electricity generation and microalgae cultivation in microbial fuel cell using microalgae-enriched anode and bio-cathode

In this study, a microbial fuel cell (MFC) was developed to treat waste, produce electricity and to grow microalgae simultaneously. Dead microalgae biomass (a potential pollution vector in streams) was used as a substrate at anode. CO2 generated at anode was used to grow freshwater microalgae at cathode. The performance of microalgae-fed MFC was compared with acetate-fed MFC. The maximum power density of 1926±21.4mW/m2 (8.67±0.10W/m3, at Rext=100Ω) and Coulombic efficiency (CE) of 6.3±0.2% were obtained at 2500mg COD/L of microalgae powder (0.5g/L). Microalgae captured CO2 (5–14%, v/v) to produce a biomass concentration of 1247±52mg/L. However, microalgae could not grow in acetate-fed (0.5g/L) MFC (acetate-control) and without anodic CO2 supplying MFC (CO2-control).

Establishing a core microbiome in acetate-fed microbial fuel cells

Establishing a core microbiome is the first step in understanding and subsequently optimizing microbial interactions in anodic biofilms of microbial fuel cells (MFCs) for increased power, efficiency, and decreased start-up times. In the present study, we used 454 pyrosequencing to demonstrate that a core anodic community would consistently emerge over a period of 4years given similar conditions. The development and variation across reactor designs of these communities was also explored. The core members present in all high-power generating biofilms were Geobacter, Aminiphilus, Sedimentibacter, Acetoanaerobium, and Spirochaeta, accounting for 72 ± 9% of all genera. Aminiphilus spp., member of the Synergistetes phylum was present at higher abundances than previously reported in any other ecological studies. Results suggest a stable core microbiome in acetate-fed MFCs on both phylogenetic and functional levels.

Can microbial fuel cells be an effective mitigation strategy for methane emissions from paddy fields?

Microbial fuel cells (MFCs) are bioelectrochemical systems able to generate electricity from wetland soils, including paddies, exploiting the microbial decomposition of organic matter. Additionally, MFCs can also be applied as a novel mitigation strategy for emissions of methane (CH4) from paddy fields. The MFC efficiency in reducing CH4 fluxes is still poorly understood, and it is here investigated via a one-dimensional process-based model that simulates the vertical and temporal dynamics of the chemical compounds affecting CH4 fate within paddy soil. The DOC oxidation rate of MFC is modeled assuming a zero-order kinetics proportional to the generated electricity and different anode depths and current densities are tested. By assuming current densities presently achieved in paddies, MFCs are able to reduce up to −27.9%, −16.7%, and −22.0% of daily minimum, daily maximum, and total CH4 emissions, respectively. Moreover, CH4 reductions are even higher (up to −28.1%, −24.1%, and −26.5%) if we assume 5% of the current density developed on laboratory acetate-fed MFC. The system shows a limiting effect of transport processes on the mitigation of CH4 emissions at high current density. In order to maximize the reduction of CH4 emissions, simulation results suggest to place the anode in the middle portion of the superficial layer of paddy soil. The findings demonstrate the need to further investigate and develop this new technology for field-scale applications.

Acetate oxidation by syntrophic association between Geobacter sulfurreducens and a hydrogen-utilizing exoelectrogen

Anodic microbial communities in acetate-fed microbial fuel cells (MFCs) were analyzed using stable-isotope probing of 16S rRNA genes followed by denaturing gradient gel electrophoresis. The results revealed that Geobacter sulfurreducens and Hydrogenophaga sp. predominated in the anodic biofilm. Although the predominance of Geobacter sp. as acetoclastic exoelectrogens in acetate-fed MFC systems has been often reported, the ecophysiological role of Hydrogenophaga sp. is unknown. Therefore, we isolated and characterized a bacterium closely related to Hydrogenophaga sp. (designated strain AR20). The newly isolated strain AR20 could use molecular hydrogen (H2), but not acetate, with carbon electrode as the electron acceptor, indicating that the strain AR20 was a hydrogenotrophic exoelectrogen. This evidence raises a hypothesis that acetate was oxidized by G. sulfurreducens in syntrophic cooperation with the strain AR20 as a hydrogen-consuming partner in the acetate-fed MFC. To prove this hypothesis, G. sulfurreducens strain PCA was cocultivated with the strain AR20 in the acetate-fed MFC without any dissolved electron acceptors. In the coculture MFC of G. sulfurreducens and strain AR20, current generation and acetate degradation were the highest, and the growth of strain AR20 was observed. No current generation, acetate degradation and cell growth occurred in the strain AR20 pure culture MFC. These results show for the first time that G. sulfurreducens can oxidize acetate in syntrophic cooperation with the isolated Hydrogenophaga sp. strain AR20, with electrode as the electron acceptor.

Enhanced Electricity Production by Use of Reconstituted Artificial Consortia of Estuarine Bacteria Grown as Biofilms

Microbial fuel cells (MFCs) can convert organic compounds directly into electricity by catalytic oxidation, and although MFCs have attracted considerable interest, there is little information on the electricity-generating potential of artificial bacterial biofilms. We have used acetate-fed MFCs inoculated with sediment, with two-chamber bottles and carbon cloth electrodes to deliver a maximum power output of ~175 mW · m(-2) and a stable power output of ~105 mW · m(-2). Power production was by direct transfer of electrons to the anode from bacterial consortia growing on the anode, as confirmed by cyclic voltammetry (CV) and scanning electron microscopy (SEM). Twenty different species (74 strains) of bacteria were isolated from the consortium under anaerobic conditions and cultured in the laboratory, of which 34% were found to be exoelectrogens in single-species studies. Exoelectrogenesis by members of the genera Vibrio , Enterobacter , and Citrobacter and by Bacillus stratosphericus was confirmed, by use of culture-based methods, for the first time. An MFC with a natural bacterial consortium showed higher power densities than those obtained with single strains. In addition, the maximum power output could be further increased to ~200 mW · m(-2) when an artificial consortium consisting of the best 25 exoelectrogenic isolates was used, demonstrating the potential for increased performance and underlying the importance of artificial biofilms for increasing power output.

Microbial Communities and Electrochemical Performance of Titanium-Based Anodic Electrodes in a Microbial Fuel Cell

Four types of titanium (Ti)-based electrodes were tested in the same microbial fuel cell (MFC) anodic compartment. Their electrochemical performances and the dominant microbial communities of the electrode biofilms were compared. The electrodes were identical in shape, macroscopic surface area, and core material but differed in either surface coating (Pt- or Ta-coated metal composites) or surface texture (smooth or rough). The MFC was inoculated with electrochemically active, neutrophilic microorganisms that had been enriched in the anodic compartments of acetate-fed MFCs over a period of 4 years. The original inoculum consisted of bioreactor sludge samples amended with Geobacter sulfurreducens strain PCA. Overall, the Pt- and Ta-coated Ti bioanodes (electrode-biofilm association) showed higher current production than the uncoated Ti bioanodes. Analyses of extracted DNA of the anodic liquid and the Pt- and Ta-coated Ti electrode biofilms indicated differences in the dominant bacterial communities. Biofilm formation on the uncoated electrodes was poor and insufficient for further analyses. Bioanode samples from the Pt- and Ta-coated Ti electrodes incubated with Fe(III) and acetate showed several Fe(III)-reducing bacteria, of which selected species were dominant, on the surface of the electrodes. In contrast, nitrate-enriched samples showed less diversity, and the enriched strains were not dominant on the electrode surface. Isolated Fe(III)-reducing strains were phylogenetically related, but not all identical, to Geobacter sulfurreducens strain PCA. Other bacterial species were also detected in the system, such as a Propionicimonas-related species that was dominant in the anodic liquid and Pseudomonas-, Clostridium-, Desulfovibrio-, Azospira-, and Aeromonas-related species.

The effect of real-time external resistance optimization on microbial fuel cell performance

This work evaluates the impact of the external resistance (electrical load) on the long-term performance of a microbial fuel cell (MFC) and demonstrates the real-time optimization of the external resistance. For this purpose, acetate-fed MFCs were operated at external resistances, which were above, below, or equal to the internal resistance of a corresponding MFC. A perturbation/observation algorithm was used for the real-time optimal selection of the external resistance. MFC operation at the optimal external resistance resulted in increased power output, improved Coulombic efficiency, and low methane production. Furthermore, the efficiency of the perturbation/observation algorithm for maximizing long-term MFC performance was confirmed by operating an MFC fed with synthetic wastewater for over 40 days. In this test an average Coulombic efficiency of 29% was achieved.

Influence of External Resistance on Electrogenesis, Methanogenesis, and Anode Prokaryotic Communities in Microbial Fuel Cells

The external resistance (R(ext)) of microbial fuel cells (MFCs) regulates both the anode availability as an electron acceptor and the electron flux through the circuit. We evaluated the effects of R(ext) on MFCs using acetate or glucose. The average current densities (I) ranged from 40.5 mA/m(2) (9,800 Ω) to 284.5 mA/m(2) (150 Ω) for acetate-fed MFCs (acetate-fed reactors [ARs]), with a corresponding anode potential (E(an)) range of -188 to -4 mV (versus a standard hydrogen electrode [SHE]). For glucose-fed MFCs (glucose-fed reactors [GRs]), I ranged from 40.0 mA/m(2) (9,800 Ω) to 273.0 mA/m(2) (150 Ω), with a corresponding E(an) range of -189 to -7 mV. ARs produced higher Coulombic efficiencies and energy efficiencies than GRs over all tested R(ext) levels because of electron and potential losses from glucose fermentation. Biogas production accounted for 14 to 18% of electron flux in GRs but only 0 to 6% of that in ARs. GRs produced similar levels of methane, regardless of the R(ext). However, total methane production in ARs increased as R(ext) increased, suggesting that E(an) might influence the competition for substrates between exoelectrogens and methanogens in ARs. An increase of R(ext) to 9,800 Ω significantly changed the anode bacterial communities for both ARs and GRs, while operating at 970 Ω and 150 Ω had little effect. Deltaproteobacteria and Bacteroidetes were the major groups found in anode communities in ARs and GRs. Betaproteobacteria and Gammaproteobacteria were found only in ARs. Bacilli were abundant only in GRs. The anode-methanogenic communities were dominated by Methanosaetaceae, with significantly lower numbers of Methanomicrobiales. These results show that R(ext) affects not only the E(an) and current generation but also the anode biofilm community and methanogenesis.

Novel Electrochemically Active Bacterium Phylogenetically Related to Arcobacter butzleri , Isolated from a Microbial Fuel Cell

Exoelectrogenic bacteria are organisms that can transfer electrons to extracellular insoluble electron acceptors and have the potential to be used in devices such as microbial fuel cells (MFCs). Currently, exoelectrogens have been identified in the Alpha-, Beta-, Gamma- and Deltaproteobacteria, as well as in the Firmicutes and Acidobacteria. Here, we describe use of culture-independent methods to identify two members of the genus Arcobacter in the Epsilonproteobacteria that are selectively enriched in an acetate-fed MFC. One of these organisms, Arcobacter butzleri strain ED-1, associates with the electrode and rapidly generates a strong electronegative potential as a pure culture when it is supplied with acetate. A mixed-community MFC in which approximately 90% of the population is comprised of the two Arcobacter species generates a maximal power density of 296 mW/liter. This demonstration of exoelectrogenesis by strain ED-1 is the first time that this property has been shown for members of this genus.

Evaluation of energy-conversion efficiencies in microbial fuel cells (MFCs) utilizing fermentable and non-fermentable substrates

We established the first complete electron-equivalent balances in microbial fuel cells (MFCs) fed with non-fermentable (acetate) and fermentable (glucose) electron donors by experimentally quantifying current, biomass, residual organic compounds, H 2, and CH 4 gas. The comparison of the two donors allowed us to objectively evaluate the diversion of electron flow to non-electricity sinks for fermentable donors, leading to different behaviors in energy-conversion efficiency (ECE) and potential efficiency (PE). Electrical current was the most significant electron sink in both MFCs, being 71% and 49%, respectively, of the initial COD applied. Biomass and residual organic compounds, the second and third greatest sinks, respectively, were greater in the glucose-fed MFC than in the acetate-fed MFC. We detected methane gas only in the glucose-fed MFC, and this means that anode-respiring bacteria (ARB) could out-compete acetoclastic methanogens. The ECE was 42% with acetate, but was only 3% with glucose. The very low ECE for glucose was mostly due to a large increase of the anode potential, giving a PE of only 6%. Although the glucose-fed MFC had the higher biomass density on its anode, it had a very low current density, which supports the fact that the density of ARB was very low. This led to slow kinetics for electron transfer to the anode and accentuated loss due to the substrate-concentration gradient in the anode-biofilm. The large drop of PE with low current, probably caused by a low ARB density and electron (e −) donor concentration, resulted in a poor maximum power density (9.8 mW/m 2) with glucose. In contrast, PE reached 59% along with high current for acetate and the maximum power density was 360 mW/m 2.