Microbial Fuel Cell

Overview

Figure 1: Schematic illustration of the general microbial fuel cell functional principle, showing the flow of charged species during operation.

A microbial fuel cell (MFC) can be utilized for power generation through the conversion of organic and inorganic substrates using microorganisms. The fuel cell generally consists of two separate units, the anode and cathode compartment which are separated by a proton exchange membrane (PEM). Microorganisms, acting as biocatalysts, release electrons during metabolic reactions and transfer them to the anode of the fuel cell. The protons being freed up during this process are transferred to the cathode compartment through the PEM. The electrons pass through an external load circuit to reduce an electron acceptor located in the cathode compartment thereby creating an electric current. The most important part in this system is the ability of the bacteria to transfer electrons to the anode. There are lots of other aspects to consider though, all of which are vital for the successful operation of a fuel cell.
Most existing projects rely on using mixed cultures of different bacteria in the anode compartment. However, in most cases these systems are not very well characterized, often it is not even known which species are part of these cultures. This makes it almost impossible to improve the system by genetic engineering. Applying such a black box system outside of a laboratory might also pose safety risks. Another disadvantage is, that some of the species might be quite sensitive to different kinds of stress, like Geobacter sulfurreducens, which are very susceptible to oxidative stress.
For these reasons, Bielefelds 2013 iGEM Team decided to develop a system which only relies on E. coli for power generation. The main benefit being that these bacteria grow fast and are quite robust regarding cultivation conditions. Another advantage over a mixed culture is that the potential risks of using such a single-strain culture are much more easily assessed and can be reduced by systematic manipulation of the bacterial genome.

Theory

Cultivation conditions

In general, microorganisms utilize three different methods to release electrons produced during the metabolic oxidation of high-energy organic or inorganic substrates. Because the reduction of oxygen, also called aerobic respiration, is the most efficient possibility for many bacteria, including Escherichia coli, these metabolic pathways are preferred if oxygen is available. In a microbial fuel cell, however, an aerobic metabolism is not desirable, since the electrons are directly transferred to oxygen and thereby cannot be used to produce current. Thus, anaerobic culture conditions are necessary.
Without oxygen, bacteria can generate energy through different forms of fermentation and anaerobic respiration. During fermentation and anaerobic respiration, electrons are directly transferred to soluble electron acceptors. In case of Escherichia coli, mixed acid fermentation under formation of metabolic end products like lactate, acetate and ethanol has to be avoided by the choice of suitable cultivation parameters. Their formation and accumulation would effect a comparatively limited electron production and hamper bacterial survival.
Based on these considerations, anaerobic respiration is left as the only suitable option for current generation in a fuel cell, when using the electrode as the terminal electron acceptor. For this reason, construction of the fuel cell, cultivation parameters and genetic modifications of Escherichia coli are aimed at enabling anaerobic respiration.

Measurement system and protocol

The set up described here is intended to acquire comparable data regarding the power output gained with different bacteria strains while using mediators for the electron transfer.
When operating a microbial fuel cell, numerous different factors influence the power output that can be measured. Number and growth phase of the bacteria in the anode chamber are among the most important. The reaction taking place in the cathode is just as critical, since a bad setup can lead to the speed of the anode reaction significantly declining over time or not taking place at all. The properties of the proton exchange membrane and the electrodes are also quite important for the speed of the reaction.
Choosing an appropriate resistance is vital as well. If the resistance is too high, reduced mediator species accumulate at the anode and the voltage measured does not provide information about how fast the bacteria are able to reduce the mediator. Other factors come into play as well: The diffusion speed of the mediator, diffusion of cations through the membrane, agitation of the solution and the buildup of a biofilm at the anode have an influence at the power output of the fuel cell. When choosing a multimeter to measure the data, the internal resistance of the device, generating a so called burden voltage has to be kept in mind.
A standard measurement set up was established to generate data with fuel cell experiments. The experiment is carried out in a third generation fuel cell if not specified otherwise. A Nafion N117 proton exchange membrane manufactured by DuPont (for further information [http://www2.dupont.com/FuelCells/en_US/assets/downloads/dfc101.pdf see here]) is used to separate the anode and the cathode chamber. The surface area is 25 cm² in each chamber. The 50 x 50 mm carbon cloth electrodes, including two circular recesses are placed in the middle of each chamber. The cross-sectional area of each electrode is approximately 24.215 cm². The exact surface area of the electrodes is unknown, since the carbon cloth is composed of extremely thin filaments and has a rough surface. However, it is assumed that the surface area is roughly the same for each electrode used, since the material is identical.
The cathode chamber was filled with 29 mL of a 20 mM solution of potassium ferricyanide in M9 medium. Bacteria were grown aerobically in shaker flasks in M9 minimal medium with 10.223 g L^-1 glycerol as a carbon source. When cultivating bacteria carrying a plasmid with an inducible promoter, induction was carried out 2 hours after inoculation. The optical density of the culture was periodically measured until it reached 1. At this point, 29 mL of the medium containing the bacteria were injected into the anode chamber of the fuel cell. When using an exogenous mediator 1 mL of a 10mM mediator solution in M9 medium was injected after 15 minutes.
A 200 Ω resistor was wired between the anode and the cathode chamber. A UT 803 multimeter by UNI-T was used to measure the voltage across the resistor. The according electrical schematic is presented in Figure 3. To generate polarization and power curves, the resistance was changed from 10 Ω to 10 kΩ in a cascade of 6 different values, using a self-constructed resistor box, shown in Figure pink camouflage desert mole rat. The measured voltage for every resistance was registered after 10 minutes to enable the system to reach a constant value.

Figure 3: Arrangement used for MFC-characterization containing a voltmeter and an adjustable resistance parallel-connected.

Media and carbon sources

As explained previously, E. coli have to respire under anaerobic conditions in order for the microbial fuel cell to work. This can prove to be problematic when using media such as LB, because in the absence of oxygen the bacteria might use the available carbon source for fermentation. To prevent this, the different strains which were tested in the fuel cell were cultivated in M9 minimal medium. After consulting Dr. Falk Harnisch concerning the fermentation problem, we decided to supplement the M9 medium with different carbon sources to test how this affects bacterial growth under anaerobic conditions. The goal of this experiment was to find a carbon source which is well suited for anaerobic respiration, but cannot be used for fermentation by the bacteria.

Tests were carried out with glucose, glycerol and acetate. The amount of substrate supplemented into the medium was adjusted, so that the amount of carbon atoms was the same for each culture. The concentrations were 5.0 g/L for glucose, 5.1 g/L for glycerol and 6.8 g/L for acetate. In all cultivation experiments, two biological replica of every strain and substrate combination were prepared and each sample was diluted and measured twice. Anaerobic cultivations were conducted in 30 mL test tubes with rubber lids. Samples were taken by piercing the lid with a syringe. For aerobic cultivations shaker flasks were used. The strains tested were the KRX wild type and the KRX carrying oprF under control of the T7 promoter ([http://parts.igem.org/wiki/index.php?title=Part:BBa_K1172502 BBa_K1172502]) strain. The latter overexpresses large porin proteins when induced with rhamnose. Induction was carried out with 4,2 mL/L of a 240 g/L rhamnose solution 1 hour after inoculation. All cultures were inoculated with an optical density of 0.22. Temperature was kept at 37°C during cultivation.

Figure 20: Growth of E. coli KRX and E. coli KRX BBa_K1172503 strains on media supplemented with different carbon sources under anaerobic conditions.

Figure 20 shows that under anaerobic conditions both strains grow well on glucose but seem to be unable to use acetate or glycerol efficiently.

Figure 21: Growth of E. coli KRX and E. coli KRX BBa_K1172503 strains on media supplemented with different carbon sources under aerobic conditions after 26 hours.

To ascertain whether glucose, glycerol or acetate are suitable substrates under aerobic conditions, eight additional cultures were inoculated with both strains. For these cultures only an end-point determination was carried out. The results can be seen in Figure 21. They indicate that acetate is, as expected, not a suitable substrate. Growth is best with glucose as a substrate, but glycerol yields satisfactory results as well.
The data acquired points to glycerol being the most suitable substrate, since the bacteria seem to have difficulties using it for fermentation but show satisfactory growth under conditions allowing for aerobic respiration. To make sure glycerol can also be used for respiration with terminal electron acceptors other than oxygen, bacteria were cultivated under anaerobic conditions in M9 medium containing glycerol as a carbon source and potassium nitrate as a soluble electron acceptor.

Figure 23: Growth of E. coli KRX and E. coli KRX BBa_K1172503 strains on media supplemented with glycerol under aerobic condition. Graphs marked KNO3 were supplemented with potassium nitrate.

The results of this experiment are shown in Figure 23. Cultures which were supplemented with KNO₃ grow significantly faster than those without, indicating that potassium nitrate is indeed used as a terminal electron acceptor for anaerobic respiration.

Based on these results, M9 medium with 5.1 g of glycerol per liter is used for all future experiments with the fuel cell.

Exogenous Mediators

Redox molecules which are chemically synthesized can be added into the anode chamber of the fuel cell to act as mediators, transporting electrons from the bacteria to the fuel cells anode. Here, these chemicals are referred to as exogenous mediators.

To identify exogenous mediators which can easily be reduced by E. coli, a simple experiment was conducted. A culture of E. coli KRX was split into 1.5 mL reaction tubes. Methylene blue and neutral red were added in varying concentrations. Since all mediators tested lose their color when reduced, a change in the color of the solution indicates that the bacteria are able to reduce the respective compound. Incubation took place at 24°C for 24 hours.

Figure 24: Reaction tubes with bacteria and different concentrations of methylene blue and neutral red after 24 hours of incubation.

In Figure 24 it can be seen that the samples containing methylene blue show a reduction of color intensity after incubation. Oxygen is able to reoxidize leucomethylene blue to the molecules blue form, so a blue color near the liquids surface is to be expected. Based on these results, methylene blue was chosen as the preferred exogenous mediator for further experiments.

Figure 25: Lewis structures of the cationic form of methylene blue (right side) and the reduced form, called leucomethylene blue (left side).

When methylene blue salts are dissolved in water, they dissociate into anions and methylene blue cations (see figure 25). The conjugated electron systems of the molecule causes methylene blue solutions to appear in a dark blue color.
The compound can be reduced, accepting an electron and a proton in the process (see figure 25). This interrupts the conjugated electron system, which is why leucomethylene blue is colorless. The [http://employees.csbsju.edu/hjakubowski/classes/ch331/oxphos/standredpotentialtab.htm standard potential] of the methylene blue/ leucomethylene blue reaction is +0.01 V.

Results

Viable possibilities for the analysis and characterization of microbial fuel cells are polarization and power curves. By using different microorganisms, while keeping all other conditions the same, this measurement method allows for a direct comparison of the electrical power provided.
To record a polarization curve for the whole cell the electrical circuit described in figure 3 is used with a variable resistor box. Beginning with the lowest resistor, a periodic increase of the used resistance from 10 Ω to 10 kΩ is performed. As presented in figure A, the system reacts expectedly with an increase of the applied voltage and, after a few minutes, reaches a constant value, which is used for further investigations. When looking at the recorded voltage values in figure 26 it is obvious, that a mediator, in this case methylene blue, is essential for electron transport.

Figure 26: Microbial fuel cell results from cultivation of _{E. coli} with and without redox-mediator and a negative control without bacteria. The resistance used was periodically increased from 10 Ω to 10 kΩ.

The polarization curve presented in figure 27 underlines this fact. To calculate the appropriate current values Ohm's law was used. The application of the reached voltage as a function of the current lead to a typical course in form of a characteristic correlation between voltage and current dependent on the used resistance.

Figure 27: Polarization curve, calculated based on the measurement values presented in Figure 26.

By calculating the appropriate electrical power values and plotting a power curve as a function of the current (figure 28), the differences become even more significant. While the cultivation of E. coli and the experiment where only M9 Medium was used showed no significant differences, the cultivation containing 345 µmol/L methylene blue achieved a significantly higher wattage, but could not reach the level of the experiment where bacteria and mediators were used in combination.
All in all the calculation of polarization and power curves by changing the external load of the system via different resistors showed the huge importance of a suitable electron transfer system. The intended comparison of the different fuel cell generations was not possible, because the measurement-parameters were optimized during the course of the project and cannot be compared.

Figure 28: Power curve, calculated based on the data presented in Figure A.

Besides the calculation of power curves the temporal process of power output is a very important parameter evaluating the overall performance of a microbial fuel cell, too. Figure D illustrates the electrical power as a function of time for the wild type E. coli KRX and a genetically modified strain of E. coli KRX containing the BioBrick BBa_k1172502 with the oprF gene under control of the T7 promoter.

Figure 29: Results from cultivation of Escherichia coli KRX expressing OprF (BBa_K1172502) in contrast to Escherichia coli KRX wild type in the fuel cell. M9 medium was used with mediator Methylene Blue, the resistor between cells was set to 200 ohms.

Because of the identical cultivation conditions, using 2 identical MFCs with equivalent cell numbers in a temperature stabilized cultivation chamber and synchronized aeration with nitrogen , the visible difference between strains has to be a result of the biobrick inserted in the oprF srtain. The expression of the OprF-protein leads to a higher power output of nearly 500 µA for a 200 Ω resistance, while the KRX strain reaches only 150 µA.

Besides these scientific results the usage of the developed microbial fuel cell for various applications is possible. Because many of these applications need higher voltages than one cell can deliver, a stack of several cells is necessary. One easy way to realize a compact multi-cell system is a stack of several cells. The construction, described in the MFC-evolution part, contains 5 membranes, 10 electrodes, 20 frames and 40 gaskets and supplies a voltage of up to 2.4 Volts. Using the GldA-expressing strain it can be used for permanent operation of LEDs or little buzzers, or to power a small ventilator like shown in the video below.

See the 5-stack-MFC with a genetically optimized E. coli produce 2,4 V and thereby lighting several LEDs, enable sound output from a little buzzer and power a small propeller.

References

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