The Effect of Bismuth and Tin on Methane and Acetate Production in a Microbial Electrosynthesis Cell Fed with Carbon Dioxide.

This study investigates the impacts of bismuth and tin on the production of CH4 and volatile fatty acids in a microbial electrosynthesis cell with a continuous CO2 supply. First, the impact of several transition metal ions (Ni2+, Fe2+, Cu2+, Sn2+, Mn2+, MoO42-, and Bi3+) on hydrogenotrophic and acetoclastic methanogenic microbial activity was evaluated in a series of batch bottle tests incubated with anaerobic sludge and a pre-defined concentration of dissolved transition metals. While Cu is considered a promising catalyst for the electrocatalytic conversion of CO2 to short chain fatty acids such as acetate, its presence as a Cu2+ ion was demonstrated to significantly inhibit the microbial production of CH4 and acetate. At the same time, CH4 production increased in the presence of Bi3+ (0.1 g L-1) and remained unchanged at the same concentration of Sn2+. Since Sn is of interest due to its catalytic properties in the electrochemical CO2 conversion, Bi and Sn were added to the cathode compartment of a laboratory-scale microbial electrosynthesis cell (MESC) to achieve an initial concentration of 0.1 g L-1. While an initial increase in CH4 (and acetate for Sn2+) production was observed after the first injection of the metal ions, after the second injection, CH4 production declined. Acetate accumulation was indicative of the reduced activity of acetoclastic methanogens, likely due to the high partial pressure of H2. The modification of a carbon-felt electrode by the electrodeposition of Sn metal on its surface prior to cathode inoculation with anaerobic sludge showed a doubling of CH4 production in the MESC and a lower concentration of acetate, while the electrodeposition of Bi resulted in a decreased CH4 production.

Microbial Fuel Cell Biosensor with Capillary Carbon Source Delivery for Real-Time Toxicity Detection.

A microbial fuel cell (MFC) biosensor with an anode as a sensing element is often unreliable at low or significantly fluctuating organic matter concentrations. To remove this limitation, this work demonstrates capillary action-aided carbon source delivery to an anode-sensing MFC biosensor for use in carbon-depleted environments, e.g., potable water. First, different carbon source delivery configurations using several thread types, silk, nylon, cotton, and polyester, are evaluated. Silk thread was determined to be the most suitable material for passive delivery of a 40 g L-1 acetate solution. This carbon source delivery system was then incorporated into the design of an MFC biosensor for real-time detection of toxicity spikes in tap water, providing an organic matter concentration of 56 ± 15 mg L-1. The biosensor was subsequently able to detect spikes of toxicants such as chlorine, formaldehyde, mercury, and cyanobacterial microcystins. The 16S sequencing results demonstrated the proliferation of Desulfatirhabdium (10.7% of the total population), Pelobacter (10.3%), and Geobacter (10.2%) genera. Overall, this work shows that the proposed approach can be used to achieve real-time toxicant detection by MFC biosensors in carbon-depleted environments.

Evaluation of biocathode materials for microbial electrosynthesis of methane and acetate.

This study compares carbon felt (CF), granular activated carbon (GAC), and a conductive acrylonitrile butadiene styrene (cABS) polymer cathodes for CH4 and acetate production in a microbial electrosynthesis (MES) cell. At an applied voltage of 2.8 V and continuous CO2 flow, the CF biocathode MES cell showed the highest CH4 production rate of 1420 ± 225 mL Vc-1 d-1 (Vc = cathode volume), also producing acetate at a rate of 710 ± 110 mg Vc-1 d-1. The volumetric rates of acetate and CH4 production decreased when using the GAC cathode (720 ± 94 mL Vc-1 d-1 and 236 ± 65 mg Vc-1 d-1, respectively). When the cABS cathode was used, the CH4 production declined to 250 ± 35 mL Vc-1 d-1, while the acetate production increased to 1105 ± 130 mg Vc-1 d-1. The biocatalytic activity of cABS increased after in-situ electrodeposition of Ni and Fe, resulting in a current increase from 205 mA to 380 mA accompanied by increasing acetate and ethanol production (1405 mg Vc-1 d-1 and 240 mg Vc-1 d-1, respectively), while the CH4 production decreased. The cABS cathode showed the highest specific (per surface area) activity for acetate and CH4 production.

A comparative analysis of biopolymer production by microbial and bioelectrochemical technologies.

Production of biopolymers from renewable carbon sources provides a path towards a circular economy. This review compares several existing and emerging approaches for polyhydroxyalkanoate (PHA) production from soluble organic and gaseous carbon sources and considers technologies based on pure and mixed microbial cultures. While bioplastics are most often produced from soluble sources of organic carbon, the use of carbon dioxide (CO2) as the carbon source for PHA production is emerging as a sustainable approach that combines CO2 sequestration with the production of a value-added product. Techno-economic analysis suggests that the emerging approach of CO2 conversion to carboxylic acids by microbial electrosynthesis followed by microbial PHA production could lead to a novel cost-efficient technology for production of green biopolymers.

On-line monitoring of water quality with a floating microbial fuel cell biosensor: field test results.

Real-time biomonitoring using microbial fuel cell (MFC) based biosensors have been demonstrated in several laboratory studies, but field validation is lacking. This study describes the long-term performance of an MFC based biosensor developed for real-time monitoring of changes in the water quality of a metal-contaminated stream. After a startup in the laboratory, biosensors were deployed in a stream close to an active mining complex in Sudbury, ON, Canada. Three sites within the stream were selected for biosensors installation based on their positions relative to the mining complex discharge points - upstream (lowest heavy metals concentration), midpoint and downstream. The biosensors installed at these sites were able to detect, in real-time, temporal changes in the water quality over a 2-month period. The biosensor response was confirmed by the results of a conventional toxicity assay (48-h acute Daphnia magna) as well as analytical measurements of heavy metals concentration in the stream. We conclude that the biosensor could detect changes in the overall water quality of the stream despite the uncontrolled situations typical for field operations as compared to laboratory conditions. To further explain the results observed during the field test, the rapid Microtox bioassay and D. magna assay were used to investigate the possible contributions of the two dominant mining metals (Nickel and Copper) to water toxicity in the test area.

Microbial fuel cell soft sensor for real-time toxicity detection and monitoring.

Real-time toxicity detection and monitoring using a microbial fuel cell (MFC) is often based on observing current or voltage changes. Other methods of obtaining more information on the internal state of the MFC, such as electrochemical impedance spectroscopy (EIS), are invasive, disruptive, time consuming, and may affect long-term MFC performance. This study proposes a soft sensor approach as a non-invasive real-time method for evaluating the internal state of an MFC biosensor during toxicity monitoring. The proposed soft sensor approach is based on estimating the equivalent circuit model (ECM) parameters in real time. A flow-through MFC biosensor was operated at several combinations of carbon source (acetate) and toxicant (copper) concentrations. The ECM parameters, such as internal resistance, capacitance, and open-circuit voltage, were estimated in real time using a numerical parameter estimation procedure. The soft sensor approach proved to be an adequate replacement for EIS measurements in quantifying changes in the biosensor internal parameters. The approach also provided additional information, which could lead to earlier detection of the toxicity onset.

Tellurium compound provides pro-apoptotic signaling in drug resistant multiple myeloma.

Multiple Myeloma, effectively treated by chemotherapeutic drugs, relapses due to drug resistance. We tested here the capacity of mesenchymal stromal cells, from the bone marrow of patients or from adipose tissue of healthy individuals, to induce drug resistance in Myeloma cell lines. We show that drug resistance can be achieved by factors secreted by the various MSC's. Mass spectrometry analysis of MSC's conditioned media revealed that fibronectin, was particularly instrumental in providing anti-apoptotic signals to MM cells. Moreover, we demonstrate that SAS ([octa-O-bis-(R,R)tartarate ditellurane]), an immunomodulator Tellurium compound, is not only able of blocking the physical interaction between MM cells and fibronectin but is also capable of re-sensitizing the cells to the chemotherapeutic drugs. Finally, we show that this re-sensitization is coupled with the blocking of pAKT induction, in MM cells, by the MSC's. These results indicate that SAS may be useful in the treatment of drug resistant MM.

Selenite and selenate removal in a permeable flow-through bioelectrochemical barrier.

This study demonstrated the removal of selenite and selenate in flow-through permeable bioelectrochemical barriers (microbial electrolysis cells, MECs). The bioelectrochemical barriers consisted of cathode and anode electrode compartments filled with granular carbon or metallurgical coke. A voltage of 1.4 V was applied to the electrodes to enable the bioelectrochemical removal of selenium species. For comparison, a similarly designed permeable anaerobic biobarrier filled with granular carbon was operated without voltage. All biobarrier setups were fed with water containing up to 5,000 µg L-1 of either selenite or selenate and 70 mg L-1 of acetate as a source of organic carbon. Significant removal of selenite and selenate was observed in MEC experimental setups, reaching 99.5-99.8% over the course of the experiment, while in the anaerobic biobarrier the removal efficiency did not exceed 88%. By simultaneously operating several setups and changing operating parameters (selenium species, influent Se and acetate concentrations, etc.) we demonstrated enhanced removal of Se species under bioelectrochemical conditions.

Treatment of Multiple Myeloma Using Chimeric Antigen Receptor T Cells with Dual Specificity.

Chimeric antigen receptor (CAR) T-cell therapy has shown remarkable successes in fighting B-cell leukemias/lymphomas. Promising response rates are reported in patients treated with B-cell maturation antigen (BCMA) CAR T cells for multiple myeloma. However, responses appear to be nondurable, highlighting the need to expand the repertoire of multiple myeloma-specific targets for immunotherapy and to generate new CAR T cells. Here, we developed a "dual-CAR" targeting two multiple myeloma-associated antigens and explored its safety and efficacy. To reduce the "off-target" toxicity, we used the recognition of paired antigens that were coexpressed by the tumor to induce efficient CAR T-cell activation. The dual-CAR construct presented here was carefully designed to target the multiple myeloma-associated antigens, taking into consideration the distribution of both antigens on normal human tissues. Our results showed that the CD138/CD38-targeted dual CAR (dCAR138-38) elicited a potent anti-multiple myeloma response both in vitro and in vivo NSG mice transplanted with a multiple myeloma cell line and treated with dCAR138-38 showed median survival of 97 days compared with 31 days in the control group treated with mock-lymphocytes. The dCAR138-38 showed increased specificity toward cells expressing both targeted antigens compared with single-antigen-expressing cells and low activity toward primary cells from healthy tissues. Our findings indicated that the dCAR138-38 may provide a potent and safe alternative therapy for patients with multiple myeloma.

Online monitoring of heavy metal-related toxicity using flow-through and floating microbial fuel cell biosensors.

Elevated concentrations of heavy metals in water caused by mining activities create significant risks to the environment. Traditional biological methods used to assess heavy metal-related toxicity in aquatic environments are lengthy and labor intensive. Real-time biomonitoring approaches eliminate some of these limitations and provide a more accurate indication of toxicity. This study describes the performance of a flow-through and floating design microbial fuel cell (MFC) biosensors for real-time detection of copper (Cu) and other heavy metal-related toxicity in aquatic environments. Several biomonitoring tests were carried out using Cu and mining effluents as toxicants. The biosensors were able to detect, in real-time, Cu-related toxicity at concentrations as low as 35 - 40 µg L-1, as confirmed by a Daphnia assay. A comparison of the floating biosensor's outputs with Daphnia magna survival rates showed a linear correlation with a coefficient of determination (R2) higher than 0.9. In addition, the flow-through biosensor was shown to be able to detect  differences in the quality of two mining effluents with different compositions of heavy metals. Finally, the biosensor's real-time field performance was investigated in two aquatic environments in the Sudbury, Ontario region of Canada.

Harvesting Energy from Multiple Microbial Fuel Cells with a High-Conversion Efficiency Power Management System.

Direct electricity production from waste biomass in a microbial fuel cell (MFC) offers the advantage of producing renewable electricity at a high Coulombic efficiency. However, low MFC voltage (below 0.5 V) necessitates the simultaneous operation of multiple MFCs controlled by a power management system (PMS) adapted for operating bioelectrochemical systems with complex nonlinear dynamics. This work describes a novel PMS designed for efficient energy harvesting from multiple MFCs. The PMS includes a switched-capacitor-based converter, which ensures operation of each MFC at its maximum power point (MPP) by regulating the output voltage around half of its open-circuit voltage. The open-circuit voltage of each MFC is estimated online regardless of MFC internal parameter knowledge. The switched-capacitor-based converter is followed by an upconverter, which increases the output voltage to a required level. Advantages of the proposed PMS include online MPP tracking for each MFC and high (up to 85%) power conversion efficiency. Also, the PMS prevents voltage reversal by disconnecting an MFC from the circuit whenever its voltage drops below a predefined threshold. The effectiveness of the proposed PMS is verified through simulations and experimental runs.

On-line monitoring of heavy metals-related toxicity with a microbial fuel cell biosensor.

This study describes an environmental biosensor for real time toxicity monitoring, which exploits high sensitivity of a microbial fuel cell (MFC) to variations in concentrations of electron donors and acceptors. Fast biosensor response to changes in total heavy metal concentration of a mining rock drainage was observed in laboratory tests with acceptable repeatability and a coefficient of determination (R2) of 0.95-0.97. The biosensor response is attributed to interference of heavy metals with the activity of electroactive microorganisms. Biomolecular analysis of the anodic electroactive biofilms showed significant population differences between microbial populations of the biosensor exposed to heavy metals and a non-exposed (control) biosensor. Furthermore, the biosensor outputs were highly correlated (R2 = 0.92) with the results of the Microtox toxicity assay. The results of this study contribute towards the development of a simple MFC-based biosensor capable of detecting, in real-time, changes in environmental conditions and providing a tool for on-site toxicity monitoring.

Impaired lymphocyte reconstitution after autologous transplant is associated with apoptosis of CD8+ T cells and adverse clinical outcome.

We noticed that the lymphocyte counts, after autologous hematopoietic stem cell transplantation, oscillated during the first 4 post-transplant months. Thereafter, the lymphocyte counts stabilized and segregated the patients into two groups, those who normalized their lymphocyte counts and those with prolonged lymphopenia. In both groups, the CD4 counts remained low for at least 6 months. However, in approximately half of the patient, the CD8 counts increased to normal or above normal values. Patients with prolonged lymphopenia had higher rates of lymphocytes' spontaneous apoptosis and the lymphocytes in patients who restored their counts expressed the intracellular CD14-derived MO2 epitope that protects the cells from apoptosis. These findings were translated to longer disease-free survival and overall survival in patients who restored the CD8 counts. Collectively, our data show that post-transplant lymphocytes that express intracellular CD14-MO2 epitope have survival advantage.

Fluorescence-based real time monitoring and diagnostics of recombinant Pichia pastoris cultivations in a bioreactor.

This study describes the application of the multivariate curve resolution (MCR) analysis technique for real-time analysis of culture fluorescence during recombinant Pichia pastoris cultivation in a bioreactor. Fluorescence spectra were acquired with an on-line dual excitation wavelength fluorometer and then used to develop a real time MCR-based bioprocess monitoring and diagnostics tool. Initial bioreactor experiments using two similar recombinant antibody secreting P. pastoris cell lines showed significant differences in protein production. To distinguish between the contributions of operating conditions and the specific cell line's genetic composition to the observed differences in protein production, the bioreactor experiments were repeated and accompanied by real time MCR analysis. The tests demonstrated high sensitivity of MCR-derived "pure concentration" profiles to growth as well as to initial conditions, thus enabling real-time cultivation process trend diagnostics and fault detection. © 2018 Her Majesty the Queen in Right of Canada © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 35: e2761, 2019.

A comparison of microbial fuel cell and microbial electrolysis cell biosensors for real-time environmental monitoring.

This study compares the biosensing performance of a microbial fuel cell (MFC) and a microbial electrolysis cell (MEC). Initial tests provided a qualitative comparison of MFC and MEC currents after the anode compartment liquid (anolyte) was spiked with acetate, or sulphates of NH4+, Na+, Mg2+, Fe2+, or a fertilizer solution. Current measurements showed that the MFC sensor had a faster response time, higher sensitivity, and faster recovery time after the spike. Following the spike tests, the MFC and MEC were operated in a continuous flow mode at several influent concentrations of acetate, and sulphates of NH4+, Na+, and Fe2+. The continuous flow tests confirmed the better performance of the MFC sensor, which was selected for further experiments. Two MFC sensors were used for real-time (on-line) COD measurements of brewery wastewater. Regression analysis showed a strong correlation between the MFC power output and COD concentrations in the anode compartment with a coefficient of determination (R2) of 0.97. Overall, results of this study suggest that an MFC-based sensor can be successfully used as a simple and cost-efficient real-time monitoring tool.

Dynamic model of a municipal wastewater stabilization pond in the arctic.

Waste stabilisation ponds (WSPs) are the method of choice for sewage treatment in most arctic communities because they can operate in extreme climate conditions, require a relatively modest investment, are passive and therefore easy and inexpensive to operate and maintain. However, most arctic WSPs are currently limited in their ability to remove carbonaceous biochemical oxygen demand (CBOD), total suspended solids (TSS) and ammonia-nitrogen. An arctic WSP differs from a 'southern' WSP in the way it is operated and in the conditions under which it operates. Consequently, existing WSP models cannot be used to gain better understanding of the arctic lagoon performance. This work describes an Arctic-specific WSP model. It accounts for both aerobic and anaerobic degradation pathways of organic materials and considers the periodic nature of WSP operation as well as the partial or complete freeze of the water in the WSP during winter. A uniform, multi-layer (ice, aerobic, anaerobic and sludge) approach was taken in the model development, which simplified and expedited numerical solution of the model, enabling efficient model calibration to available field data.

Bioelectrochemical anaerobic sewage treatment technology for Arctic communities.

This study describes a novel wastewater treatment technology suitable for small remote northern communities. The technology is based on an enhanced biodegradation of organic carbon through a combination of anaerobic methanogenic and microbial electrochemical (bioelectrochemical) degradation processes leading to biomethane production. The microbial electrochemical degradation is achieved in a membraneless flow-through bioanode-biocathode setup operating at an applied voltage below the water electrolysis threshold. Laboratory wastewater treatment tests conducted through a broad range of mesophilic and psychrophilic temperatures (5-23 °C) using synthetic wastewater showed a biochemical oxygen demand (BOD5) removal efficiency of 90-97% and an effluent BOD5 concentration as low as 7 mg L-1. An electricity consumption of 0.6 kWh kg-1 of chemical oxygen demand (COD) removed was observed. Low energy consumption coupled with enhanced methane production led to a net positive energy balance in the bioelectrochemical treatment system.

Removal of organic carbon and nitrogen in a membraneless flow-through microbial electrolysis cell.

This study evaluated performance of an upflow membraneless microbial electrolysis cell (MEC) with flow-through electrodes for wastewater treatment. First, methane production and COD removal were evaluated in continuous flow experiments carried out using synthetic and municipal wastewater. A 29-75% increase in methane production was observed under bioelectrochemical conditions as compared to an anaerobic control. Next, simultaneous removal of COD and nitrogen was studied under microaerobic conditions created by continuous air injection to the anodic compartment of the MEC. While the presence of oxygen decreased Coulombic efficiency due to aerobic degradation of COD, enhanced ammonium removal with near zero nitrite and nitrate effluent concentrations was observed. Evidence of direct ammonium oxidation at the anode as well as nitrite and nitrate reduction at the cathode was obtained by comparing performances of MECs operated under anaerobic and microaerobic conditions with the control reactor operated at zero applied voltage.

Maximizing the productivity of the microalgae Scenedesmus AMDD cultivated in a continuous photobioreactor using an online flow rate control.

In this study, production of the microalga Scenedesmus AMDD in a 300 L continuous flow photobioreactor was maximized using an online flow (dilution rate) control algorithm. To enable online control, biomass concentration was estimated in real time by measuring chlorophyll-related culture fluorescence. A simple microalgae growth model was developed and used to solve the optimization problem aimed at maximizing the photobioreactor productivity. When optimally controlled, Scenedesmus AMDD culture demonstrated an average volumetric biomass productivity of 0.11 g L-1 d-1 over a 25 day cultivation period, equivalent to a 70 % performance improvement compared to the same photobioreactor operated as a turbidostat. The proposed approach for optimizing photobioreactor flow can be adapted to a broad range of microalgae cultivation systems.

A comparison of simultaneous organic carbon and nitrogen removal in microbial fuel cells and microbial electrolysis cells.

This study demonstrates simultaneous carbon and nitrogen removal in laboratory-scale continuous flow microbial fuel cell (MFC) and microbial electrolysis cell (MEC) and provides side-by side comparison of these bioelectrochemical systems. The maximum organic carbon removal rates in MFC and MEC tests were similar at 5.1 g L(-1) d(-1) and 4.16 g L(-1) d(-1), respectively, with a near 100% carbon removal efficiency at an organic load of 3.3 g L(-1) d(-1). An ammonium removal efficiency of 30-55% with near-zero nitrite and nitrate concentrations was observed in the MFC operated at an optimal external resistance, while open-circuit MFC operation resulted in a reduced carbon and ammonium removal of 53% and 21%, respectively. In the MEC ammonium removal was limited to 7-12% under anaerobic conditions, while micro-aerobic conditions increased the removal efficiency to 31%. Also, at zero applied voltage both carbon and ammonium removal efficiencies were reduced to 42% and 4%, respectively. Based on the observed performance under different operating conditions, it was concluded that simultaneous carbon and nitrogen removal was facilitated by concurrent anaerobic and aerobic biotransformation pathways at the anode and cathode, which balanced bioelectrochemical nitrification and denitrification reactions.