A bipolar membrane combined with ferric iron reduction as an efficient cathode system in microbial fuel cells

There is a need for alternative catalysts for oxygen reduction in the cathodic compartment of a microbial fuel cell (MFC). In this study, we show that a bipolar membrane combined with ferric iron reduction on a graphite electrode is an efficient cathode system in MFCs. A flat plate MFC with graphite felt electrodes, a volume of 1.2 L and a projected surface area of 290 cm2 was operated in continuous mode. Ferric iron was reduced to ferrous iron in the cathodic compartment according to Fe(3+) + e(-) --> Fe2+ (E0 = +0.77 V vs NHE, normal hydrogen electrode). This reversible electron transfer reaction considerably reduced the cathode overpotential. The low catholyte pH required to keep ferric iron soluble was maintained by using a bipolar membrane instead of the commonly used cation exchange membrane. For the MFC with cathodic ferric iron reduction, the maximum power density was 0.86 W/m2 at a current density of 4.5 A/m2. The Coulombic efficiency and energy recovery were 80-95% and 18-29% respectively.     

Discovery of Selective Luteinizing Hormone Receptor Agonists Using the Bivalent Ligand Method

Two series of dimeric ligands for a G‐protein‐coupled receptor were prepared that differ by the interconnecting spacer system. Biological evaluation revealed that both dimeric series exhibit unique biological properties relative to their monomeric counterparts.

     

Rapid Internalization and Nuclear Translocation of CCL5 and CXCL4 in Endothelial Cells

The chemokines CCL5 and CXCL4 are deposited by platelets onto endothelial cells, inducing monocyte arrest. Here, the fate of CCL5 and CXCL4 after endothelial deposition was investigated. Human umbilical vein endothelial cells (HUVECs) and EA.hy926 cells were incubated with CCL5 or CXCL4 for up to 120 min, and chemokine uptake was analyzed by microscopy and by ELISA. Intracellular calcium signaling was visualized upon chemokine treatment, and monocyte arrest was evaluated under laminar flow. Whereas CXCL4 remained partly on the cell surface, all of the CCL5 was internalized into endothelial cells. Endocytosis of CCL5 and CXCL4 was shown as a rapid and active process that primarily depended on dynamin, clathrin, and G protein-coupled receptors (GPCRs), but not on surface proteoglycans. Intracellular calcium signals were increased after chemokine treatment. Confocal microscopy and ELISA measurements in cell organelle fractions indicated that both chemokines accumulated in the nucleus. Internalization did not affect leukocyte arrest, as pretreatment of chemokines and subsequent washing did not alter monocyte adhesion to endothelial cells. Endothelial cells rapidly and actively internalize CCL5 and CXCL4 by clathrin and dynamin-dependent endocytosis, where the chemokines appear to be directed to the nucleus. These findings expand our knowledge of how chemokines attract leukocytes to sites of inflammation.     

Multivalent Antibody-Recruiting Macromolecules: Linking Increased Binding Affinity with Enhanced Innate Immune Killing

Antibody-recruiting molecules (ARMs) are a novel class of immunotherapeutics. They are capable of introducing antibodies onto disease-relevant targets such as cancer cells, bacterial cells or viruses. This can induce antibody-mediated immune responses such as antibody-dependent cellular cytotoxicity (ADCC), complement-dependent cytotoxicity (CDC) and antibody-dependent phagocytosis (ADCP), which can kill the pathogen. In contrast to the classic ARMs, multivalent ARMs could offer the advantage of increasing the efficiency of antibody recruitment and subsequent innate immune killing. Such compounds consist of multiple target-binding termini (TBT) and/or antibody-binding termini (ABT). Those multivalent interactions are able to convert low binding affinities into increased binding avidities. This minireview summarizes the current status of multivalent ARMs and gives insight into possible benefits, hurdles still to be overcome and future perspectives.     

Steady-state performance and chemical efficiency of Microbial Electrolysis Cells

The objective of this paper was to study MEC performance at steady-state conditions in continuous mode and to analyse MEC performance in terms of chemical efficiency. At steady-state operation, a current density of 10.2 A m⁻² (applied voltage 1.0 V) for a set-up with an AEM was produced, compared to 7.2 A m⁻² for a set-up with a CEM. For all applied voltages, total internal resistance for the AEM configuration was lower than or the CEM configuration. Therefore, energy input for the AEM configuration is lower than for the CEM configuration. In case a CEM is used, the conductivity in the cathode reaches high values: >130 mS cm⁻¹. This conductivity is mainly caused by the presence of Na⁺ (7.8 g L⁻¹), K⁺ (12.2 g L⁻¹) and OH⁻ (8.3 g L⁻¹). Furthermore, MECs perform better at high buffer and electrolyte concentrations. However, as current density does not increase proportionally with increase in chemicals, the effectiveness of chemical addition decreases when more chemicals are added. Therefore, addition of chemicals and buffer does not necessarily enhance performance but increases operational costs.     

Performance of a scaled-up Microbial Fuel Cell with iron reduction as the cathode reaction

Scale-up studies of Microbial Fuel Cells are required before practical application comes into sight. We studied an MFC with a surface area of 0.5 m² and a volume of 5 L. Ferric iron (Fe³⁺) was used as the electron acceptor to improve cathode performance. MFC performance increased in time as a combined result of microbial growth at the bio-anode, increase in iron concentration from 1 g L⁻¹ to 6 g L⁻¹, and increased activity of the iron oxidizers to regenerate ferric iron. Finally, a power density of 2.0 W m⁻² (200 W m⁻³) was obtained. Analysis of internal resistances showed that anode resistance decreased from 109 to 7 mΩ m², while cathode resistance decreased from 939 to 85 mΩ m². The cathode was the main limiting factor, contributing to 58% of the total internal resistance. Maximum energy efficiency of the MFC was 41%.     

The Promises of Natural Killer Cell Therapy in Endometriosis

Endometriosis is a gynaecological disease defined by the growth of endometrium-like tissue outside the uterus. The disease is present in approximately 5–10% of women of reproductive age and causes pelvic pain and infertility. The pathophysiology is not completely understood, but retrograde menstruation and deficiency in natural killer (NK) cells that clear endometriotic cells in the peritoneal cavity play an important role. Nowadays, hormonal therapy and surgery to remove endometriosis lesions are used as treatment. However, these therapies do not work for all patients, and hormonal therapy prevents patients from getting pregnant. Therefore, new treatment strategies should be developed. Since the cytotoxicity of NK cells is decreased in endometriosis, we performed a literature search into the possibility of NK cell therapy. Available treatment options include the inhibition of receptor–ligand interaction for KIR2DL1, NKG2A, LILRB1/2, and PD-1/PD-L1; inhibition of TGF-β; stimulation of NK cells with IL-2; and mycobacterial treatment with BCG. In preclinical work, these therapies show promising results but unfortunately have side effects, which have not specifically been studied in endometriosis patients. Before NK cell treatment can be used in the clinic, more research is needed.     

Gas diffusion electrodes improve hydrogen gas mass transfer for a hydrogen oxidizing bioanode

Background

Bioelectrochemical systems (BESs) are capable of recovery of metals at a cathode through oxidation of organic substrate at an anode. Recently, also hydrogen gas was used as an electron donor for recovery of copper in BESs. Oxidation of hydrogen gas produced a current density of 0.8 A m^‐2 and combined with Cu²⁺ reduction at the cathode, produced 0.25 W m^‐2. The main factor limiting current production was the mass transfer of hydrogen to the biofilm due to the low solubility of hydrogen in the anolyte. Here, the mass transfer of hydrogen gas to the bioanode was improved by use of a gas diffusion electrode (GDE).

Results

With the GDE, hydrogen was oxidized to produce a current density of 2.9 A m^‐2 at an anode potential of –0.2 V. Addition of bicarbonate to the influent led to production of acetate, in addition to current. At a bicarbonate concentration of 50 mmol L^‐1, current density increased to 10.7 A m^‐2 at an anode potential of –0.2 V. This increase in current density could be due to oxidation of formed acetate in addition to oxidation of hydrogen, or enhanced growth of hydrogen oxidizing bacteria due to the availability of acetate as carbon source. The effect of mass transfer was further assessed through enhanced mixing and in combination with the addition of bicarbonate (50 mmol L^‐1) current density increased further to 17.1 A m^‐2.

Conclusion

Hydrogen gas may offer opportunities as electron donor for bioanodes, with acetate as potential intermediate, at locations where excess hydrogen and no organics are available. © 2017 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.