Cell-envelope proteinases from lactic acid bacteria: Biochemical features and biotechnological applications

Proteins displayed on the cell surface of lactic acid bacteria (LAB) perform diverse and important biochemical roles. Among these, the cell-envelope proteinases (CEPs) are one of the most widely studied and most exploited for biotechnological applications. CEPs are important players in the proteolytic system of LAB, because they are required by LAB to degrade proteins in the growth media into peptides and/or amino acids required for the nitrogen nutrition of LAB. The most important area of application of CEPs is therefore in protein hydrolysis, especially in dairy products. Also, the physical location of CEPs (i.e., being cell-envelope anchored) allows for relatively easy downstream processing (e.g., extraction) of CEPs. This review describes the biochemical features and organization of CEPs and how this fits them for the purpose of protein hydrolysis. It begins with a focus on the genetic organization and expression of CEPs. The catalytic behavior and cleavage specificities of CEPs from various LAB are also discussed. Following this, the extraction and purification of most CEPs reported to date is described. The industrial applications of CEPs in food technology, health promotion, as well as in the growing area of water purification are discussed. Techniques for improving the production and catalytic efficiency of CEPs are also given an important place in this review.     

Bimetallic PtPd nanoparticles relying on CoNiO2 and reduced graphene oxide as a most operative electrocatalyst toward ethanol fuel oxidation

Of late, fuel cells have drawn great attentions owing to high-energy demands, fossil fuel depletion and worldwide environmental pollution. Direct ethanol fuel cell (DEFC) constituted as one of the most promising sources of green energy, howbeit the ethanol oxidation reaction (EOR) sluggish kinetic is one of the essential challenges toward the commercialization of DEFCs. Herein, we introduce bimetallic catalyst on CoNiO₂ modified reduced graphene oxide (rGO) to completely exploit the advantages of nano-surface structures as well as the reduction of Pt and Pd loading in fuel cells. With the combined advantages of PtPd, CoNiO₂ and rGO, a significant enhancement in electrocatalytic behavior, stability and CO poisoning tolerance of PtPd have been observed. Regarding the implications, PtPd/CoNiO₂/rGO is greatly preferable than Pt/CoNiO₂/rGO and Pd/CoNiO₂/rGO in terms of high electroactive surface area (ECSA), electro-catalytic activity, and lower onset potential (E_ons) towards the EtOH oxidation in alkaline media. Furthermore, the chronoamperometry curve (CA) illustrated 77% after 3600 s which is dramatically soared compared with the other electrodes (≤40%), demonstrating the high stability of the PtPd bimetallic nanoparticle electrocatalyst. Ultimately, PtPd/CoNiO₂/rGO nanocomposite is found to be an excellent anode electrocatalyst for application in DEFCs.     

Growth of Ni/Mo/Cu on carbon fiber paper: An efficient electrocatalyst for hydrogen evolution reaction

The exploration of efficient catalysts toward hydrogen evolution reaction (HER) is still an urgent task. In this paper, Ni/Mo/Cu/C and Ni/Mo/C electrode were obtained by conventional pulse voltammetry, which acted as cathode in microbial electrolysis cells (MECs). The prepared samples are analyzed using SEM, XRD, XPS and electrochemical analysis techniques. Results indicated that the Ni/Mo/Cu coating has a rough and globular structure and presents high current density, a lower Tafel slope of 23.9 mV/dec than 30 mV/dec of Pt, which exceeds the electrochemical activity of Pt electrode. Its remarkably enhanced electrocatalytic activity is attributed to the high surface area, high conductivity as well as synergistic interaction among Ni, Mo and Cu.     

Recent advances in two-dimensional Pt based electrocatalysts for methanol oxidation reaction

Direct methanol fuel cells (DMFCs) had been attracted considerable attention for its advantages of high energy density, simplified systems and readily transportation and storage of methanol. However, the notoriously sluggish kinetics of methanol oxidation reaction (MOR) of the anode reaction, had greatly affected the commercialization of DMFCs. On one hand, Pt based catalyst are still the most effective MOR catalysts, while the high cost caused by the high loadings of electrocatalyst to compensate the low MOR activity impedes the wide accessible of DMFCs. In addition, the occurrence of catalyst poisoning owing to the strong interaction between Pt and carbon monoxide (CO) generated during the MOR processing, further leading to the fast decay in the performance and stability of MOR electrocatalysts. Two-dimensional (2D) Pt based nanostructures is regarded to be one promising and effective class of MOR electrocatalysts, and attracted much attention due to the high electron mobility, highly exposed active sites, and extraordinary thermal conduction. In this review, the mechanism of MOR was firstly introduced, and then the synthesis conditions, structure characteristics and methanol oxidation performances both in acidic and alkaline dielectric of 2D Pt based nanocatalysts were introduced. Subsequently, we briefly analyzed the structural characteristics of 2D Pt based nanocatalysts and their advantages, including the low platinum loadings, high specific surface area and majority of atomic active sites exposed. Finally, the opportunities and challenges for designing of advanced 2D Pt based nanocatalysts was proposed and discussed.     

Development and performance assessment of new solar and fuel cell-powered oxygen generators and ventilators for COVID-19 patients

In this study, a new solar-based fuel cell-powered oxygenation and ventilation system is presented for COVID-19 patients. Solar energy is utilized to operate the developed system through photovoltaic panels. The method of water splitting is utilized to generate the required oxygen through the operation of a proton exchange membrane water electrolyser. Moreover, the hydrogen produced during water splitting is utilized as fuel to operate the fuel cell system during low solar availability or the absence of solar irradiation. Transient simulations and thermodynamic analyses of the developed system are performed by accounting for the changes in solar radiation intensities during the year. The daily oxygen generation is found to vary between 170.4 kg/day and 614.2 kg/day during the year. Furthermore, the amount of daily hydrogen production varies between 21.3 kg/day and 76.8 kg/day. The peak oxygen generation rate attains a value of 18.6 g/s. Moreover, the water electrolysis subsystem entails daily exergy destruction in the range of 139.9–529.7 kWh. The maximum efficiencies of the developed system are found to be 14.3% energetically and 13.4% exergetically.     

Single-step inkjet-printed paper-origami arrayed air-breathing microfluidic microbial fuel cell and its validation

Microfluidic paper based microbial fuel cells (μP-MFCs) have gained considerable popularity due to their compact, quick and low-cost fluid manipulation paradigm. Compared to conventional technologies, paper as a substrate with advanced nanomaterial electrode material has many distinct advantages from point-of-care monitoring to energy harvesting. As a result, these have been used and are more popular in a variety of fields, such as health diagnostics, environmental and food quality management. By this encouragement, herein a portable microbial fuel cell as an origami array has been demonstrated using custom carbon electrodes with a modified the transition metal oxide MnO₂ nanomaterial. This customized electrode design was first printed using a tabletop PCB inkjet printer where the anode was further modified with synthesized MnO₂ nanoparticles. The entire cell was formed by folding the paper along predefined edges where the fuel, Shewanella putrefaciens, was streamed continuously via inherent capillary cation. Various studies, such as morphological, surface catalyst coating, amount loading and volumetric culture optimization experiments, have also been accomplished to find the most appropriate optimum parameter to enhance power conversion efficiency. The developed origami arrayed microbial fuel generated an open-circuit potential (OCP) for two parallel connected MFCs of 0.534 V and a maximum power density of 15.9 μW/cm² with a maximum current density of 130 μA/cm². In the end, the harvested power was used by powering the digital watch circuit through the ultra-low DC-DC booster board. Such an MFC origami array, with simple electrode manufacturing and modification process, has a great potential and bright future in Internet of Things (IoT) applications by making multiple stacks where the data can be monitored.     

Investigation of surficial and interfacial properties of BaCo0.4Fe0.4Zr0.1Y0.1O3-δ cathode directly on yttria-stabilized zirconia electrolyte for solid oxide fuel cell

The cobalt/iron-containing perovskites are the most promising cathodes for the intermediate-temperature solid oxide fuel cell (IT-SOFC). However, these cathodes are generally not directly applied on the currently available commercial yttria-stabilized zirconia (YSZ) electrolyte due to the issues of over-firing, harmful reaction and thermal incompatibility. BaCo_0.4Fe_0.4Zr_0.1Y_0.1O_3-δ (BCFZY) which contains both zirconium and yttrium ions can theoretically be more compatible with the YSZ electrolyte. This paper focuses on the surficial and interfacial properties of BCFZY directly prepared with YSZ under different conditions. The surface of BCFZY by the glycine-nitrate process (GNP) can form the nanoparticles in contrast to that by solid-state reaction (SSR). The peak power density of the cell with BCFZY-GNP cathode directly on YSZ electrolyte can reach 1250 mW cm⁻² at 750 °C, which is hardly achieved on the reported traditional cobalt/iron-containing cathodes. It is proved that BCFZY-GNP cathode fired at 900 °C can show more distinct nanoparticles with extensive specific surface area and better BCFZY|YSZ interface, which can promote both oxygen exchange and ion incorporation processes.     

Remaining useful life prediction of PEMFC based on cycle reservoir with jump model

Accurate prognosis of limited durability is one of the key factors for the commercialization of proton exchange membrane fuel cell (PEMFC) on a large scale. Thanks to ignoring the structure of the PEMFC and simplifying the prognostic process, the data-driven prognostic approaches was the commonly used for predicting remaining useful life (RUL) at present. In this paper, the proposed cycle reservoir with jump (CRJ) model improves the ESN model, changes the connection mode of neurons in the reservoir and speeds up the linear fitting process. The experiment will verify the performance of CRJ model to predict stacks voltage under static current and quasi-dynamic current conditions. In addition, the reliability of the CRJ model is verified with different amount of data as the training and test sets. The experimental results demonstrate that the CRJ model can achieve better effect in the remaining useful life prognosis of fuel cells.     

Validating the efficiency of γ-Al2O3/La0.6Sr0.4Co0.2Fe0.8O3-δ double-layer electrolyte for low temperature solid oxide fuel cell

Perovskite La_0.6Sr_0.4Co_0.2Fe_0.8O_3+δ (LSCF) as a promising cathode material possessed overwhelming electronic conduction along with certain ionic conductivity. Its strong electron conduction capability hinder the application of pure-phase LSCF as electrolyte in semiconductor membrane fuel cell (SMFC). In order to constrain the electron transport and take advantage of the decent ion conduction of LSCF, a thin layer of γ-Al₂O₃ with insulating property was added as an electron barrier layer and combine with LSCF to form a two-layer structure electrolyte. Through adjusting the weight ratio of LSCF/γ-Al₂O₃ to optimize the thickness of double layers, an open circuit voltage of 0.98 V and a maximum power density of 690 mW/cm² was received at 550 °C. At the same time, SEM, EIS and other characterization technology had proven that the LSCF/γ-Al₂O₃ bi-layer electrolyte can work efficiently at low temperature. The advantage of this work is the application of double-layer (γ-Al₂O₃/LSCF) structure electrolyte to instead of mixed material electrolyte in low-temperature solid oxide fuel cells. Structural innovation and the using of insulating materials provided clues for the further development of SMFC.