A Universal Chemical Method for Rational Design of Protein-Based Nanoreactors**

Self-assembly of a monomeric protease to form a multi-subunit protein complex “proteasome” enables targeted protein degradation in living cells. Naturally occurring proteasomes serve as an inspiration and blueprint for the design of artificial protein-based nanoreactors. Here we disclose a general chemical strategy for the design of proteasome-like nanoreactors. Micelle-assisted protein labeling (MAPLab) technology along with the N-terminal bioconjugation strategy is utilized for the synthesis of a well-defined monodisperse self-assembling semi-synthetic protease. The designed protein is programmed to self-assemble into a proteasome-like nanostructure which preserves the functional properties of native protease.     

Cross flow on transient double‐diffusive natural convection in inclined porous trapezoidal enclosures

This paper investigates the cross‐diffusion effects subject to exponential variable boundary conditions on transient double‐diffusive natural convection flow in an enclosure. The flow domain is a two‐dimensional inclined trapezoidal cavity filled with a porous medium. The top wall is assumed to be insulated and permeable, while the enclosure's bottom wall is subject to exponential varying temperature and concentration. The prescribed temperature and concentration are different at the vertical walls. Conservation equations are used as the governing equations. The finite element Galerkin weighted residual method, in association with the Newton‐Raphson scheme is employed to solve the system of coupled nondimensional equations. The numerical tests are confirmed with existing literature and are found to be in excellent agreement. The simulations results for stream functions, isotherms, and isoconcentrations are discussed for the various flow parameters. A sensitivity analysis using the response surface method suggests that the average Nusselt and Sherwood numbers are more sensitive to the cross‐diffusion effects. It is further observed that the cross‐diffusion terms stabilize the sensitivity to the angle of inclination.     

On the development of uniaxially‐oriented PET tapes for weaving,woven tape fabrics,and their applications

This article reports the development of weavable, uniaxially‐oriented PET tape, and woven‐tape fabric. Fabric from uniaxially‐oriented polypropylene (PP) tape has been commercially produced since the 1960s, and it is the dominant material for flexible industrial packaging, carpet backing, geotextiles and self‐reinforced composites. Attempts had been made over the same period to produce similar poly(ethylene terephthalate) (PET) tape fabric, knowing that it would offer superior performance over PP due to PET's higher stiffness and strength, lower creep, abrasion resistance, and higher temperature capability. However, these attempts could not be translated into industrial production because the PET tapes had a tendency to splinter when subjected to sudden pulls and twists in the weaving loom. This was solved here by blending polymeric additives such as 2% polycarbonate (PC) and 2% linear low‐density polyethylene (LLDPE). Transmission electron microscopy of the oriented tapes showed the 2% PC formed a profusion of nano ellipsoids that adhered well to the PET matrix, and these prevented axial cracks from running through in a brittle manner. The LLDPE formed larger domains with poorer adhesion, but it imparted resistance to splitting from twists and axial folding. The combination of PC and polyolefin imparted a synergistic toughening of the tape. POLYM. ENG. SCI., 59:E120–E132, 2019. © 2018 Society of Plastics Engineers     

Catalyst design for maximizing C5+ yields during Fischer-Tropsch synthesis

Fischer-Tropsch (FT) process has great potential to accomplish energy security but also for utilizing greenhouse gases to address the energy problem. Different kinds of feedstocks like coal, biomass (via gasification), CO₂, methane (via reforming), and nonconventional energy sources are used to obtain the syn-gas (CO and H₂). The formation of hydrocarbons in the FT process follows ASF distribution over the majority of the catalysts. It can be overcome by the application of a suitable catalyst, controlling the active metal interaction with the support and interaction of formed hydrocarbon with the support. The ratio of syn-gas is important to maintain the desired conversion and to have more selectivity towards C₅+ products. Increase in the H₂: CO ratios in the feed increases C₅+ products and methane decreases. Whereas with the decrease in the ratios increases undesirable reactions and methane formation. In this article, we have discussed the recent literature from the viewpoint of increasing the C₅+ selectivity. Support has a profound influence on product distribution. With the application of suitable support and controlling the interaction of the active sites yields the good CO conversion with fewer lighters and higher C₅+ hydrocarbons.     

Inclusion of low cost activated carbon for improving hydrogen production performance of TiO2 nanoparticles under natural solar light irradiation

Photocatalytic studies are primarily focused on the low cost and sustainable materials with suitable bandgap and high surface area. The ultra-fast electron-hole pair recombination and limited light absorptions affect the efficiency of photocatalyst in an adverse manner, which can be unravelled by choosing an efficient combination of photocatalysts and suitable co-catalyst/support materials. The present work explores the combination of low-cost and high potential activated carbon and TiO₂ as a nanocomposite, prepared through a one-pot hydrothermal process for hydrogen production under natural solar light irradiation. Among the synthesized photocatalysts, the one calcined at 400 °C for 2 h was found to be the best catalyst, which exhibited 3.5 times higher hydrogen production rate than the pristine TiO₂ while tested with water containing 5 vol.% glycerol. Importantly, the optimized nanocomposite was also tested for hydrogen production from simulated seawater under same conditions and it showed a hydrogen production rate of 20,383 μmol g^?1 h^?1, which is 2.4 times higher than the glycerol water solution. The enhanced hydrogen production rate is due to the reduced bandgap of AC-TiO₂ nanocomposite which offered more light absorption in the visible region compared to the pristine TiO₂. The XRD, Raman spectroscopy, TEM, and PL analysis were also examined to investigate the crystallinity, purity, morphology, and charge carrier recombination life time of the synthesized catalysts.     

Effect of reaction time and PVP contents on morphologies of hierarchical 3D flower-like ZnCo2O4 microstructures for energy storage devices

Hierarchical 3D flower-like ZnCo₂O₄ (ZCO) microstructures assembled from petal-like nanosheets/flakes of non-uniform sizes were engineered by a polyvinylpyrrolidone (PVP)-assisted hydrothermal method. Four different samples/morphologies of ZCO were obtained (PVP-L@6, PVP-H@6, PVP-L@12, and PVP-H@12) by altering the reaction parameters such as surfactant concentration (PVP) and reaction time, which can play a significant role in the formation of flower-/petal-/flake-like architectures. The alteration of the reaction parameters not only resulted in morphological changes but also affected the surface area, pore size/volume, crystalline nature, non-stoichiometry of Zn, Co, and O in ZCO, and their electrochemical performance. The metal (Zn/Co)/O deficiencies of ZCO samples were investigated via X-ray photoelectron spectroscopy and supported by the Rietveld refinement method. Furthermore, a plausible growth mechanism for these flower-like ZCO microstructures was projected based on the experimental results. The four dissimilar samples/morphologies of ZCO, which exhibit different electrochemical performances, were investigated. Our results show that PVP-H@12 exhibits higher specific capacitance (761/680 F g⁻¹ at 0.35/1 A g⁻¹) and good cycling constancy (90% capacitive retention after 2000 cycles at 5 Ag⁻¹) among all the four samples.     

Highly porous metal organic framework derived NiO hollow spheres and flowers for oxygen evolution reaction and supercapacitors

In this study, metal-organic-framework (MOF) derived porous NiO hollow spheres and flowers were obtained using facile solvothermal synthesis and heat treatment. After pyrolyzing, the flower like and hollow spherical like morphology of NiO nanoparticles was successfully inherited from the initial MOF-based templates. The electrochemical studies demonstrated that the porous NiO hallow spheres unveiled a better supercapacitive performance (specific capacitance (C_s) = 1058 F g^?1 at current density (j) = 2 A g^?1) and oxygen evolution reaction (OER) catalytic activity (overpotential (?) = 323 mV) compared to porous NiO flowers (C_s = 857 F g^?1 at j = 2 A g^?1 and ? = 346 mV). Moreover, excellent capacity retention of over 93% was obtained in porous NiO-hs nanoparticles even after 5000 cycles. The fabricated NiO//Fe₂O₃ asymmetric supercapacitor delivered an energy density (E) of 35.75 W h Kg^?1 under power density (P) of 780 W kg^?1 and showed promising stability over 3000 cycles. Considering the ease of preparation and high catalytic activity and supercapacitive performance, these prous NiO hallow structures can be considered as a potential electrode material for next generation energy storage devices and OER catalysts.     

Admixture Analysis Using Genotyping-by-Sequencing Reveals Genetic Relatedness and Parental Lineage Distribution in Highbush Blueberry Genotypes and Cross Derivatives

Blueberries (Vaccinium section Cyanococcus) are perennial shrubs widely cultivated for their edible fruits. In this study, we performed admixture and genetic relatedness analysis of northern highbush (NHB, primarily V. corymbosum) and southern highbush (SHB, V. corymbosum introgressed with V. darrowii, V. virgatum, or V. tenellum) blueberry genotypes, and progenies of the BNJ16-5 cross (V. corymbosum × V. darrowii). Using genotyping-by-sequencing (GBS), we generated more than 334 million reads (75 bp). The GBS reads were aligned to the V. corymbosum cv. Draper v1.0 reference genome sequence, and ~2.8 million reads were successfully mapped. From the alignments, we identified 2,244,039 single-nucleotide polymorphisms, which were used for principal component, haplotype, and admixture analysis. Principal component analysis revealed three main groups: (1) NHB cultivars, (2) SHB cultivars, and (3) BNJ16-5 progenies. The overall fixation index (F_ST) and nucleotide diversity for NHB and SHB cultivars indicated wide genetic differentiation, and haplotype analysis revealed that SHB cultivars are more genetically diverse than NHB cultivars. The admixture analysis identified a mixture of various lineages of parental genomic introgression. This study demonstrated the effectiveness of GBS-derived single-nucleotide polymorphism markers in genetic and admixture analyses to reveal genetic relatedness and to examine parental lineages in blueberry, which may be useful for future breeding plans.     

An alpha-mercaptoacrylic acid derivative is a selective nonpeptide cell-permeable calpain inhibitor and is neuroprotective

Overactivation of calcium-activated neutral protease (calpain) has been implicated in the pathophysiology of several degenerative conditions, including stroke, myocardial ischemia, neuromuscular degeneration, and cataract formation. Alpha-mercaptoacrylate derivatives (exemplified by PD150606), with potent and selective inhibitory actions against calpain, have been identified. PD150606 exhibits the following characteristics: (i) Ki values for mu- and m-calpains of 0.21 microM and 0.37 microM, respectively, (ii) high specificity for calpains relative to other proteases, (iii) uncompetitive inhibition with respect to substrate, and (iv) it does not shield calpain against inactivation by the active-site inhibitor trans-(epoxysuccinyl)-L-leucyl-amido-3-methylbutane, suggesting a nonactive site action for PD150606. The recombinant calcium-binding domain from each of the large or small subunits of mu-calpain was found to interact with PD150606. In low micromolar range, PD15O6O6 inhibited calpain activity in two intact cell systems. The neuroprotective effects of this class of compound were also demonstrated by the ability of PD150606 to attenuate hypoxic/hypoglycemic injury to cerebrocortical neurons in culture and excitotoxic injury to Purkinje cells in cerebellar slices.