Search Results (53)

Partial nitrification-Anammox (PN-A) is a cost-effective, environmentally friendly, and efficient method for removing ammonia (NH₄⁺-N) pollutants from water. However, the limited accumulation of nitrite (NO₂⁻-N) represents a bottleneck in the development of PN-A processes. To address this issue, this study developed a composite carrier loaded with nano zero-valent iron (nZVI) and zeolite to enhance NO₂⁻-N accumulation during short-cut nitrification. The modified composite carrier revealed electropositive, hydrophilicity, and surface roughness. These surface characteristics correlate positively with the carrier’s total biomass adsorption capacity; the initial adsorption of microorganisms by the composite carrier was increased by 8.7 times. Zeolite endows the carrier with an NH₄⁺-N adsorption capacity of 4.50 mg/g carrier. The entropy-driven ammonia adsorption process creates an ammonia-rich microenvironment on the surface of the carrier, providing effective inhibition of nitrite-oxidizing bacteria (NOB). In tests conducted with a moving bed biofilm reactor and a sequencing batch reactor, the composite carrier achieved a 95% NH₄⁺-N removal efficiency, a NO₂⁻-N accumulation efficiency of 78%, and a doubling in total nitrogen removal efficiency. This composite carrier enhances NO₂⁻-N accumulation by preventing biomass washout, inhibiting NOB, and enriching PN-A functional bacteria, suggesting its potential for large-scale, stable PN-A applications. Full article

(1) Background: Alzheimer’s disease (AD) is characterized by β-amyloid (Aβ) peptide accumulation and mitochondrial dysfunction during the early stage of disease. PINK1 regulates the balance between mitochondrial homeostasis and bioenergy supply and demand via the PINK1/Parkin pathway, Na⁺/Ca²⁺ exchange, and other pathways. (2) Methods: In this study, we synthesized positively charged carbon dots (CA-PEI CDs) using citric acid (CA) and polyethyleneimine (PEI) and used them as vectors to express PINK1 genes in the APP/PS1-N2a cell line to determine mitochondrial function, electron transport chain (ETC) activity, and ATP-related metabolomics. (3) Results: Our findings showed that the CA-PEI CDs exhibit the characteristics of photoluminescence, low toxicity, and concentrated DNA. They are ideal biological carriers for gene delivery. PINK1 overexpression significantly increased the mitochondrial membrane potential in APP/PS1-N2a cells and reduced reactive-oxygen-species generation and Aβ1-40 and Aβ1-42 levels. An increase in the activity of NADH ubiquinone oxidoreductase (complex I, CI) and cytochrome C oxidase (complex IV, CIV) induces the oxidative phosphorylation of mitochondria, increasing ATP generation. (4) Conclusions: These findings indicate that the PINK gene can alleviate AD by increasing bioenergetic metabolism, reducing Aβ1-40 and Aβ1-42, and increasing ATP production. Full article

The corrosion resistance of 316L cladding layers was addressed via the electrochemical test, to illustrate the coupling effect of the disconnected pores and grain morphology on the corrosion tolerance of 316L cladding layers. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and electrochemical testing were employed to characterize the microstructure, elemental distribution, phase composition, and corrosion resistance of the cladding layers. The results indicate that the disconnected porosity in the surface of the cladding layer decreased from 0.79% to 0.48% and the grain morphology underwent a transformation from equiaxed crystals to columnar and lath crystals, with the increasing scanning speed. The primary phase in the cladding layer was γ-Fe. Under the dual effect of a low disconnected porosity and grain morphology, the corrosion potential of the cladding layer became more electropositive from −568 mV_SCE to −307 mV_SCE, and the corrosion current density reduced from 4.664 μA∙cm⁻² to 1.645 μA∙cm⁻². The pitting potential improved from 0.005 V_SCE to 0.575 V_SCE as the scanning speed increased. Thus, the non-connected pores in the 316L cladding layer also affected the corrosion resistance, especially the pitting resistance. The corrosion resistance of the cladding layer can be significantly enhanced via the control of the disconnected pores and grain morphology. Full article

Herein, a chitosan film (CS) was modified using 2,3-epoxy-propyl trimethyl ammonium chloride (GTA) to flocculate granular pollutants in potato starch wastewater, aiming at the deficiencies of poor water solubility and weak electropositivity of the chitosan film. By examining the degree of substitution of chitosan film amino under different factors and different levels and response surface optimization tests, the optimum preparation conditions of chitosan film quaternary ammonium salt (HTCC) were obtained. Using scanning electron microscopy (SEM), Fourier infrared (FTIR) spectroscopy, X-ray diffraction (XRD), and ¹H-nuclear magnetic spectroscopy, the nucleophilic substitution reaction of the GTA molecule with the hydrogen atoms in the chitosan film amino group successfully improved the water solubility and electropositivity of the chitosan film. HTCC was used to treat potato starch wastewater, and the optimal flocculation conditions were obtained. The flocculation product was recovered, and the composition analysis of the flocculation product demonstrated that HTCC-potato protein flocculation precipitate was rich in high protein, which is a good choice of feed and can realize sustainable utilization of resources. Full article

The isoelectronic relationship of 1,2-azaborinine (B=N structural motif) and benzene (C=C) is well documented. Upon deprotonation of the former, the anionic 1,2-azaboratabenzene is obtained, which is isosteric with pyridine (C=N) and has a similar capability as an aromatic N-donor. We present the complexation of boron and aluminum precursors with a κ²-N,O-donating 8-hydroxy-BN-naphthalene ligand (H₂(BQ), 1). Six chelate complexes with 1:1 and 2:1 stoichiometries were isolated and characterized by X-ray diffraction analysis and NMR spectroscopy. Comparing the isosteric dimethylaluminum complexes of H₂(BQ) and an 8-hydroxyquinoline (HQ’, 2) as a reference allowed us to quantify the influence of a formal substitution of carbon by boron on the structure and the electronic properties: While the structural parameters of the ligands were similar, the electropositive boron atom affected the electron density distributions within the complexes substantially. As the consequence, the Al–N bond was significantly shortened, and the aluminum atom showed a different coordination geometry than in the quinoline analog. Moreover, strong hypsochromic shifts of both the absorption and the emission were observed. The results highlight that the differences between CN and BN polyaromatic complexes are more distinct than between equally charged BN and CC congeners. Full article

This research aimed to develop a simple and cost-effective method for fabricating electropositive membranes for highly efficient water filtration. Electropositive membranes are novel functional membranes with electropositive properties and can filter electronegative viruses and bacteria using electrostatic attraction. Because electropositive membranes do not rely on physical filtration, they exhibit high flux characteristics compared with conventional membranes. This study presents a simple dipping process for fabricating boehmite/SiO₂/PVDF electropositive membranes by modifying an electrospun SiO₂/PVDF host membrane using electropositive boehmite nanoparticles (NPs). The surface modification enhanced the filtration performance of the membrane, as revealed by electronegatively charged polystyrene (PS) NPs as a bacteria model. The boehmite/SiO₂/PVDF electropositive membrane, with an average pore size of 0.30 μm, could successfully filter out 0.20 μm PS particles. The rejection rate was comparable to that of Millipore GSWP, a commercial filter with a pore size of 0.22 μm, which can filter out 0.20 μm particles via physical sieving. In addition, the water flux of the boehmite/SiO₂/PVDF electropositive membrane was twice that of Millipore GSWP, demonstrating the potential of the electropositive membrane in water purification and disinfection. Full article

AA9 lytic polysaccharide monooxygenases (LPMOs) are copper-dependent metalloenzymes that play a major role in cellulose degradation and plant infection. Understanding the AA9 LPMO mechanism would facilitate the improvement of plant pathogen control and the industrial application of LPMOs. Herein, via point mutation, we investigated the role of glycine 2 residue in cellulose degradation by Thermoascus aurantiacus AA9 LPMOs (TaAA9). A computational simulation showed that increasing the steric properties of this residue by replacing glycine with threonine or tyrosine altered the H-bonding network of the copper center and copper coordination geometry, decreased the surface charge of the catalytic center, weakened the TaAA9-substrate interaction, and enhanced TaAA9-product binding. Compared with wild-type TaAA9, G2T-TaAA9 and G2Y-TaAA9 variants showed attenuated copper affinity, reduced oxidative product diversity and decreased substrate Avicel binding, as determined using ITC, MALDI-TOF/TOF MS and cellulose binding analyses, respectively. Consistently, the enzymatic activity and synergy with cellulase of the G2T-TaAA9 and G2Y-TaAA9 variants were lower than those of TaAA9. Hence, the investigated residue crucially affects the catalytic activity of AA9 LPMOs, and we propose that the electropositivity of copper may correlate with AA9 LPMO activity. Thus, the relationship among the amino acid at position 2, surface charge and catalytic activity may facilitate an understanding of the proteins in AA9 LPMOs. Full article

The corrosion of steel structures in coastal areas is a major issue. Therefore, in the present study, the protection against the corrosion of structural steel is carried out by depositing 100 μm thick Al and Al-5 Mg coatings using a plasma arc thermal spray process, immersing them in 3.5 wt.% NaCl solution for 41 days (d). To deposit such metals, one of the best known processes, arc thermal spray, is frequently used, but this process has severe defects and porosity. Thus, to minimize the porosity and defects of arc thermal spray, a plasma arc thermal spray process is developed. In this process, we used normal gas to create plasma instead of argon (Ar) and nitrogen (N₂) with hydrogen (H) and helium (He). Al-5 Mg alloy coating exhibited uniform and dense morphology, where it reduced more than four times the porosity compared to Al, where Mg fills the voids of the coating, resulting in greater bond adhesion and hydrophobicity. The open circuit potential (OCP) of both coatings exhibited electropositive values due to the formation of native oxide in Al, while in the case of Al-5 Mg, the coating is dense and uniform. However, after 1 d of immersion, both coatings showed activation in OCP, owing to the dissolution of splat particles from the corner where the sharp edges are present in the Al coating, while Mg preferentially dissolved in the Al-5 Mg coating and made galvanic cells. Mg is galvanically more active than Al in the Al-5 Mg coating. Due to the capacity of the corrosion products to cover the pores and defects, both coatings stabilized the OCP after 13 d of immersion. The total impedance of the Al-5 Mg coating is gradually increased and is higher than the Al, which can be attributed to the uniform and dense coating morphology where Mg dissolves and agglomerates to form globular corrosion products and deposit over the surface, thereby causing barrier protection. The defect bearing corrosion products on Al coating led to the cause having a higher corrosion rate than the Al-5 Mg coating. A total of 5 wt.% mg in the Al coating improved the corrosion rate by a rate of 1.6 times compared to the pure Al in the 3.5 wt.% NaCl solution after 41 d of immersion. Full article

The present work was aimed at identifying the IgE-binding epitopic regions on the surface of the Cup s 3 allergen from the common cypress Cupressus sempervirens, that are possibly involved in the IgE-binding cross-reactivity reported between Cupressaceae species. Three main IgE-binding epitopic regions were mapped on the molecular surface of Cup s 3, the PR-5 thaumatin-like allergen of common cypress Cupressus sempervirens. They correspond to exposed areas containing either electropositive (R, K) or electronegative (D, E) residues. A coalescence occurs between epitopes #1 and #2, that creates an extended IgE-binding regions on the surface of the allergen. Epitope #3 contains a putative N-glycosylation site which is actually glycosylated and could therefore comprise a glycotope. However, most of the allergenic potency of Cup s 3 depends on non-glycosylated epitopic peptides. The corresponding regions of thaumatin-like allergens from other closely related Cupressaceae (Cryptomeria, Juniperus, Thuja) exhibit a very similar conformation that should account for the IgE-binding cross-reactivity observed among the Cupressaceae allergens. Full article

A rational design of transition metal catalysts to achieve selective hydrogenation of furfural (FFR) to tetrahydrofurfuryl alcohol (THFA) under facile conditions is a promising option. In this work, a series of Ni catalysts were synthesized by controlled thermal treatment of Ni-based metal-organic frameworks (MOFs), with the purpose of modulating the interface of nickel nanoparticles by the reticular coordination in MOF precursors. The catalytic performance indicates that Ni/C catalyst obtained at 400 °C exhibits efficient conversion of FFR (>99%) and high selectivity to THFA (96.1%), under facile conditions (80 °C, 3 MPa H₂, 4.0 h). The decomposition of MOF at low temperatures results in highly dispersed Ni⁰ particles and interfacial charge transfer from metal to interstitial carbon atoms induced by coordination in MOF. The electron-deficient Ni species on the Ni surface results in an electropositive surface of Ni nanoparticles in Ni/C-400, which ameliorates furfural adsorption and enhances the hydrogen heterolysis process, finally achieving facile hydrogenation of FFR to THFA. Full article

In this study, an old concept of anchimeric assistance is viewed from a different angle. Primary cations with two different heteroatomic substituents in the α-position to the cationic carbon atom CHXY–CH₂⁺ (X, Y = Me₂N, MeO, Me₃Si, Me₂P, MeS, MeS, Br) can be stabilized by the migration of either the X or Y group to the cation center. In each case, the migration can be either complete, resulting in the transfer of the migrating group to the adjacent carbon atom and the formation of a secondary carbocation stabilized by the remaining heteroatom, or incomplete, leading to an anchimerically assisted iranium ion. For all combinations of the above groups, these transformations have been studied by theoretical analysis at the MP2/aug-cc-pVTZ level and were shown to occur depending on the ability of anchimeric assistance by X and Y, as well as the conformation of the starting primary carbocation. In the conformers of α-amino cations with the p-orbital, C–N bond and the nitrogen lone pair in one plane, the Me₂N group migrates to the cationic center to give aziranium ions. Otherwise, the second heteroatom is shifted to give iminium ions, without or with very slight anchimeric assistance. In the α-methoxy cations, the MeO group can be shifted to the cationic center to give the O-anchimerically assisted ions as local minima, the global minima being the ions anchimerically assisted by another heteroatom. The electropositive silicon tends to migrate towards the cationic center, but with the formation of a π-complex of the Me₃Si cation with the C=C bond rather than a Si-anchimerically assisted cation. The phosphorus atom can either fully migrate to the cationic center (X = P, Y = S, Se) or form anchimerically stabilized phosphiranium ions (X = P, Y = O, Si, Br). The order of the anchimeric assistance for the heaviest atoms decreases in the order Se >> S > Br. Full article

Experimental findings for SARS-CoV-2 related to the glycan biochemistry of coronaviruses indicate that attachments from spike protein to glycoconjugates on the surfaces of red blood cells (RBCs), other blood cells and endothelial cells are key to the infectivity and morbidity of COVID-19. To provide further insight into these glycan attachments and their potential clinical relevance, the classic hemagglutination (HA) assay was applied using spike protein from the Wuhan, Alpha, Delta and Omicron B.1.1.529 lineages of SARS-CoV-2 mixed with human RBCs. The electrostatic potential of the central region of spike protein from these four lineages was studied through molecular modeling simulations. Inhibition of spike protein-induced HA was tested using the macrocyclic lactone ivermectin (IVM), which is indicated to bind strongly to SARS-CoV-2 spike protein glycan sites. The results of these experiments were, first, that spike protein from these four lineages of SARS-CoV-2 induced HA. Omicron induced HA at a significantly lower threshold concentration of spike protein than the three prior lineages and was much more electropositive on its central spike protein region. IVM blocked HA when added to RBCs prior to spike protein and reversed HA when added afterward. These results validate and extend prior findings on the role of glycan bindings of viral spike protein in COVID-19. They furthermore suggest therapeutic options using competitive glycan-binding agents such as IVM and may help elucidate rare serious adverse effects (AEs) associated with COVID-19 mRNA vaccines, which use spike protein as the generated antigen. Full article

The natural element aluminum possesses a number of unique biochemical and biophysical properties that make this highly neurotoxic species deleterious towards the structural integrity, conformation, reactivity and stability of several important biomolecules. These include aluminum’s (i) small ionic size and highly electrophilic nature, having the highest charge density of any metallic cation with a Z²/r of 18 (ionic charge +3, radius 0.5 nm); (ii) inclination to form extremely stable electrostatic bonds with a tendency towards covalency; (iii) ability to interact irreversibly and/or significantly slow down the exchange-rates of complex aluminum–biomolecular interactions; (iv) extremely dense electropositive charge with one of the highest known affinities for oxygen-donor ligands such as phosphate; (v) presence as the most abundant metal in the Earth’s biosphere and general bioavailability in drinking water, food, medicines, consumer products, groundwater and atmospheric dust; and (vi) abundance as one of the most commonly encountered intracellular and extracellular metallotoxins. Despite aluminum’s prevalence and abundance in the biosphere it is remarkably well-tolerated by all plant and animal species; no organism is known to utilize aluminum metabolically; however, a biological role for aluminum has been assigned in the compaction of chromatin. In this Communication, several examples are given where aluminum has been shown to irreversibly perturb and/or stabilize the natural conformation of biomolecules known to be important in energy metabolism, gene expression, cellular homeostasis and pathological signaling in neurological disease. Several neurodegenerative disorders that include the tauopathies, Alzheimer’s disease and multiple prion disorders involve the altered conformation of naturally occurring cellular proteins. Based on the data currently available we speculate that one way aluminum contributes to neurological disease is to induce the misfolding of naturally occurring proteins into altered pathological configurations that contribute to the neurodegenerative disease process. Full article

The present work proposes an experimental strategy to prepare argan nutshell-derived porous carbons using potassium hydroxide (KOH). Several experimental parameters of the activation process were evaluated (temperature, impregnation ratio, and activation time), and an optimized carbon (ACK) was obtained. The surface properties of the ACK sample were determined, and the porous carbon was applied as an adsorbent of diclofenac (DCF) and paroxetine (PARX). A commercial carbon (CC) was used as a benchmark. The ACK porous carbon presented a higher surface area and micropore volume (1624 m² g⁻¹ and 0.40 cm³ g⁻¹, respectively) than CC carbon (1030 m² g⁻¹ and 0.30 cm³ g⁻¹, respectively), but the maximum adsorption capacities of DCF (214–217 mg g⁻¹) and PARX (260–275 mg g⁻¹) were comparable among the two carbons. Besides π-π interactions, H-bonds with the electronegative atoms of the adsorbate molecules and the electropositive H of the oxygen functional groups were appointed as the most probable mechanisms for adsorption onto ACK porous carbon. The electrostatic attraction was also considered, particularly for DCF with CC carbon. The pore size might have also been critical, since CC carbon presented more supermicropores (0.7–2 nm), which are usually more favorable toward the adsorption of pharmaceutical molecules. The reusability of the ACK carbon was tested up to four cycles of adsorption–desorption by using ultrasonic washing with water. The results indicated that no more than one cycle of use of ACK should be performed. Full article

Electrochemical characterization of alumina-based membranes obtained by two different techniques, sinterization or anodization, is performed by analyzing membrane potential values. This analysis allows us the estimation of the effective concentration of fixed charge in the membrane (X_ef) and the transport number of the ions into the pores (t_i), as well as the determination of ionic permselectivity (P(i)) and their correlation with the different structures (supported, symmetrical or asymmetric), geometrical parameters (pore size and porosity) and surface materials (alumina-zirconia or alumina) of the studied membranes. From these results, the electropositive character of the membranes was stated, but also the significant reduction (70%) in X_ef value and around 30% in permselectivity when pore size increases from 25 nm to 100 nm, in the case of sinterized alumina-zirconia membranes with similar porosity (CRF samples), while the clear influence of pore size on the electrochemical behavior of the electrochemically synthesized alumina membranes (NPAM samples) was confirmed as well as the lower influence of membrane porosity. Moreover, the effect of protein (BSA) static fouling on electrochemical parameters for both CRF and NPAMs samples was also analyzed, and our results show a reduction in the electropositive character of both membranes, being this behavior opposite to that discussed for one of the NPAMs as a result of surface modification with a theophylline derivative (Theo 1). Full article