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In this study we fabricated highly oxidized graphene oxides (GO) to reduce the optical bulk absorption, and to achieve a low-loss GO/silicon hybrid optical waveguide. The highly oxidized GO was fabricated using triple amount of oxidants and elongated oxidizing time via a modified Hummers’ method, together with post ozone treatment to effectively break down the C = C pi-conjugation network. The high oxidation degrees of GO were confirmed by a wide interlayer spacing (1.26 nm) in XRD patterns and a high fraction of oxygenated carbon (61.57%) observed in XPS spectra. Integrating a GO thin film on top of a silicon ring resonator revealed an extra optical loss of 1.2 dB/cm, while this value reduced to 0.8 dB/cm in a GO grating covered silicon strip waveguide. The resulting GO/silicon hybrid waveguide grating provided an extinction ratio of up to 35 dB at Bragg wavelength. We further demonstrated GO/silicon hybrid waveguide moire gratings to provide dual stopbands with a controllable stopband interval from 2.5 to 20 nm. All results validate the promising optical properties of such GO material for low-loss heterogeneous integration on silicon-on-insulator.

Lacquer wood (LW) goes through one-step and two-step H3PO4 activation process to prepare activated carbons (ACs) at different temperature, and its performance was evaluated by testing CV, EIS, GCD and cycling respect to an electrode material in supercapacitors. The performance of lacquer wood activated carbon prepared by different activation methods and temperature (300, 400, 500, 600, 700, and 800 °C) was studied, and the influence on its electrochemical properties provides valuable guidance for the high-efficient energy utilization of lacquer wood. The results showed that the AC generated via one-step activation process at 400 °C demonstrate excellent specific surface area (SBET 1609.09 m2/g) than those from two-step activation method. Besides, the biomass-derived ACs presented overall better electrochemistry characteristic than those from charcoal-derived ACs. The largest specific capacitance (354 F/g) was obtained in the ACs-based electrodes which was generated from one-step activation process (activated at 600 °C). After 10000 cycles, its capacity retention reached 95.3%, which provides a meaningful guidance into the application of energy storage supercapacitors. This study proves that the LW derived ACs are promising electrodes of the high-performance supercapacitors, which is beneficial for value-added and industrial supercapacitors application of lacquer wood ACs.

Juncus effusus L. (J. effusus) is a Traditional Chinese Medicine (TCM) that has long been used for dealing with gynaecological disorders, such as relieving insomnia, preventing tinnitus, reducing edema with diuretic effect. In our course of evidence-based medical research focused on this herb, one new phenanthrene, Junfusol B (2), together with seventeen known compounds were isolated and identified. All the structures of these compounds were elucidated by spectroscopic methods. The absolute stereochemistry of compounds 1 and 2 was further determined by comparing their calculated and experimental Electronic Circular Dichroism (ECD) spectra and optical rotation (OR) values. The isolates were evaluated for their estrogenic and anti-inflammatory activities which were considered as relevant etiological factors of insomnia, tinnitus and edema in the ancient TCM theory. The results revealed that most of the obtained phenanthrenes in this work were found exerting agonistic effects on estrogen receptor. This is the first report to declare the exact estrogen-regulating potential among this type of compounds from J. effusus. Moreover, phenanthrenes 3 - 7 exhibited significant inhibitions on superoxide anion generation and elastase release in fMLP/CB-induced human neutrophilic inflammation model. J. effusus may be developed as a complementary agent utilized in menopausal multiple syndromes.

Aging is a natural process that will cause physiological changes in organs. The effects of djulis and green caviar in skincare are currently unclear. This study combined hydrolyzed collagen with djulis and green caviar to develop new functional formulas that improve skin parameters. Fifty subjects were randomly assigned and divided into a placebo group (n=25) and a collagen drink group (n=25), and gave 50 ml of collagen of a collagen drink or placebo drink daily for 28 days, and we examined skin moisture, elasticity, gloss, spot, wrinkle, roughness, smoothness, pore, collagen and erythema. We find that intake of collagen drinks group improved skin parameters at 14 days and 28 days compared with baseline (0 day). The collagen drinks group improved skin parameters at 28 days compared with the placebo group. This clinical study proved the combination of collagen with djulis and green caviar for the substantial improvements in moisture, elasticity, gloss, spot, wrinkle, roughness, smoothness, pore, collagen, and erythema in the skin.

Purpose Population aging was a global trend, and the most obvious thing after aging was the change in skin appearance. Therefore, the active ingredients that delay skin aging were particularly noticed. Past studies had pointed out that Chinese herbal extracts can improve skin elasticity, reduce wrinkles and melanin precipitation. The purpose of this paper is to explore whether combining hydrolyzed collagen with Chinese herbal extracts can improve skin conditions and achieve anti-inflammatory effects. Design/methodology/approach Fifty subjects were randomly divided into collagen or placebo groups, and one bottle of collagen or placebo drink was used every day for four weeks, after which skin and inflammatory factors were tested. Findings In comparison with the baseline results, the skin parameters were improving after four-week intervention. In addition, the IL-6, IL-8, TNF-a were significantly decreased and tissue inhibitor matrix metalloproteinase 1 (TIMP-1) was increased after four-week hydrolyzed collagen intervention. Originality/value This study showed that hydrolyzed collagen combined with Chinese herbal extracts can improve the condition of the skin, and can also reduce inflammatory associated factors, thereby achieving anti-aging effects.

Understanding the physicochemical properties and heterogeneous processes of aerosols is key not only to elucidate the impacts of aerosols on the atmosphere and humans but also to exploit their further applications, especially for a healthier environment. Experiments that allow for spatially control of single aerosol particles and investigations on the fundamental properties and heterogeneous chemistry at the single-particle level have flourished during the last few decades, and significant breakthroughs in recent years promise better control and novel applications aimed at resolving key issues in aerosol science. Here we propose graphene oxide (GO) aerosols as prototype aerosols containing polycyclic aromatic hydrocarbons, and GO can behave as two-dimensional surfactants which could modify the interfacial properties of aerosols. We describe the techniques of trapping single particles and furthermore the current status of the optical spectroscopy and chemistry of GO. The current applications of these single-particle trapping techniques are summarized and interesting future applications of GO aerosols are discussed.

The release characteristics of a unique blend of carotenoid beadlets designed to increase bioavailability were tested using the dynamic gastrointestinal model TIM‐1. Individual carotenoid bioaccessibility peaks were observed over approximately 3–4 hr in the order of lutein and zeaxanthin first, followed by lycopene, and then finally α‐ and β‐carotene; when tested as a beadlet blend or when the beadlets were compressed into tablets. Bioaccessibility measurements of 7%–20% were similar to those previously reported in literature and comparable between the two formulations, beadlet blend and tablet formulations. Total recovery of carotenoids from all compartments ranged from 70% to 90% for all carotenoids, except lycopene where almost 50% was unrecoverable after digestion in the TIM system., The release characteristics of a unique blend of carotenoid beadlets designed for increased bioavailability were tested using the dynamic gastrointestinal model TIM‐1. Peak bioaccessibility measurements separated over approximately 3–4 hr in the order of lutein and zeaxanthin first, followed by lycopene, and then finally alpha and beta carotene; both when tested as a beadlet blend alone and when tested as compressed tablets.

Solar-driven hydrogen peroxide (H2O2) production presents unique merits of sustainability and environmental friendliness. Herein, efficient solar-driven H2O2 production through dioxygen reduction is achieved by employing polymeric carbon nitride framework with sodium cyanaminate moiety, affording a H2O2 production rate of 18.7 μmol h −1 mg−1 and an apparent quantum yield of 27.6% at 380 nm. The overall photocatalytic transformation process is systematically analyzed, and some previously unknown structural features and interactions are substantiated via experimental and theoretical methods. The structural features of cyanamino group and pyridinic nitrogen-coordinated soidum in the framework promote photon absorption, alter the energy landscape of the framework and improve charge separation efficiency, enhance surface adsorption of dioxygen, and create selective 2e− oxygen reduction reaction surface-active sites. Particularly, an electronic coupling interaction between O2 and surface, which boosts the population and prolongs the lifetime of the active shallow-trapped electrons, is experimentally substantiated., Solar-driven H2O2 production presents a renewable approach to chemical synthesis. Here, authors perform a mechanistic analysis on the contribution of the sodium cyanaminate moiety to the 2-electron oxygen reduction reaction performance of polymeric carbon nitride frameworks.

Exfoliated and plicated g-C3N4 nanosheets (CNsF) were prepared through a thermal-chemical exfoliation in which the bulk g-C3N4 was obtained first under thermal exfoliation, and then was exposed to an acidic etching using hydrofluoric acid under hydrothermal condition. The acidic etching not only exfoliated g-C3N4 nanosheets by disrupting weak van der Waals forces between layers, which led to formation of a monolayer or a few layers of g-C3N4 nanosheets, but also made disordered defects on its surface and created plicated g-C3N4 nanosheets. Under visible-light illumination, the optimized sample (CNsF-6%) showed a hydrogen evolution rate of 54.13 μmol h−1g−1 (without co-catalyst) and a specific surface area of 121.4 m2 g−1, which were about 4.7 and 2.5 times, respectively, higher than pristine g-C3N4. It also showed remarkably enhanced photocatalytic performance in removing various organic pollutants. This remarkable improvement probably arises from the porous nanosheets and an increased number of active sites resulting from the CNsF, which subsequently enhanced the charge separation efficiency. This work provided an alternative way to obtain highly active g-C3N4 photocatalysts.

This study aimed to investigate the value and feasibility of combining fractional anisotropy (FA) values from diffusion tensor imaging (DTI) and total kidney volume (TKV) for the assessment of kidney function in chronic kidney disease (CKD). Fifty-one patients were included in this study. All MRI examinations were performed with a 3.0 T scanner. DTI was used to measure FA values, and TKV was obtained from DTI and T2-weighted imaging (T2WI). Patients were divided into three groups (mild, moderate, severe) according to eGFR, which was calculated with serum creatinine. Differences in the FA values of the cortex and medulla were analysed among the three groups, and the relationships of FA values, TKV, and the product of the FA values and TKV with eGFR were analysed. Receiver operating characteristic (ROC) curve analysis was used to compare the diagnostic efficiency of the FA values, TKV, and the product of the FA values and TKV for kidney function in different CKD stages. Medullary FA values (m-FA), TKV, and the product of the m-FA values and TKV (m-FA-TKV) were significantly correlated with eGFR (r = 0.653, 0.685, and 0.797, respectively; all P

The interchangeable operation of alkaline oxygen evolution and reduction using bifunctional electrocatalysts in devices consolidates the commercialization milestone of energy storage in hydrogen, a...

Sulfamates and sulfamides are prevalent in biological molecules, but their universal synthetic methods are limited. We herein report a sulfamoylation agent with high solubility and shelf stability. Various sulfamates and sulfamides can be synthesized directly from alcohols or amines by employing this agent with high selectivity and high yields. This protocol was also successfully used for late-stage sulfamoylation of pharmaceuticals containing a hydroxyl or amino group.

Tea (Camellia sinensis (L.) O. Kuntze) is predominantly grown in acidic soils with severe limitations of P-nutrition. The present study evaluated the effects of an arbuscular mycorrhizal (AM) fungus, Claroideoglomus etunicatum, on root morphology, leaf and root P concentration, phosphatase activity in soils and roots, and the relative expression of root P transporter genes (PT1 and PT4) in Camellia sinensis ‘Fuding Dabaicha’ seedlings in sands under two levels of P viz., 0.5 μM (P0.5) and 50 μM (P50) through Hoagland solutions (pH 4.2) for 24 weeks. Under both P0.5 and P50 conditions, AM seedlings displayed a higher growth performance (shoot biomass, root biomass, and plant height), root morphology (total length, taproot length, 2nd- and 3rd-lateral root number, and volume), and root-hair length, but lower root-hair density than non-AM seedlings. Mycorrhizal inoculation significantly increased root P concentrations in P0.5 and P50 and leaf P concentrations in P0.5 over non-mycorrhizal treatment. The AM seedlings recorded considerably higher soil acid, neutral, and total phosphatase activity under P0.5 treatment, and soil neutral and total phosphatase activity under P50 treatment, compared with the non-AM seedlings. Root acid phosphatase activity was reduced due to mycorrhization at both of P0.5 and P50. AM fungal inoculation up-regulated the relative expression of root CsPT1, while down-regulated the CsPT4 expression in P0.5 and P50 treatments. It was concluded that AM fungal inoculation significantly promoted P acquisition capacity of tea plants, especially in roots through improving root growth and enhancing soil acid phosphatase activity and root CsPT1 expression.

Many Chinese herbal medicines have been proven to have anti-inflammatory effects. Among them, edible and medicinal mushrooms are rich in a variety of physiologically active ingredients, which can enhance immunity and are good materials for the development of health foods. This article aims to investigate the beneficial effects of SOD Light, a herbal formula consisting of Sparassis crispa, Aureobasidium pullulan, and Ganoderma lucidum, on anti-inflammation, antioxidant, and immune-modulation. SOD Light was able to inhibit ROS expression level and boost the SOD activity in PBMCs by 11% and 43.8%, respectively, as compared with the control group, and the significant improvement effect of the phagocytic activity of neutrophils was exhibited. Moreover, SOD Light also significantly enhanced the expression of the lymphocyte development-associated and adaptive immune-related genes (i.e., CD134, CD26, CD96, CD247, and IL-16). This study successfully unveils that the combination of S. crispa, A. pullulans, and G. lucidum was available for anti-oxidation, cytokines production, enhancement of T cell activation, and lymphocyte development in PBMCs, which implies that SOD Light are beneficial for immune modulation.

In this work, an experiment was carried out to investigate the preparation condition of anisotropic Fe-deficient M-type Ca–Sr–La system ferrite with optimum magnetic and physical properties using the raw material Fe2O3 from steel industrial iron oxide waste. The compositions of the calcined ferrites were chosen according to the stoichiometry ${\mathrm {Ca}}_{1-x-y}$ La x Sr y Fe10.9CozO19, where M-type single-phase calcined powder was synthesized with a composition of $x = 0.45$ , $y = 0.18$ , and $z= 0$ . The effect of CaO, SiO2, and Co3O4 inter-additives on the Ca–Sr–La system ferrite was also discussed in order to obtain low-temperature sintered magnets. The magnetic properties of $B_{r} = 4570$ Gauss, $_{b}H_{c} = 4320$ Oe, $_{i}H_{c} = 5260$ Oe, and ( $BH$ ) $_{\mathrm {max}}= 5.16$ MGOe were obtained for Ca–Sr–La system hard magnets with low cobalt content at 1.85 wt%. The magnetic properties of the prepared magnets really good compared to that of the traditional Sr–La–cobalt (Co) M-type ferrite, which has been the highest grade M-type hard ferrite. The remarkable steel industrial iron oxide waste Fe2O3 is recycled to produce high-end permanent magnets under an output power of < 1 kW, which will eventually be used in high-efficiency motors.

Only a few known epoxide hydrolases (EHs) displayed activity towards o-nitrostyrene oxide (4a), presumably owing to the large steric hindrance caused by o-nitro substituent. Therefore, excavating EHs with high activity and enantio- and/or regio-selectivity towards racemic (rac-) 4a is essential but challenging. Here, AuEH2 from Aspergillus usamii was expressed in E. coli BL21(DE3). E. coli/Aueh2, an E. coli transformant expressing AuEH2, possessed EH activities of 16.2–184 U/g wet cell towards rac-styrene oxide (1a) and its derivatives (2a–13a), and the largest enantiomeric ratio of 96 towards rac-4a. The regioselectivity coefficients, βR and βS, of AuEH2 were determined to be 99.2% and 98.9%, suggesting that it regiopreferentially attacks the Cβ in the oxirane rings of (R)- and (S)-4a. Then, the nearly perfect kinetic resolution of 20 mM rac-4a in pure water was carried out using 20 mg/mL wet cells of E. coli/Aueh2 at 25 °C for 50 min, retaining (S)-4a with over 99% ees and 48.9% yields, while producing (R)-o-nitrophenyl-1,2-ethanediol (4b) with 95.3% eep and 49.8% yieldp. To elucidate the molecular mechanism of AuEH2 with high enantiopreference for (R)-4a, its crystal structure was solved by X-ray diffraction and the molecular docking of AuEH2 with (R)- or (S)-4a was simulated.

Excessive energy consumption and low reaction efficiency caused by electron cycle rate limitations are bottlenecks in water treatment. Here, we introduce an innovative strategy to overcome this problem via constructing a novel three-dimensional (3D) hybrid of vanadium tetrasulfide cross-linking graphene-like carbon with π electrons (VSO–C(π)), which exhibits excellent performance during refractory pollutant removal based on sustainable electron cycling between hydrogen peroxide (H2O2), dissolved oxygen (DO), and pollutants at the solid–liquid micro-interface. VSO–C(π) is synthesized through an in situ hydrothermal synthesis procedure and characterized via a series of techniques. The cation-π structures are constructed through V–S–C(π) and V–O–C(π) bridges in VSO–C(π), triggering orientable electron transfer from C(π) to the metal V centers and forming a polarized distribution of surface electrons. In the VSO–C(π)/pollutants/DO/H2O2 system, the pollutants act as electron donors to C(π), with the subsequent degradation of pollutants, while DO and H2O2 act as electron acceptors and are activated by reactive oxygen species to further degrade the pollutants at the V centers. This sustainable electron cycling process is responsible for the excellent activity and superior adaptability to pH changes and different salt environments, while also greatly saving resources and reducing energy consumption.

In this study, we investigated the stress and doping effects of ferroelectric hafnium zirconium oxide (HfZrO) based on material analysis and electrical characteristics. The experimental results revealed that the ferroelectric crystalline phase is effectively transferred by mechanical stress of tantalum nitride (TaN) electrodes, and the origin of stress is mainly the thermal residual stress formed near the TaN and HfZrO interface. The ferroelectric polarization characteristics of HfZrO can be further modified by additional Al doping, which not only improves the leakage current of HfZrO due to the large bandgap of Al2O3 but also simultaneously stabilizes the ferroelectric domain switching under a large coercive field.

Tungstic oxide (WO3) is a promising visible-light-responsive photoanode material, but it has poor charge transport and collection properties. In this study, a WO3/BiFeO3 core/shell photoanode (WO3/BFO) with enhanced photoelectrochemical (PEC) performance was successfully prepared using a facile spin-coating method. The optimal WO3/BFO shows an excellently enhanced and stable photocurrent density of ∼2.83 mA cm−2 at 0.6 V vs. Ag/AgCl, which is ∼244% more than WO3 under AM 1.5 illumination. The results of Mott–Schottky tests, intensity modulated photoelectrochemical spectroscopy and transient photocurrent decay indicated that the BFO ferroelectric nanolayer significantly enhances the charge density of the WO3/BFO, and improves its charge transport and separation property and charge lifetime, which could be the reason for the enhanced PEC activity of WO3/BFO.

Protein oxidation is a critical process in the deterioration and spoilage of fish and related commodities during processing and storage. In this study, the hydroxyl radical generation system (HRGS) was used to simulate the effect of oxidation on the functional, conformational and gelling properties of topmouth culter (Culter alburnus) myofibrillar proteins (MP). Additionally, the effects of oxidation on the gel-forming abilities of MP were also systematically analyzed from the perspective of intermolecular interaction forces. Oxidation was shown to decrease the total sulfhydryl content, increase the surface hydrophobicity, and induce conformational changes in MP. Rheological analysis showed that oxidation reduced the gel strength. Water holding capacity (WHC) and low-field nuclear magnetic resonance (LF-NMR) analyses showed that low oxidation could enhance water binding of protein matrix, while high-degree oxidation could substantially reduce the gelling properties of MP. The selective solubility of MP gel proved that oxidation could reduce the content of ionic and hydrogen bonds and increase hydrophobic interactions. All the results indicate that oxidation could alter the intermolecular interactions between protein-protein and protein-water molecules, due to irregular unfolding and inhibition of the cross-linking of amino acid side chains, leading to reduction in the quality and function of fish and related products.

The search for high-active and long-lasting materials is of paramount significance for elimination of aqueous organic contaminants. Herein, a nitrogen-coordinated cobalt embedded in hollow carbon p...

In this study, a novel BiOBr/HPW/Au photocatalyst was prepared via hydrothermal method followed by photo-reduction method. The characterization results indicated the successful introduction of HPW and Au in BiOBr. BiOBr/HPW/Au exhibited excellent photocatalytic activity in RhB degradation. The degradation rate constant of BiOBr/HPW/Au was 3.55 times higher than that of BiOBr. Radical scavenger experiments showed that ·O−2 was the dominant reactive radical species. A possible mechanism of the enhanced photocatalytic activity was attributed to the synergistic effect of BiOBr, HPW and Au, which resulted in enhanced quantum efficiency and high light harvesting efficiency.

Long-term efficient separation of highly emulsified oily wastewater is challenging. Reported herein is the preparation of a reinforced superhydrophilic, underwater superoleophobic membrane with demulsification properties using active iron nanoparticles in situ generated on a polydopamine (PDA)/polyethylenimine (PEI)-modified polyvinylidene fluoride (PVDF) membrane surface. A stable zwitterionic structure is fabricated on the membrane surface and provides it with an excellent capability of binding a hydration layer, leading to enhanced superhydrophilic/underwater superoleophobic properties. The interaction between the membrane surface and water is quantified using the relaxation time of water. After iron nanoparticles in situ anchoring, the superhydrophilic, underwater superoleophobic PDA/PEI modified PVDF membrane shows more stable flux behaviors, higher oil separation efficiency, demulsification, and excellent antioil-fouling properties for various anionic, nonionic, and cationic surfactant-stabilized oil-in-water emulsions in a crossflow filtration system. The reinforced hydration layer and the amphoteric charged demusification properties of the membrane play important roles in enhancing the membrane separation performance. The reinforced membrane also exhibits excellent cleaning and reusability performance in long-term operations. The outstanding separation performance, as well as the simple and cost-effective fabrication process of the membrane with various favorable properties, highlight its promise in practical emulsified oily water applications.

The objective of the study was to explore the formation mechanism and thermodynamic properties of chitosan (CS)–potato protein isolate (PPI) complex under DHPM treatment. The transmission electron microscopic (TEM) results showed the formation of a complex between CS and PPI. Meanwhile, particle size and zeta-potential were shown to increase with increasing CS concentration, further confirming the formation of the complex. The surface hydrophobicity results showed CS was bound to PPI by hydrogen bond. The ultraviolet and fluorescence spectral analysis exhibited CS formed a protective mechanism against PPI destruction, preventing the exposure of tyrosine and tryptophan residues. Infrared spectrum and circular dichroism spectral analysis revealed no occurrence of chemical reaction between CS and PPI under DHPM treatment, further indicating that they are bound by hydrogen bond and hydrophobic interaction. Moreover, CS addition was shown to enhance the intermolecular interaction and promote the formation of intermolecular hydrogen bond network. Differential scanning calorimetry (DSC) and thermo gravimetric analysis (TGA) revealed that CS addition could improve the thermal stability of PPI. These results have shed light on the formation mechanism and thermodynamic properties of the CS/PPI complex and facilitate its application in food industry.

Galvanic replacement (GR) is a widely used method to obtain substrates with nanostructure morphologies. However, substantial challenges related to the uniformity of the deposited nanostructures, th...

In order to provide more alternative epoxide hydrolases for industrial production, a novel cDNA gene Rpeh-encoding epoxide hydrolase (RpEH) of Rhodotorula paludigena JNU001 identified by 26S rDNA sequence analysis was amplified by RT-PCR. The open-reading frame (ORF) of Rpeh was 1236 bp encoding RpEH of 411 amino acids and was heterologously expressed in Escherichia coli BL21(DE3). The substrate spectrum of expressed RpEH showed that the transformant E. coli/Rpeh had excellent enantioselectivity to 2a, 3a, and 5a–10a, among which E. coli/Rpeh had the highest activity (2473 U/g wet cells) and wonderful enantioselectivity (E = 101) for 8a, and its regioselectivity coefficients, αR and βS, toward (R)- and (S)-8a were 99.7 and 83.2%, respectively. Using only 10 mg wet cells/mL of E. coli/Rpeh, the near-perfect kinetic resolution of rac-8a at a high concentration (1000 mM) was achieved within 2.5 h, giving (R)-8a with more than 99% enantiomeric excess (ees) and 46.7% yield and producing (S)-8b with 93.2% eep and 51.4% yield with high space-time yield (STY) for (R)-8a and (S)-8b were 30.6 and 37.3 g/L/h.

The diaryl ureas are very important fragments in medicinal chemistry. By means of computer-aided design, 1-aryl-3-[4-(pyridin-2-ylmethoxy)phenyl]urea derivatives were designed and synthesized, and evaluated for their antiproliferative activity against A549, HCT-116, PC-3 cancer cell lines, and HL7702 human normal liver cell lines in vitro by using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide colorimetric assay. Most of the target compounds demonstrate significant antiproliferative effects on all the selective cancer cell lines. The calculated IC50 values were reported. The target compound 1-(4-chlorophenyl)-3-{4-{[3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methoxy}phenyl}urea (7u) demonstrated the most potent inhibitory activity (IC50 = 2.39 ± 0.10 μM for A549 and IC50 = 3.90 ± 0.33 μM for HCT-116), comparable to the positive-control sorafenib (IC50 = 2.12 ± 0.18 μM for A549 and IC50 = 2.25 ± 0.71 μM for HCT-116). Conclusively, 1-aryl-3-[4-(pyridin-2-ylmethoxy)phenyl]urea derivatives as the new anticancer agents were discovered, and could be used as the potential BRAF inhibitors for further research.

Background Potato powder, a rich source of high-quality protein and starch, plays an important role in the production of functional foods. In this study, ball-mill processed potato powders with different particle sizes (278, 208, 129, and 62 μm) were analyzed in terms of physicochemical, pasting, rheological, and digestive properties. Results Scanning electron microscopy and laser diffraction analysis of the samples revealed mono-model particle-size distributions. X-ray diffraction analysis confirmed structure destruction of starch pellets. Proximate composition and physical property analysis showed an increase in the water, ash, protein, and starch content. Meanwhile, the water solubility index and swelling power values were found to increase with decreasing grain size, and so were the brightness (L*) and redness (b*) values of the potato powders. With particle size reduced to 129 μm, large changes were observed in gelatinization properties, such as peak viscosity, trough viscosity, breakdown viscosity, and final viscosity. Oscillatory rheology results also showed that, with the decrease in particle size, the storage modulus (G') and loss modulus (G″) improved, with highest storage modulus (G') observed in the 129 μm particle size. The hydrolysis rate and glycemic index also increased in the 129 μm potato powder. Conclusion The results provide information that could be useful for improving quality characteristics by using specific grain sizes in the development of potato-based products such as gluten-free products and ethnic food products with particular functional and rheological properties. © 2020 Society of Chemical Industry.

An open reading frame of sleh1, a gene encoding for a novel epoxide hydrolase from Solanum lycopersicum (SlEH1), was amplified by RT-PCR and expressed in E. coli BL21(DE3). The substrate spectrum assay showed that E. coli/sleh1 had EH activities towards all tested substrates except for racemic (rac-) 5a, and the highest enantiomeric ratio (E > 200) towards rac-2a, retaining (R)-2a with 99.1% ees and 49.2% yields and affording (R)-2b with 89.8% eep and 46.7% yieldp. Besides, E. coli/sleh1 also hydrolyzed of rac-7a–9a with moderate regioselectivities, producing (S)- or (R)-7b–9b with 40.5–51.3% eep and 69.4–75.2% yieldp. The pH optimum and stability of the purified SlEH1 were 7.5 and at a range of 6.5–8.5, and it was thermostable at or below 40 °C. Its catalytic efficiency (kcatS/KmS = 7.49 mM−1 s−1) for (S)-2a was much higher than that for (R)-2a. The gram-scale kinetic resolution of 150 mM rac-2a was carried out by E. coli/sleh1 at 20 °C for 8 h, producing (R)-2a with 98.2% ees and 45.3% overall yields after purification by silica gel column chromatography. Furthermore, the source of extremely high enantioselectivity of SlEH1 towards rac-2a was analyzed by molecular docking simulations.

Sodium hypochlorite (NaClO) solution is a typical cleaning agent for membrane fouling. However, it can damage membrane chemical structures and produce toxic disinfection byproducts, which in turn reduces the membrane performance. This study focuses on the fabrication of active membranes thereby overcoming the limitations of chemical cleaning. A hierarchical active poly(vinylidene fluoride) membrane with polydopamine/polyethyleneimine (PEI) co-supported iron nanoparticle (Fe NP) catalysts was successfully constructed and denoted as a Fe-HP-membrane. The Fe-HP-membrane exhibited excellent advanced oxidation activity with maximum flux recoveries (∼85% with bovine serum albumin [BSA] and ∼95% with humic acid [HA] solutions). After the static experiment of ∼30 days, the BSA proteins and HA successfully desorbed from the membrane surface. Especially, with a trace amount of hydrogen peroxide (H2O2) flowing over the surface of the Fe-HP-membrane, highly exposed active sites were observed. Membrane cleaning showed that the "outside-to-in" active surfaces generated considerable amounts of •OH radicals at the interface of BSA or HA and the fouled membrane. As a result, the unwanted foulants were successfully removed from the membrane interface, enabling multiple use of the Fe-HP-membrane. Therefore, backwashing with a small amount of H2O2 (0.33 wt %) covered ∼20% of the flux. In contrary, backwashing with NaClO (1 wt %) can only achieve a flux recovery of ∼10% after six consecutive BSA filtration cycles. The Fe-HP-membrane exhibited better HA foulant removal (a flux recovery of ∼51%) after backwashing with H2O2 than using NaClO (a flux recovery of ∼43%). Our findings demonstrate a new platform for water treatment and regeneration of fouled membranes.

To realize coenzyme regeneration in the reduction of haloketones, a codon-optimized gene Sygdh encoding glucose 1-dehydrogenase (SyGDH) was synthesized based on the putative GDH gene sequence (Ta0897) in Thermoplasma acidophilum genomic DNA, and expressed in E. coli BL21(DE3). Recombinant SyGDH was purified to homogeneity by affinity chromatography with the specific activity of 86.3 U/mg protein towards D-glucose at the optimum pH and temperature of 7.5 and 40 °C. It was highly stable in a pH range of 4.5–8.0 and at 60 °C or below, and resistant to various organic solvents. The Km and catalytic efficiency (kcat/Km) of SyGDH towards NADP+ were 0.67 mM and 104.0 mM−1 s−1, respectively, while those towards NAD+ were 157.9 mM and 0.64 mM−1 s−1, suggesting that it preferred NADP+ as coenzyme to NAD+. Additionally, using whole cells of E. coli/Sygdh-Sys1, coexpressing SyGDH and carbonyl reductase (SyS1), as the biocatalyst, the asymmetric reduction of 60 mM m-chlorophenacyl chloride coupled with the regeneration of NADPH in situ was conducted in DMSO/phosphate buffer (2:8, v/v) system, producing (R)-2-chloro-1-(3-chlorophenyl)ethanol with over 99.9% eep and 99.2% yield. Similarly, the reduction of 40 mM α-bromoacetophenone in n-hexane/buffer (6:4, v/v) biphasic system produced (S)-2-bromo-1-phenylethanol with over 99.9% eep and 98.3% yield.

Adlay (Coix lacryma-jobi var. ma-yuen (Rom. Caill.) Stapf) seeds are edible crop classified as Traditional Chinese Medicine (TCM). Adlay bran (AB) is one of the wastes generated during adlay refining processes. In this work, supercritical fluid extract of AB (AB-SCF) was investigated to reveal its lipid regulating potential and decode its bifunctional ingredients. AB-SCF×0.5 (30.84 mg/kg/body weight), AB-SCF×1 (61.67 mg/kg/BW), AB-SCF×5 (308.35 mg/kg/BW) and AB-SCF×10 (616.70 mg/kg/BW) were administrated to high fat-diet (HFD) induced hyperglycemic hamsters for 8 weeks. The results indicates that AB-SCF displays a prevention of dramatic body weight gains, lower levels of serum TG, TC, LDL-C and higher in HDL-C, amelioration of cardiovascular risk, alleviation of hepatic TG, TC and lipid peroxidation, and enhancement on cholesterol metabolism with higher bile acid excretion. Investigations on energy metabolic mechanism demonstrates that the hyperlipidemia mitigating capacities of AB-SCF are up-regulated on lipoprotein lipase, AMPK, p-AMPK and down-regulated at fatty acid synthase. Major bio-functional lipid compositions are identified as linoleic acid (28.59%) and oleic acid (56.95%). Non-lipid chemical and active markers are confirmed as 3-O-(trans-4-feruloyl)-β-sitostanol (1463.42 ppm), 3-O-(cis-4-feruloyl)-β-sitostanol (162.60 ppm), and β-sitosterol (4117.72 ppm). These compositions might synergistically responsible for the mentioned activities and can be regarded as analytical targets in quality control. AB-SCF may be considered as a promising complementary supplement, and developed as a functional food or new botanical drug in the future.

Structural and biochemical studies elucidate that PAN may contribute to the host protein shutdown observed during influenza A infection. Thus, inhibition of the endonuclease activity of viral RdRP is an attractive approach for novel antiviral therapy. In order to envisage structurally diverse novel compounds with better efficacy as PAN endonuclease inhibitors, a ligand-based-pharmacophore model was developed using 3D-QSAR pharmacophore generation (HypoGen algorithm) methodology in Discovery Studio. As the training set, 25 compounds were taken to generate a significant pharmacophore model. The selected pharmacophore Hypo1 was further validated by 12 compounds in the test set and was used as a query model for further screening of 1916 compounds containing 71 HIV-1 integrase inhibitors, 37 antibacterial inhibitors, 131 antiviral inhibitors and other 1677 approved drugs by the FDA. Then, six compounds (Hit01–Hit06) with estimated activity values less than 10 μM were subjected to ADMET study and toxicity assessment. Only one potential inhibitory ‘hit’ molecule (Hit01, raltegravir’s derivative) was further scrutinized by molecular docking analysis on the active site of PAN endonuclease (PDB ID: 6E6W). Hit01 was utilized for designing novel potential PAN endonuclease inhibitors through lead optimization, and then compounds were screened by pharmacophore Hypo1 and docking studies. Six raltegravir’s derivatives with significant estimated activity values and docking scores were obtained. Further, these results certainly do not confirm or indicate the seven compounds (Hit01, Hit07, Hit08, Hit09, Hit10, Hit11 and Hit12) have antiviral activity, and extensive wet-laboratory experimentation is needed to transmute these compounds into clinical drugs.