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Sugar composition not only affects fruit flavor but is also an important determinant of fruit taste and consumer preference. In this study, changes in the sugar content and sugar-metabolizing enzymes were investigated from different sections of various fruit development phases of ‘Hongshuijing’ pitaya (Hylocereus monacanthus). Genes related to sugar metabolism were also screened by transcriptome analyses. The results indicated that glucose was the major sugar in mature pitaya fruit, and was mainly regulated by vacuolar acid invertase (VAI) and sucrose synthase (SS) (degradative direction). Sugar accumulation varied in pulp between different sections of the pitaya fruit. VAI, neutral invertase (NI) and SS (degradative direction) are crucial enzymes for sugar accumulation in pitaya. The expression of 17 genes related to sucrose metabolism and obtained from seven databases [NCBI non-redundant protein database (Nr), NCBI non-redundant nucleotide sequence database (Nt), EuKaryotic Orthologous Groups (KOG), The Protein Families (Pfam), Kyoto Encyclopedia of Genes and Genomes (KEGG), Swiss-prot, and Gene Ontology (GO)] were analyzed in different pitaya pulp sections. HpVAI1 had the highest relative expression level on the 29th day after pollination (DAP). Positive correlations were found between HpVAI1 expression and VAI activity; HpNI4 and NI activity; HpSS2, HpSS5, and SS activity (synthetic direction), indicating that HpVAI1, HpNI4, and HpSS2 and HpSS5 were involved in the regulation of VAI, NI, and SS (synthetic direction), respectively. HpVAI1 and HpNI4 regulated sucrose degradation and the accumulation of glucose and fructose, while HpSS2 and HpSS5 regulated sucrose synthesis. These results suggest that HpVAI1 plays a key role in sugar metabolism during fruit development of ‘Hongshuijing’ pitaya. The results of this study provide new information about sugar metabolism in pitaya fruit that could help improve fruit quality and the breeding of new cultivars.

Designing highly efficient non-precious based electrocatalysts for oxygen reduction reaction (ORR) is of significance for the rapid development of metal-air batteries. Herein, a hydrothermal-pyrolysis method is employed to fabricate Fe, N co-doped porous carbon materials as effective ORR electrocatalyst through adopting graphitic carbon nitride (g-C3N4) as both the self-sacrificial templates and N sources. The g-C3N4 provides a high concentration of unsaturated pyridine-type N to coordinate with iron to form Fe-N active sites. Through adjusting the Fe doping amounts, it is proved that appropriate Fe doping content is conducive to the construction of abundant defects and active sites of Fe-N. The as-prepared catalyst exhibits superior electrocatalytic ORR performance in alkaline media with half-wave potential (E1/2 = 0.82 V) and onset potential (Eonset = 0.95 V), equivalent to the commercial Pt/C catalyst. Moreover, there is almost no activity loss after 10 k continuous cyclic voltammetry cycles and methanol tolerance, indicating the excellent durability and superior methanol tolerance. Remarkably, when assembled as the cathode in a Zn-air battery, the device displays a power density of 99 mW/cm2, an open-circuit potential of 1.48 V and long-term discharge-charge cycling stability, indicating the promising potential to substitute the Pt catalyst for practical application.

BACKGROUND: To evaluate the segmental myocardial extracellular volume (ECV) fraction and to define a threshold ECV value that can be used to distinguish positive late gadolinium enhancement (LGE) segments from negative myocardial segments using dual-layer spectral detector computed tomography (SDCT), with magnetic resonance imaging (MRI) as a reference. METHODS: Fifty-six subjects with cardiac disease or suspected cardiac disease, underwent both late iodine enhancement on CT (CT-LIE) scanning and late gadolinium enhancement on MRI (MRI-LGE) scanning. Each procedure occurred within a week of the other. Global and segmental ECVs of the left ventricle were measured by CT and MRI images. According to the location and pattern of delayed enhancement on MRI image, myocardial segments were classified into 3 groups: ischemic LGE segments (group 1), nonischemic LGE segments (group 2) and negative LGE segments (group 3). The correlation and agreement between CT-ECV and MRI-ECV were compared on a per-segment basis. Receiver operating characteristic (ROC) curve analysis was performed to establish a threshold for LIE detection. RESULTS: Among the 56 patients, 896 segments were analyzed, and of these, 73 segments were in group 1, 229 segments were in group 2, and 594 segments were in group 3. In segmental analysis, CT-ECV in group 3 (27.0%; 24.9–28.9%) was significantly lower than that in group 1 (33.2%; 30.7–36.3%) and group 2 (34.9%; 32.3–39.8%; all P

The members of the solute carrier (SLC) superfamily are vital membrane transporters in human cells. In the present study, we determine the expression and function of SLC5 family members in colorectal cancer (CRC). Expression analysis based on The Cancer Genome Atlas database and potential clinical relation analysis based on the Oncomine database indicate that SLC5A7 is downregulated and is predicted to correlate with the staging, and prognosis response of CRC. Additional results demonstrate that SLC5A7 is downregulated and correlates with good prognosis in patients with CRC. Ectopic expression of SLC5A7 either by overexpression, or uptake of choline efficiently inhibits CRC growth. Examination of the molecular mechanism reveals that SLC5A7 promotes p53 protein expression by directly interacting with and modifying p53 and disrupting the interaction between p53 and MDM2 in wild type p53 CRC cells. Our findings establish the clear correlation between SLC5A7 and tumour growth, providing a novel potential therapeutic target for CRC.

As a sustainable and eco-friendly technology, the benthic microbial fuel cell (BMFC) has been emerged as alternative and potential approach to recover electrical energy by microorganisms, but lower power density and poor long-term life hinder their practical application. Modification of anodic materials is an efficient strategy to solve this problem. Here, a conductive and biocompatible hydrogel electrode, polyaniline-polypyrole-CNTs-Fe3O4 (PANI-PPy-CNTs-Fe3O4) is prepared and applied as anode in a simulated BMFC. The maximum power density of the BMFC with PANI-PPy-CNTs-Fe3O4 hydrogel anode (5901.49 mW/m3) is 1.33, 2.15 and 2.06 times higher than that of PANI-PPy (4413.03 mW/m3), PANI and PPy anodes (2737.12 and 2859.53 mW/m3), respectively. The charge transfer resistance of quaternary hydrogel bioanode in BMFC (3.922 Ω) is much lower than that of the PANI (8.682 Ω), PPy (8.262 Ω) and PANI-PPy (5.772 Ω) hydrogel bioanodes. Moreover, the extracellular electron transfer ability is also enhanced on the composite hydrogel anode, which also exhibits the high biomass. High-throughput sequencing technology indicates that the synergistic effect of bacteria on the quaternary hydrogel made full use of organic matter as available fuel to enable a high electricity-generation anode. Such foregoing mainly ascribed to the composite hydrogel keep the high biocompatibility from components, while the addition of CNTs and Fe3O4 dramatically decreases the internal resistance and provides more electrochemical active surface area on basis of macroporous 3D hydrogel structure. This work explores the composite hydrogel used as anodes to construct high-performance BMFC and provides significant information for the applications of actual BMFCs in the future.

A porous carbon framework is successfully synthesized from lycium chinensis via a novel strategy using melamine matched with KOH as dual-activator. The biomass-derived carbon framework with hierarchical macro-/meso-/micro pores demonstrates an ultrahigh surface area of 3344 m2 g−1 and a sufficient total pore volume of 1.71 cm3 g−1. The porous carbon electrode with optimized structure presents an outstanding electrochemical performance. The specific capacitance reaches 520.0 F g−1 at 1 A g−1 and 291.0 F g−1 at 30 A g−1 with 96.8 % capacitance retention after 10 000 cycles at 30 A g−1. The energy density is also as high as 12.5 W h kg−1 for the electrode. The relationship between optimized structure and excellent performance of carbon materials is deeply explored. The superior electrochemical performance of carbon framework can be ascribed to its hierarchical porosity, ultrahigh surface area, sufficient total pore volume, proper graphitization degree and favorable heteroatom-doping, which will result in the fast ion diffusion, sufficient charge storage as well as the contributed pseudocapacitance. The work provides an effective guidance for synthesizing the superb porous biomass-derived carbon materials for supercapacitor with high performance.

Methods to detect and quantify disease biomarkers with high specificity and sensitivity in biological fluids play a key role in enabling clinical diagnosis, including point-of-care testing. Myeloperoxidase (MPO) is an emerging biomarker for the detection of inflammation, neurodegenerative diseases, and cardiovascular disease, where excess MPO can lead to oxidative damage to biomolecules in homeostatic systems. While numerous methods have been developed for MPO analysis, most techniques are challenging in clinical applications due to the lack of amplification methods, high cost, or other practical drawbacks. Enzyme-linked immunosorbent assays are currently used for the quantification of MPO in clinical practice, which is often limited by the availability of antibodies with high affinity and specificity and the significant nonspecific binding of antibodies to the analytical surface. In contrast, nucleic acid-based biosensors are of interest because of their simplicity, fast response time, low cost, high sensitivity, and low background signal, but detection targets are limited to nucleic acids and non-nucleic acid biomarkers are rare. Recent studies reveal that the modification of a genome in the form of phosphorothioate is specifically sensitive to the oxidative effects of the MPO/H2O2/Cl- system. We developed an oxidative cleavage-based three-dimensional DNA biosensor for rapid, ratiometric detection of HOCl and MPO in a "one-pot" method, which is simple, stable, sensitive, specific, and time-saving and does not require a complex reaction process, such as PCR and enzyme involvement. The constructed biosensor has also been successfully used for MPO detection in complex samples. This strategy is therefore of great value in disease diagnosis and biomedical research.

Ripening of fleshy fruits involves both diverse post-translational modifications (PTMs) and dynamic transcriptional reprogramming, but the interconnection between PTMs, such as protein phosphorylation and transcriptional regulation, in fruit ripening remains to be deciphered. Here, we conducted a phosphoproteomic analysis during banana (Musa acuminata) ripening and identified 63 unique phosphopeptides corresponding to 49 proteins. Among them, a Musa acuminata basic leucine zipper transcription factor21 (MabZIP21) displayed elevated phosphorylation level in the ripening stage. MabZIP21 transcript and phosphorylation abundance increased during banana ripening. Genome-wide MabZIP21 DNA binding assays revealed MabZIP21-regulated functional genes contributing to banana ripening, and electrophoretic mobility shift assay, chromatin immunoprecipitation coupled with quantitative polymerase chain reaction, and dual-luciferase reporter analyses demonstrated that MabZIP21 stimulates the transcription of a subset of ripening-related genes via directly binding to their promoters. Moreover, MabZIP21 can be phosphorylated by MaMPK6-3, which plays a role in banana ripening, and T318 and S436 are important phosphorylation sites. Protein phosphorylation enhanced MabZIP21-mediated transcriptional activation ability, and transient overexpression of the phosphomimetic form of MabZIP21 accelerated banana fruit ripening. Additionally, MabZIP21 enlarges its role in transcriptional regulation by activating the transcription of both MaMPK6-3 and itself. Taken together, this study reveals an important machinery of protein phosphorylation in banana fruit ripening in which MabZIP21 is a component of the complex phosphorylation pathway linking the upstream signal mediated by MaMPK6-3 with transcriptional controlling of a subset of ripening-associated genes.

Effects of manganese (Mn) toxicity stress on the growth of soybean, the number of Mn spots on leaves and the absorption of iron and magnesium were studied by nutrient solution hydroponics. The results showed that the presence of Mn spots on leaves was the main symptom of Mn toxicity in soybean. When the concentration of exogenous Mn was 25 μmol/l, the leaf generated obvious Mn oxidation spots; when the concentration of exogenous Mn exceeded 50 μmol/l, the growth of soybean was inhibited, and the number of Mn spots increased significantly. With the increase in exogenous Mn concentration, the Mn concentration in the roots, young leaves and old leaves of soybean increased significantly. When the concentration of exogenous Mn reached 200 μmol/l, the number of Mn spots on primary leaves, old leaves and young leaves increased significantly. Although the iron concentration in the roots remained the same, the iron content in the old and young leaves decreased significantly. On the other hand, although Mn toxicity significantly reduced the concentration of magnesium in soybean roots, it increased the concentration of magnesium in old and young leaves. Bangladesh J. Bot. 50(3): 803-811, 2021 (September) Special

Constructing highly efficient and durable non-noble metal modified carbon catalysts for oxygen reduction reaction (ORR) in the whole pH range is essential for energy conversion devices but still remains a challenge. Herein, the Fe/Fe3C nanoparticles and Fe-NX species anchored on the interconnected mesoporous carbon materials are fabricated through an economical and facile template-assisted polymerization-pyrolysis strategy. The catalyst exhibits unique features with the electronic interaction between Fe/Fe3C and Fe−NX, large specific surface area and high mesoporous structure as well as nitrogen doping in porous carbon skeletons, which can effectively catalyze ORR over the full pH range. In an alkaline electrolyte, the optimized catalyst displays favorable ORR performance with positive onset potential (Eonset = 0.91 V), half-wave potential (E1/2 = 0.83 V), long-term cycles stability and methanol tolerance, exceeding those for the commercial Pt/C. Furthermore, the prepared catalyst could be directly assembled into the alkaline Zn−air battery that exhibits the open-circuit voltage of 1.44 V, high power density of 96.0 mW cm−2 and long-term durability. Therefore, the template-assisted polymerization-pyrolysis strategy provides a promising route for designing high-performance non-noble metal decorated ORR electrocatalysts.

A free-standing MoS2–graphene flexible film (MoS2/GN-F) is designed and prepared by a facile vacuum filtration method without using any templates. SEM and TEM images show that the MoS2/GN flower-like particles are self-assembled by MoS2 nanoflakes and graphene nanosheets. Electrochemical performances of the MoS2/GN-F film as anode active material in Lithium-ion batteries (LIBs) are investigated in both MoS2/GN//Li half-cells and MoS2/GN//LiCoO2 full-cells. The MoS2/GN-F sample maintains high reversible discharge capacities of 700.3 mAh g−1 after 100 cycles at 400 mA g−1 in MoS2/GN//Li half-cells. The assembled MoS2/GN-F//LiCoO2 full-cell delivers high initial discharge capacities of 1149.1 mAh g−1. The excellent lithium storage performances of the obtained MoS2/GN-F film can be mainly attributed to the designed novel structure of the composite. The cross-linked graphene nanosheets, the anchoring MoS2 nanoflakes, and the synergistic effects between them make the composite good conductivity, enough buffering space for the volume change, and shortened ionic transport length. This work clearly demonstrates that the MoS2/GN-F film is a promising alternative material for anode in the LIB applications.

Oleanolic acid (OA) is a triterpenoid commonly found in plants and has shown extensive pharmaceutical activities. This study aimed to investigate the underlying mechanism of antiosteoporosis (OP) action of OA by utilizing the network pharmacology approach and molecular docking methods. First, the targets of OA were identified using the GeneCards, Stitch, and Swisstarget databases, and the targets related to OP were mined using the NCBI, Genecards, and DisGeNet databases. The overlapped targets of OA and OP were regarded as candidate targets, and the String database was used to obtain the protein–protein interactions among the targets. Then, Gene Ontology (GO) functional enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) metabolic pathway enrichment pathways of the candidate targets were performed using the DAVID database. In addition, the top 16 targets in the protein interaction network were used for molecular docking. Finally, an animal model constructed using d-galactose-induced oxidative stress and a low-calcium diet with accelerated bone loss was used to verify the in vivo effects of OA on osteoporotic mice. A total of 42 candidate targets for OA to treat OP were obtained. According to the protein–protein interaction network, MAPK1 showed the highest connectivity with other proteins. Additionally, GO analysis identified the top 20 biological processes, 9 cellular components, and top 20 molecular functions. Moreover, the candidate targets were mainly involved in 13 signaling pathways such as TNF signaling pathway, insulin resistance, MAPK signaling pathway, apoptosis, and PI3K-Akt signaling pathways. Furthermore, molecular docking revealed that OA has a high degree of connections with 16 key proteins. In addition, the anti-OP effects of OA are further validated through the in vivo model. Altogether, our study elucidated the candidate targets for OA to alleviate OP, explored the protein–protein interactions and related signaling pathways of the targets, and validated the anti-OP effects of OA. It could provide a better understanding of the action mechanism in OA to treat OP.

Metal-organic cages, a class of supramolecular containers constructed by the self-assembly of metal ions and organic ligands, show great promise as catalytic agents. In this work, we designed and synthesized a series of rhombic dodecahedral Ni-Cu heterometal imidazolate cages (Ni8Cu6L24) that can act as highly active photo-Fenton-like catalysts. These cages possess a high ability to generate hydroxyl radicals (•OH) under visible light in the presence of H2O2, which can rapidly degrade organic pollutants (e.g., rhodamine B, methylene blue, and methyl orange) into CO2 and H2O. Besides, they are robust catalysts, with high catalytic activity and reusability under conditions in high H2O2 concentration, providing potentially advanced materials for degrading persistent organic pollutants.

Sepsis is the leading cause of death in hospital intensive care units. In light of recent studies showing that variations in N6-methyladenosine (m6A) levels in different RNA transcripts influence inflammatory responses, we evaluated the m6A profiles of rat aortic mRNAs and lncRNAs after lipopolysaccharide (LPS)-induced sepsis. LC-MS-based mRNA modification analysis showed that global m6A levels were significantly decreased in aortic tissue of rats injected intraperitoneally with LPS. This finding was consistent with downregulated expression of METTL3 and WTAP, two members of the m6A writer complex, in LPS-exposed aortas. Microarray analysis of m6A methylation indicated that 40 transcripts (31 mRNAs and 9 lncRNAs) were hypermethylated, while 223 transcripts (156 mRNAs and 67 lncRNAs) were hypomethylated, in aortic tissue from LPS-treated rats. On GO and KEGG analyses, 'complement and coagulation cascades', 'transient receptor potential channels', and 'organic anion transmembrane transporter activity' were the major biological processes modulated by the differentially m6A methylated mRNAs. In turn, competing endogenous RNA network analysis suggested that decreased m6A levels in lncRNA-XR_343955 may affect the inflammatory response through the cell adhesion molecule pathway. Our data suggest that therapeutic modulation of the cellular m6A machinery may be useful to preserve vascular integrity and function during sepsis.

BACKGROUND AND PURPOSE Endothelium-derived hyperpolarizing factor (EDHF) has been suggested as a therapeutic target for vascular protection against ischaemic brain injury. However, the molecular entity of EDHF and its action on neurons remains unclear. This study was undertaken to demonstrate whether the hydrogen sulfide (H2 S) acts as EDHF and exerts neuroprotective effect via large-conductance Ca2+ -activated K+ (BKCa /KCa 1.1) channels. EXPERIMENTAL APPROACH The whole-cell patch-clamp technology was used to record the changes of BKCa currents in rat neurons induced by EDHF. The cerebral ischaemia/reperfusion model of mice and oxygen-glucose deprivation/reoxygenation (OGD/R) model of neurons were used to explore the neuroprotection of EDHF by activating BKCa channels in these neurons. KEY RESULTS Increases of BKCa currents and membrane hyperpolarization in hippocampal neurons induced by EDHF could be markedly inhibited by BKCa channel inhibitor iberiotoxin or endothelial H2 S synthase inhibitor propargylglycine. The H2 S donor, NaHS-induced BKCa current and membrane hyperpolarization in neurons were also inhibited by iberiotoxin, suggesting that H2 S acts as EDHF and activates the neuronal BKCa channels. Besides, we found that the protective effect of endothelium-derived H2 S against mice cerebral ischaemia/reperfusion injury was disrupted by iberiotoxin. Importantly, the inhibitory effect of NaHS or BKCa channel opener on OGD/R-induced neuron injury and the increment of intracellular Ca2+ level could be inhibited by iberiotoxin but enhanced by co-application with L-type but not T-type calcium channel inhibitor. CONCLUSION AND IMPLICATIONS Endothelium-derived H2 S acts as EDHF and exerts neuroprotective effects via activating the BKCa channels and then inhibiting the T-type calcium channels in hippocampal neurons.

Steady-state absorption, emission, and time-resolved spectroscopy were utilized to study the dynamics of excited states of linear and multi-branched bithiazole derivatives in different solvents at room temperature. In the studied compounds, triphenylamine and bithiazole groups act as donor and acceptor, respectively. BTZ-I and II have similar linear molecular structures, while BTZ-III and BTZ-IV have multi-branched structures. The difference is that the donor and acceptor units are connected by a single bond or a triple bond, respectively. With increase in solvent polarity, the fluorescence spectra exhibit a red shift and the fluorescence lifetime increases. Our results suggest there is intra-molecular charge transfer (ICT) processes in these four samples.

Carbohydrates play essential roles in a variety of biological processes that are dictated by their structures. However, characterization of carbohydrate structures remains extremely difficult and generally unsolved. In this work, a de novo mass spectrometry-based workflow was developed to isolate and structurally elucidate oligosaccharides to provide sequence, monosaccharide compositions, and glycosidic linkage positions. The approach employs liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based methods in a 3-dimensional concept: one high performance liquid chromatography-quadrupole time-of-flight mass spectrometry (HPLC-QTOF MS) analysis for oligosaccharide sequencing and two ultra high performance liquid chromatography-triple quadrupole mass spectrometry (UHPLC-QqQ MS) analyses on fractionated oligosaccharides to determine their monosaccharides and linkages compositions. The workflow was validated by applying the procedure to maltooligosaccharide standards. The approach was then used to determine the structures of oligosaccharides derived from polysaccharide standards and whole food products. The integrated LC-MS workflow will reveal the in-depth structures of oligosaccharides.

Early cancer diagnosis requires ultrasensitive detection of tumor markers in blood. To this end, we develop a novel microcantilever immunosensor using nanobodies (Nbs) as receptors. As the smallest antibody (Ab) entity comprising an intact antigen-binding site, Nbs achieve dense receptor layers and short distances between antigen-binding regions and sensor surfaces, which significantly elevate the generation and transmission of surface stress. Owing to the inherent thiol group at the C-terminus, Nbs are covalently immobilized on microcantilever surfaces in directed orientation via one-step reaction, which further enhances the stress generation. For microcantilever-based nanomechanical sensor, these advantages dramatically increase the sensor sensitivity. Thus, Nb-functionalized microcantilevers can detect picomolar concentrations of tumor markers with three orders of magnitude higher sensitivity, when compared with conventional Ab-functionalized microcantilevers. This proof-of-concept study demonstrates an ultrasensitive, label-free, rapid, and low-cost method for tumor marker detection. Moreover, interestingly, we find Nb inactivation on sensor interfaces when using macromolecule blocking reagents. The adsorption-induced inactivation is presumably caused by the change of interfacial properties, due to binding site occlusion upon complex coimmobilization formations. Our findings are generalized to any coimmobilization methodology for Nbs and, thus, for the construction of high-performance immuno-surfaces. Electronic Supplementary Material Supplementary material (experimental section, HER2 detection using anti-HER2-mAb-functionalized microcantilevers) is available in the online version of this article at 10.1007/s12274-021-3588-4.

Water oxidation to molecular oxygen is indispensable but a challenge for splitting H2O. In this work, a series of Co-based metal-organic cages (MOCs) for photoinduced water oxidation were prepared. MOC-1 with both bis(μ-oxo) bridged dicobalt and Co-O (O from H2O) displays catalytic activity with an initial oxygen evolution rate of 80.4 mmol/g/h and a TOF of 7.49 × 10-3 s-1 in 10 min. In contrast, MOC-2 containing only Co-O (O from H2O) in the structure results in a lower oxygen evolution rate (40.8 mmol/g/h, 4.78 × 10-3 s-1), while the amount of oxygen evolved from the solution of MOC-4 without both active sites is undetectable. Isotope experiments with or without H218O as the reactant successfully demonstrate that the molecular oxygen was produced from water oxidation. Photophysical and electrochemical studies reveal that photoinduced water oxidation initializes via electron transfer from the excited [Ru(bpy)3]2+* to Na2S2O8, and then, the cobalt active sites further donate electrons to the oxidized [Ru(bpy)3]3+ to drive water oxidation. This proof-of-concept study indicates that MOCs can work as potential efficient catalysts for photoinduced water oxidation.

Inhibition of RhoA-ROCK pathway is involved in the H2S-induced cerebral vasodilatation and H2S-mediated protection on endothelial cells against oxygen-glucose deprivation/reoxygenation injury. However, the inhibitory mechanism of H2S on RhoA-ROCK pathway is still unclear. The aim of this study was to investigate the target and mechanism of H2S in inhibition of RhoA/ROCK. GST-RhoAwild and GST-RhoAS188A proteins were constructed and expressed, and were used for phosphorylation assay in vitro. Recombinant RhoAwild-pEGFP-N1 and RhoAS188A-pEGFP-N1 plasmids were constructed and transfected into primary hippocampal nerve cells (HNCs) to evaluate the neuroprotective mechanism of endothelial H2S by using transwell co-culture system with endothelial cells from cystathionine-γ-lyase knockout (CSE−/−) mice and 3-mercaptopyruvate sulfurtransferase knockout (3-MST−/−) rats, respectively. We found that NaHS, exogenous H2S donor, promoted RhoA phosphorylation at Ser188 in the presence of cGMP-dependent protein kinase 1 (PKG1) in vitro. Besides, both exogenous and endothelial H2S facilitated the RhoA phosphorylation at Ser188 in HNCs, which induced the reduction of RhoA activity and membrane transposition, as well as ROCK2 activity and expression. To further investigate the role of endothelial H2S on RhoA phosphorylation, we detected H2S release from ECs of CSE+/+ and CSE−/− mice, and 3-MST+/+ and 3-MST−/− rats, respectively, and found that H2S produced by ECs in the culture medium is mainly catalyzed by CSE synthase. Moreover, we revealed that both endothelial H2S, mainly catalyzed by CSE, and exogenous H2S protected the HNCs against hypoxia-reoxygenation injury via phosphorylating RhoA at Ser188.

The synthesis of poly(ethylene oxide) (PEO) with amino end group, a key functionality for PEGylation, is a long-standing challenge. Multistep routes based on postmodification or covalent protection have been adopted to circumvent ethoxylation of the amino group by ethylene oxide (EO). Here, we report a noncovalent protection strategy for one-step synthesis of PEO amine. An amino (di)alcohol is mixed with a small amount of mild phosphazene base and excess triethylborane (Et

Purpose: The purpose of this study is to develop a new PLGA based formulation for microspheres, which aims to release mometasone furoate for one month, so as to improve compliance. Methods: The microspheres containing mometasone furoate were prepared by oil in water emulsion and solvent evaporation. The microspheres were characterized by surface morphology, shape, size and encapsulation efficiency. The release in vitro was studied in 37°C phosphate buffer, and in vivo, pharmacodynamics and preliminary safety evaluation were conducted in male Sprague Dawley rats. Results: The morphology results showed that the microspheres have a smooth surface, spherical shape and an average diameter of 2.320-5.679μm. The encapsulation efficiency of the microspheres loaded with mometasone furoate was in the range of 53.1% to 95.2%, and the encapsulation efficiency of the microspheres could be greatly affected by the proportion of oil phase to the water phase and other formulation parameters. In vitro release kinetics revealed that drug release from microspheres was through non-Fick's diffusion and PLGA polymer erosion. Pharmacokinetic data showed that the initial release of microspheres was small and then sustained. The results of the pharmacodynamics study fully proved the long-term effectiveness of mometasone furoate microspheres. The results of in vivo safety evaluation showed that the preparation system possessed good in vivo safety. Conclusion: This study shows that the microspheres prepared in this study have sufficient ability to stable drug release at least for 35 days, with good efficacy and high safety. In addition, mometasone furoate can be used as a potential candidate drug for 35 days long-term injection.

Methanotrophs in marine sediments and overlying water attenuate the emissions of methane into the atmosphere and thus play an important role for the global cycle of this greenhouse gas. However, gas released from natural hydrocarbon seeps are not pure methane but commonly mixed hydrocarbons. Currently, how methanotrophic bacteria behave in the co-presence of methane and heavier hydrocarbons remains unknown. In this paper, the bacteria were cultured aerobically in fresh sediment samples (collected from Bohai Bay in eastern China) at 28°C under the atmospheres of pure methane and methane+ethane+propane mixed gas, respectively. The prevailing terrigenous n-alkanes and fatty acids in the original sediment samples varied consistently after incubations, confirming the proceeding of aerobic bacterial activities. The real-time quantitative PCR assay and sequencing of the 16S rRNA and particulate methane monooxygenase (pmoA) genes revealed the changes of microbe communities to a methanotroph-dominating structure after incubations. Particularly, after incubations the family Methylococcaceae (type I methanotrophs) became dominant with proportions higher than 40%, whereas Methylocystaceae (type II methanotrophs) nearly disappeared in all incubated samples. Moreover, the species of methanotrophs from the samples treated with pure methane were dominated by Methylobacter luteus, whereas Methylobacter whittenburyi took the predominant proportion in the samples treated with mixed gas. The phenomenon suggests that some methanotrophs may also utilize ethane and propane. Collectively, this study may help to gain a better understanding of the effects and contributions of microbial activities in marine hydrocarbon seep ecosystems.

Background Thiophanate-methyl and its metabolite carbendazim are broad-spectrum fungicides used on many crops. The residues of these chemicals could result in potential environmental and human health problems. Therefore, investigations of the dissipation and residue behaviors of thiophanate-methyl and its metabolite carbendazim on cowpeas and associated dietary risk assessments are essential for the safety of agricultural products. Results A simple analytical approach using liquid chromatography with tandem mass spectrometry was developed and validated for the determination of thiophanate-methyl and carbendazim concentrations in cowpeas. Good linearity (R2 > 0.998) was obtained, and the recoveries and relative standard deviations were 80.0%-104.7% and 1.4%-5.2%, respectively. The dissipation rates of thiophanate-methyl, carbendazim and total carbendazim were high (half-lives of 1.61-2.46 days) and varied in the field cowpea samples because of the different weather conditions and planting patterns. Based on the definition of thiophanate-methyl, the terminal residues of total carbendazim in cowpea samples were below the maximum residue limits set by Japan for other legumes. The acute and chronic risk quotients of three analytes were 0.0%-27.6% in cowpea samples gathered from all terminal residue treatments, which were below 100%. Conclusion An optimized approach for detecting thiophanate-methyl and carbendazim in cowpeas was applied for the investigation of field-trial samples. The potential acute and chronic dietary risks of thiophanate-methyl, carbendazim and total carbendazim to the health of Chinese consumers were low. These results could guide the safe and proper use of thiophanate-methyl in cowpeas and offer data for the dietary risk assessment of thiophanate-methyl in cowpeas. This article is protected by copyright. All rights reserved.

The consequences of blast-induced traumatic brain injury (bTBI) on the blood–brain barrier (BBB) and components of the neurovascular unit are an area of active research. In this study we assessed the time course of BBB integrity in anesthetized rats exposed to a single blast overpressure of 130 kPa (18.9 PSI). BBB permeability was measured in vivo via intravital microscopy by imaging extravasation of fluorescently labeled tracers (40 kDa and 70 kDa molecular weight) through the pial microvasculature into brain parenchyma at 2–3 h, 1, 3, 14, or 28 days after the blast exposure. BBB structural changes were assessed by immunostaining and molecular assays. At 2–3 h and 1 day after blast exposure, significant increases in the extravasation of the 40 kDa but not the 70 kDa tracers were observed, along with differential reductions in the expression of tight junction proteins (occludin, claudin-5, zona occluden-1) and increase in the levels of the astrocytic water channel protein, AQP-4, and matrix metalloprotease, MMP-9. Nearly all of these measures were normalized by day 3 and maintained up to 28 days post exposure. These data demonstrate that blast-induced changes in BBB permeability are closely coupled to structural and functional components of the BBB.

The new generation of electronics tends to be well-performed, facile and environmentally friendly. Here, we report a bio-assembled sensitive pressure senor based on reduced graphene oxide-bacterial cellulose/bacterial cellulose (RGO-BC/BC) bilayer films, integrated by bacteria in one step. The advantage of this integration is that there is strong nanofiber connection between the conductive RGO-BC and insulative highly compressible porous BC layer, which confers RGO-BC/BC film electrode with good robustness, tailorability, flexibility and wearability. Without extra bonding-interface or postprocessing, the RGO-BC/BC bilayer films could be directly assembled into pressure sensing devices. Ascribed from the good reversible compressibility of the BC layer and incorporated bilayer structure, the pressure sensor performs good sensitivity and excellent durability and bending stability. The facile sensitive capacitive sensor could monitor the human hand or finger motion in real time. The sensing array is able to detect the spatial distribution of pressure mounted in the flat plane as well as curved surface of human body, succeeding in the correction of human walking posture for health care. The e-skins are potential in wearable electronics, artificial intelligence, soft robots, healthcare etc.

Flumioxan was used to control annual broad-leaved and dicotyledonous weeds. Considering the limited information available, comprehensive investigation of persistence and mobility of flumioxazin in Chinese soil is very important. The degradation, adsorption-desorption, mobility, and leaching risk of flumioxazin in four Chinese soils were investigated under laboratory conditions. The degradation rates of flumioxazin, which correlated with soil moisture, microorganisms, organic matter and pH, were 8.2−50.6 days in the four soils under different conditions. Microorganisms influenced these rates greatly, with half-lives increasing 1.67−2.39-fold. Three possible metabolites were detected by ultrahigh-performance liquid chromatography with high-resolution mass spectrometry, and the metabolic pathways were cleavage of the imide and amide linkages and opening of the cyclic imide. The adsorption capacity of flumioxazin in soil was strongly positively correlated with the soil’s cation exchange capacity (CEC) and organic matter (OM) content, which had correlation coefficients > 0.83. Negative and positive desorption hysteresis effects were observed in Guizhou soil and the other three soils, respectively, which might be related to the different soil constitutions. The mobility was relatively weak in the four Chinese soils and negatively related to CEC and OM content, with correlation coefficients > 0.86. Moreover, the leaching risk of flumioxazin was uncertain for the underground water. The results indicated that flumioxazin was a low-risk herbicide and could be used to evaluate the environmental fate and risk of flumioxazin in soil.

Excellent crystallinity and uniform composition distribution of the Cu2ZnSn(S,Se)4 (CZTSSe) absorber are indispensable factors for the fabrication of photovoltaic device with excellent performance. Here, a facile and effective method is developed to improve the composition uniformity of CZTSSe absorber. It is inspiring that by replacing the acetates with chlorides as the solutes in the precursor solution, the issue of the composition non-uniformity especially for the distribution of Cu and Sn, which is ascribed to the rich-carbon in the acetate-based CZTSSe absorber, is able to be avoided. Due to less organic residues and composition uniformity, the grain size and the crystallinity of absorber could be significantly enhanced, and the photovoltaic performance of chloride-based CZTSSe solar cell is improved remarkably. Furthermore, substituting CuCl2 with CuCl as the copper source in the precursor solution is able to obtain a stable solution, and the quality of CZTSSe absorber is further improved. As a consequence, 8.48% efficient CZTSSe solar cell has been yield.

An increasing number of studies have shown that Faecalibacterium prausnitzii (F. prausnitzii) is a promising anti-inflammatory bacterium that colonizes in the gut and that gut microbiota dysbiosis plays an important role in the pathogenesis of inflammatory bowel disease (IBD). In this study, we report the gut microbiota profile of 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis mice treated with F. prausnitzii and its supernatant on the basis of high-throughput sequencing. We interestingly found that both F. prausnitzii and its metabolites exerted protective effects against colitis in mice, which ameliorated gut dysbiosis, with an increase in bacterial diversity and the abundance of short-chain fatty acid (SCFA)-producing bacteria and a decrease in serum TNF-α and the abundance of Proteinbacteria, Acidobacteria, and Bacteroidetes. These findings will provide further evidence of the anti-inflammatory effect of F. prausnitzii, which presents therapeutic potential for IBD treatment.

Reverse osmosis (RO) membrane technology, as an effective and eco-friendly method, has been widely used for seawater desalination and sewage treatment. However, RO membranes inevitably suffer serious organic and biological fouling during operation. Herein, we fabricated a hydrophilic anti-fouling layer on the RO membrane surface through the synergistic effect of covalent bonds and coordination bonds. Polyethyleneimine (PEI) and polyaspartic acid (PASP) are assembled onto the RO membrane surface successively. Fe(III) is utilized to induce further cross-linking for fabricating the PEI/PASP/Fe layer. The modified membranes exhibit superior hydrophilicity, whose water contact angle declines from 86.7° to 23.6°. In addition, the water flux of the PEI/PASP/Fe membrane increases by 45.8% with an excellent desalting property. Long-term, multi-cycle membrane fouling experiments demonstrate that the modified membrane manifests not only a lower flux loss rate (DRt) but also a higher flux recovery rate (FRR). This means that the hydrophilic layer modified membranes show excellent separation performance even under severe environments, which is expected to boost the anti-fouling research in the membrane field.