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The "active site isolation" strategy has been proved to be efficient for enhancing the catalytic performance in propane dehydrogenation (PDH). Herein, spatially isolated cobalt oxide sites within nitrogen-doped carbon (NC) layers supported on silicalite-1 zeolite (CoOx@NC/S-1) were synthesized by a two-step process consisting of the pyrolysis of bimetallic Zn/Co zeolitic imidazole frameworks loaded on silicalite-1 (ZnCo-ZIF/S-1) under N2 and the subsequent calcination in air atmosphere. This catalyst possesses exceptional catalytic performance for PDH with the propane conversion of 40% and the propene selectivity of >97%, and no apparent deactivation is observed after 10 h PDH reaction at 600 °C. https://www.selleckchem.com/products/sb-3ct.html With intensive characterizations and experiments, it is indicated that the real active sites of CoOx@NC/S-1 are isolated CoO sites during the PDH process. In situ FT-IR spectroscopy shows the same intermediate product (Co-C3H7) during both propane dehydrogenation and propene hydrogenation, indicating that they have a reverse reaction process, and a reaction mechanism for PDH is proposed accordingly. The properties of stable gold (Au) nanoparticle dispersions can be tuned to alter their activity towards biomembrane models. Au nanoparticle coating techniques together with rapid electrochemical screens of a phospholipid layer on fabricated mercury (Hg) on platinum (Pt) electrode have been used to moderate the phospholipid layer activity of Au nanoparticle dispersions. Screening results for Au nanoparticle dispersions were intercalibrated with phospholipid large unilamellar vesicle (LUV) interactions using a carboxyfluorescein (CF) leakage assay. All nanoparticle dispersions were characterised for size, by dynamic light scattering (DLS) and transmission electron microscopy (TEM). Commercial and high quality home synthesised Au nanoparticle dispersions are phospholipid monolayer active whereas Ag nanoparticle dispersions are not. If Au nanoparticles are coated with a thin layer of Ag then the particle/lipid interaction is suppressed. The electrochemical assays of the lipid layer activity of Au nanopartiered saline (PBS) solutions removes their phospholipid layer interaction. Inconsistent findings have been reported on the link between dietary carbohydrates and lung cancer. This study aims to comprehensively evaluate the role of dietary carbohydrates on lung cancer risk. The prospective study is based on the PLCO trial, which recruited 113,096 eligible participants across the United States. Participants had to have completed baseline and diet history questionnaires. The incidence of lung cancer was acquired through self-report and medical record follow-up. A multivariable logistic model adjusted for confounders was used to estimate odds ratios (ORs) and 95 % confidence intervals (CIs) of dietary carbohydrates, fiber, whole grains, glycemic index (GI) and glycemic load (GL) for lung cancer. Similar methods were applied in analyzing the carbohydrates and fiber from different food sources. Multinomial logistic models were used for sensitivity analysis with lung cancer subtypes as outcomes. Dietary carbohydrates and GL were inversely associated with lung cancer incidence in the PLCO population. Among various carbohydrates, 30-g daily consumption of dietary fiber was related to a lower risk of lung cancer (fourth vs first quartile OR 0.62, 95 % CI 0.54-0.72) compared with 8.8-g. Furthermore, consuming whole grains 2.3 servings per day as opposed to 0.3 servings per day was associated with a lower risk of lung cancer (OR 0.73, 95 % CI 0.64-0.83). A higher risk of lung cancer was seen for the consumption of high-GI food (OR 1.19, 95 % CI 1.05-1.35) and refined carbohydrates from soft drinks (OR 1.23, 95 % CI 1.04-1.46). Carbohydrates and fiber from fruits, vegetables and whole grains are associated with lower lung cancer risk. Refined carbohydrates from processed food, such as soft drinks, appear to increase risk. Carbohydrates and fiber from fruits, vegetables and whole grains are associated with lower lung cancer risk. Refined carbohydrates from processed food, such as soft drinks, appear to increase risk.A reverse micelle mediated dispersive liquid-liquid microextraction (RM-DLLME) combined with high performance liquid chromatography-ultraviolet detector (HPLC-UV) was developed for extraction and determination of 5 A2 components of teicoplanin (TA2-1, TA2-2, TA2-3, TA2-4, TA2-5) in human plasma, and the mechanism of RM-DLLME was analysed and explored. In this method, 80 µL of the reverse micelle solution of cetylpyridinium chloride/n-hexanol (15 mmol/L) was used as the extraction solvent for the separation, extraction and enrichment of the teicoplanin in plasma sample. All factors affecting the extraction efficiencies of the target analytes, such as the amounts of acetonitrile and chloroform, the type and volume of reverse micelle solution, pH and volume of sample phase, dispersant, salt addition, extraction mode and time, centrifugation rate and time, were investigated and optimized. Under the optimum conditions, the 5 A2 components of teicoplanin achieved effective enrichment with the enrichment factors of 228-347 and obtained good linearity in the range of 0.8375-100.5 µg/mL with correlation coefficients higher than 0.9960. The limits of detection were ranged between 0.5025-3.015 µg/mL. Relative standard deviation values of the method precisions were lower than 10.6% and the average recoveries were in the range of 82.7-111.3%. The determination results of the method were demonstrated with favorable characteristics, such as high enrichment, good selectivity and sensitivity, satisfactory precision and accuracy, and this method could be employed to analysis of the teicoplanin in human plasma samples.Copper ions (Cu2+) are key constituents of copper-based antimicrobial compounds (CBACs), which are extensively used in agriculture. Previously, we demonstrated that a low concentration of Cu2+ induced plant defenses associated with callose deposition in Arabidopsis as well as flg22, a microbe-associated molecular pattern (MAMP) peptide. However, the details and differences of the mechanisms between Cu2+- and flg22-mediated callose deposition remain unclear. Here, we reported that Cu2+- and flg22-induced defense responses and callose deposition are dependent on AtACS8 and AtACS2/AtACS6, respectively. After the RNA sequencing data were mined, the expression of MYB51, MYB122, CYP79B2/B3 and CYP83B1 implied that a conserved downstream indole glucosinolate (IGS) metabolic pathway is regulated by Cu2+. In the Cu2+-induced response, the ethylene biosynthesis rate-limiting gene AtACS8 and the signal transduction pathway were found to be required for Cu2+-activated MYB51 and MYB122 transcription. Functional redundancy of MYB51 and MYB122, the key regulators of the IGS metabolic pathway, was identified in the Cu2+-mediated regulation of IGS gene transcription, promotion of callose deposition, and increase in Arabidopsis resistance to bacterial pathogens.
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