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Catalysts · 2019 ·Vol. 9 ·期 8 ·672 · IF 3.444

Synthesis of Hierarchical Titanium Silicalite-1 Using a Carbon-Silica-Titania Composite from Xerogel Mild Carbonization

Xinya Pei,Xiaoxue Liu,Xiaoyu Liu,Jinling Shan,Hui Fu,Ying Xie,Xuemin Yan,Xianzhu Meng,Yancheng Zheng,Geng Li,Qi Wang,Hao Li

Hierarchical titanium silicalite-1 (HTS-1) zeolites are an important class of catalytic materials due to their enhanced mass transfer and improved catalytic performance. In this study, HTS-1 zeolites have been successfully prepared by the hydrothermal crystallization of carbon-silica-titania (CST) composites. Compared with the direct carbonization method, the mild carbonization of SiO2-TiO2/Tween 40 xerogel in the presence of sulfuric acid can effectively improve both the content and mesoporous structure of carbon material in the CST composites, which enables carbon materials to better play the role of a mesoporous template during the crystallization process. The resultant zeolite has both ordered micropores and interconnected mesopores and macropores, which are similar to the skeleton of the carbon template trapped in the TS–1 crystals. Moreover, the HTS–1 zeolite displays outstanding catalytic performance in oxidative desulfurization of bulky sulfur compounds.

研究领域: 材料科学 · 催化化学 · 纳米多孔材料 · 环境催化 · 能源化工
✓ 已验证 DOI 高影响因子
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EUROPEAN JOURNAL OF MEDICAL RESEARCH · 2024 · IF 2.8

Baicalin promotes the sensitivity of NSCLC to cisplatin by regulating ferritinophagy and macrophage immunity through the KEAP1-NRF2/HO-1 pathway

Yang Chen,Shujun Bao,Zhongzhao Wang,Zheng Fang,Hao Tang

Background Cisplatin (DDP) chemotherapy is commonly used in therapy for non-small cell lung cancer (NSCLC), but increased drug resistance has become a huge obstacle. Baicalin (BA) contributed to the sensitivity of NSCLC to DDP. Here, we aimed to further probe the pathophysiological mechanisms of BA in NSCLC. Methods A549 and A549/DDP cells and xenograft mice were treated with BA and DDP. Xenograft mice were treated additionally with the NRF2 inducer (Bardoxolone methyl, BM) and KEAP1 knockdown. The levels of ferritinophagy-related proteins and biomarkers were determined. The autophagosomes were observed. M1 macrophage polarization and the contents of related indicators were analyzed. The involvement of KEAP1/NRF2/HO-1 was determined. Results BA inhibited cell development, and the effect of BA and DDP on cell development was additive. The abundance of ferritinophagy-related proteins and the number of autophagosomes were induced by BA. BA also promoted the transition of GSH to GSSH. BA favored M1 macrophage polarization and affected the expression of related proteins. When BA and DDP combined, these molecular phenomena were further exacerbated. BA induced accumulation of KEAP1 and reduction of NRF2 and HO-1. However, BM and KEAP1 knockdown disrupted the synergistic effects of BA and DDP on inhibiting NSCLC growth. BM and KEAP1 knockdown reversed DDP and BA-promoted protein expression activity and M1 macrophage polarization. Conclusion Our findings suggest that BA is involved in ferritinophagy and macrophage immunity through the KEAP1-NRF2/HO-1 axis, thereby improving the DDP sensitivity in NSCLC, which could provide new candidates for treatment strategies.

研究领域: 肿瘤学 · 药理学 · 免疫学 · 分子生物学
✓ 已验证 DOI PubMed 高影响因子
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CHEMOSPHERE · 2020 · IF 5.778

Transformation of sulfadiazine in humic acid and polystyrene microplastics solution by horseradish peroxidase coupled with 1-hydroxybenzotriazole

Yifei Leng,Henglin Xiao,Zhu Li,Ying Liu,Jun Wang

Enzyme catalyzed coupling with redox mediators are considered as great interesting and viable technologies to transform antibiotics. This work demonstrated the horseradish peroxidase (HRP) was effective in transforming sulfadiazine (SDZ) transformation coupled with 1-hydroxybenzotriazole (HBT) at varying conditions. The removal of SDZ was independent of Na + and its ionic strength, but Ca 2+ could enhance transformation efficiency by increasing the enzyme activity of HRP. The presence of humic acid (HA) and polystyrene (PS) microplastics showed inhibition on the transformation of SDZ, and the transformation rate constants ( k ) decreased with the concentration of HA and PS particles increased. These primarily attributed to covalent coupling and electrostatic interaction between SDZ and HA, SDZ and PS, respectively, which reduced the concentration of free SDZ in the reaction solution. The presence of cation recovered the inhibition of SDZ transformation by HA and PS particles, which ascribed to compete between cation and SDZ. The divalent cations (Ca 2+ ) showed more substantial competitiveness than mono (Na + ) due to more carried charge. Eight possible transformation products were identified, and potential SDZ transformation pathways were proposed, which include δ-cleavage, γ-cleavage, carbonylation, hydroxylation, SO 2 extrusion and SO 3 extrusion. In addition, HA and PS particles couldn’t affect the transformation pathways of SDZ. These findings provide novel understandings of the transformation and the fate of antibiotics in the natural environment by HRP coupled with redox mediators.

研究领域: 环境科学 · 生物化学
✓ 已验证 DOI 高影响因子
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2025 · IF 3.9

Direct Jet Fuel Synthesis Over Co/M-TUD-1 Catalysts by the Integration of Mesopore Confinement Effects and Acid Hydrocracking

Jing Bai,Wencheng Chen,Freeman Bwalya Kabwe,Xutao Shang,Guozhen Lin,Qian Jiang,Chenguang Wang

Amid growing global energy demands and the imperative to reduce carbon emissions, sustainable aviation fuel (SAF) production via Fischer–Tropsch (FT) synthesis has emerged as a pivotal solution. This study focuses on enhancing the selectivity of C8–C16 hydrocarbons for jet fuel through the integration of mesopore confinement effects and acid hydrocracking by developing novel Co/M-TUD-1 catalysts with a uniform, continuous three-dimensional mesoporous architecture. Utilizing sol–gel and melt infiltration methods for catalyst preparation and incorporating metals such as Al, Zr, La, and Ce, we explored how different supports influence FT synthesis outcomes. Characterization techniques, including N2 physisorption, H2-TPR, XRD, NH3-TPD, and Py-FTIR, were employed to understand the physicochemical properties of these catalysts. Experimental results demonstrated significant improvements in jet fuel selectivity, achieving up to 51.3% selectivity and a productivity of 174.7 g/kgcat/h with the Co/Al-TUD-1 catalyst. Further optimization through adjustment of reaction conditions confirmed the potential for industrial-scale SAF production, offering a cleaner, more sustainable approach to addressing fossil fuel shortages.

CAS / MDL: 102-71-6
研究领域: 化学工程 · 能源科学 · 催化材料
✓ 已验证 产品关联 DOI 高影响因子
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RSC Advances · 2019 ·Vol. 9 ·期 71 ·41591-41602 · IF 3.049

Construction of novel Ag/HKUST-1/g-C3N4 towards enhanced photocatalytic activity for the degradation of pollutants under visible light

Yu Qiao,Qian Han,Dong Li,Hongji Li,Bing Wei,Guangbo Che,Wei Jiang,Weisheng Guan

A novel Ag/metal–organic framework/graphitic carbon nitride (Ag/HKUST-1/g-C3N4, AHC) photocatalyst was prepared via an in situ growth strategy and photo-deposition technique for environmental remediation. The as-obtained samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), N2 adsorption–desorption isotherm measurement, UV-vis diffuse reflection spectroscopy (UV-vis DRS), and photoluminescence (PL) spectroscopy. The results indicated that the hybrids have large surface area, mesoporous structure and enhanced visible-light absorption. The as-prepared hybrid samples exhibited considerable improvement in photocatalytic activity and stability for rhodamine B (RhB) degradation under visible light irradiation (λ > 420 nm). In addition, they also have good adsorption properties. Compared to the pure g-C3N4 and Ag/g-C3N4, the 5% AHC photocatalyst showed superior photocatalytic activity. Moreover, 5% AHC exhibits good photocatalytic activity even after four cycles. Additionally, the active species trapping and electron spin resonance (ESR) experiments indicated that h+ and ·OH were the main active species.

研究领域: 环境催化 · 材料化学 · 光化学 · 纳米材料 · 环境污染治理
✓ 已验证 DOI 高影响因子
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JOURNAL OF POLYMER RESEARCH · 2013 ·Vol. 20 ·期 7 ·1-9 · IF 2.019

Sulfonated poly (aryl ether sulfone) containing 1, 3, 4-oxadiazole as proton exchange membranes for medium-high temperature fuel cells

Xu Jingmei,Ren Chunli,Cheng Hailong,Ma Li,Wang Zhe

Double fluoride 2,5-bis(4-fluorophenyl)-1,3,4-oxadiazole (BFO) monomer was synthesized. Copolymerization of BFO, 2,2-bis(4-hydroxypheny)propane (bisphenol A) and 3′3-disulfonate-4′4-dichloro dipheny sulfone (SDCDPS) at different molar ratio resulted in a new poly (aryl ether sulfone) containing 1, 3, 4-oxadiazole polymers (SPAESO). The structures of monomer BFO and copolymer were confirmed by FT-IR and 1 H NMR. The TEM pictures showed that the ion clusters were formed and distributed evenly in SPAESO copolymer matrix. The sulfonated polyoxadiazole membranes exhibited excellent thermal, dimensional and oxidative stability and lower methanol diffusion coefficient. The proton conductivity of SPAESO-3 was 7.5 × 10 −2 Scm −1 at 120 °C while the methanol permeability coefficient of SPAESO-3 was only 2.23 × 10 −7 cm 2 S −1 at 25 °C. According to the comprehensive performance, the sulfonated polyoxadiazole membranes may be the alternative materials as proton exchange membrane for PEMFC at medium-high temperature operation.

研究领域: 高分子化学 · 燃料电池技术 · 功能材料科学
✓ 已验证 DOI 高影响因子
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Autophagy · 2024 · IF 14.6

Spautin-1 promotes PINK1-PRKN-dependent mitophagy and improves associative learning capability in an alzheimer disease animal model

Juan Yi,He-Ling Wang,Guang Lu,Hailong Zhang,Lina Wang,Zhen-Yu Li,Liming Wang,Yihua Wu,Dajing Xia,Evandro F. Fang,Han-Ming Shen

Spautin-1 is a well-known macroautophagy/autophagy inhibitor via suppressing the deubiquitinases USP10 and USP13 and promoting the degradation of the PIK3C3/VPS34-BECN1 complex, while its effect on selective autophagy remains poorly understood. Mitophagy is a selective form of autophagy for removal of damaged and superfluous mitochondria via the autophagy-lysosome pathway. Here, we report a surprising discovery that, while spautin-1 remains as an effective autophagy inhibitor, it promotes PINK1-PRKN-dependent mitophagy induced by mitochondrial damage agents. Mechanistically, spautin-1 facilitates the stabilization and activation of the full-length PINK1 at the outer mitochondrial membrane (OMM) via binding to components of the TOMM complex (TOMM70 and TOMM20), leading to the disruption of the mitochondrial import of PINK1 and prevention of PARL-mediated PINK1 cleavage. Moreover, spautin-1 induces neuronal mitophagy in Caenorhabditis elegans (C. elegans) in a PINK-1-PDR-1-dependent manner. Functionally, spautin-1 is capable of improving associative learning capability in an Alzheimer disease (AD) C. elegans model. In summary, we report a novel function of spautin-1 in promoting mitophagy via the PINK1-PRKN pathway. As deficiency of mitophagy is closely implicated in the pathogenesis of neurodegenerative disorders, the pro-mitophagy function of spautin-1 might suggest its therapeutic potential in neurodegenerative disorders such as AD.Abbreviations: AD, Alzheimer disease; ATG, autophagy related; BafA1, bafilomycin A1; CALCOCO2/NDP52, calcium binding and coiled-coil domain 2; CCCP, carbonyl cyanide m-chlorophenyl hydrazone; COX4/COX IV, cytochrome c oxidase subunit 4; EBSS, Earle’s balanced salt; ECAR, extracellular acidification rate; GFP, green fluorescent protein; IA, isoamyl alcohol; IMM, inner mitochondrial membrane; MAP1LC3/LC3, microtubule associated protein 1 light chain 3; MMP, mitochondrial membrane potential; mtDNA, mitochondrial DNA; nDNA, nuclear DNA; O/A, oligomycin-antimycin; OCR, oxygen consumption rate; OMM, outer mitochondrial membrane; OPTN, optineurin; PARL, presenilin associated rhomboid like; PINK1, PTEN induced kinase 1; PRKN, parkin RBR E3 ubiquitin protein ligase; p-Ser65-Ub, phosphorylation of Ub at Ser65; TIMM23, translocase of inner mitochondrial membrane 23; TOMM, translocase of outer mitochondrial membrane; USP10, ubiquitin specific peptidase 10; USP13, ubiquitin specific peptidase 13; VAL, valinomycin; YFP, yellow fluorescent protein.

研究领域: 神经科学 · 药理学 · 分子生物学 · 细胞生物学
✓ 已验证 DOI PubMed 高影响因子
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Animals · 2025 ·Vol. 15 ·期 23 ·3491 · IF 2.7

Quercetin Enhances the Antibacterial Activity of Polymyxin E Against MCR-1-Positive Bacteria by Inhibiting the Biological Functions of the Cell Membrane

Yongjie Zhang,Liyang Guo,Shun Wang,Jie Zhang,Xinlei Ren,Rui Li,Jichang Li,Chunli Chen

Simple SummaryPolymyxin E is widely considered the last resort for treating multidrug-resistant Gram-negative bacteria. However, due to the emergence of the plasmid-mediated MCR-1 resistance gene, an increasing number of strains have developed resistance to polymyxin E. Additionally, the prevalence ofEscherichia coliin chickens has imposed a heavy burden on the global food and poultry farming industries. This study aimed to investigate the in vitro and in vivo synergistic effects and mechanisms of quercetin (QUE) combined with polymyxin E against MCR-1-positiveE. coliJD37 from chickens. The in vitro and in vivo synergistic effects of QUE and polymyxin E were confirmed through in vitro drug sensitivity tests, growth curves, time-kill curves, agar diffusion tests, and in vivo chick infection experiments. The results showed that QUE restored the sensitivity of polymyxin E toE. coliJD37 and restored the sensitivity of polymyxin E toE. coliJD37 mainly by increasing the permeability of the cell membrane, elevating the fluidity of the cell membrane, increasing the membrane potential, and reducing the expression of the AcrAB-TolC efflux pump and Lipopolysaccharide (LPS) regulatory-related genes. Molecular docking results revealed the key binding sites of QUE to MCR-1.In animal husbandry and livestock farming, with the spread of the plasmid-mediated MCR-1 gene, polymyxin E, as the last line of defense against drug-resistant Gram-negative bacteria, is facing severe challenges. This study investigated the in vitro and in vivo synergistic effects and mechanisms of QUE combined with polymyxin E against MCR-1-positive chickenE. coliJD37. In vitro experiments showed that QUE could restore the sensitivity ofE. coliJD37 to polymyxin E (FIC = 0.34375) and enhance the bactericidal effect of polymyxin E by increasing cell membrane permeability, fluidity, and membrane potential, downregulating the expression of the AcrAB-TolC efflux pump and LPS-related genes. Molecular docking further identified the key residues for QUE binding to the MCR-1 protein. The in vivo chick infection model confirmed that combination therapy increased survival rates, reduced bacterial load in tissues, alleviated pathological damage, and decreased levels of intestinal inflammatory factors. Our results demonstrate the synergistic bactericidal effect of the QUE-polymyxin E combination against MCR-1-positiveE. coliand elucidate its underlying mechanism.

CAS / MDL: 117-39-5 1895296-01-1
✓ 已验证 产品关联 DOI PubMed 高影响因子
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ELECTROCHIMICA ACTA · 2011 · IF 3.65

Graphene oxide nanoribbon and polyhedral oligomeric silsesquioxane assembled composite frameworks for pre-concentrating and electrochemical sensing of 1-hydroxypyrene

Xiaofang Shen,Yan Cui,Yuehong Pang,He Qian

1-Hydroxypyrene (1-OHP) is a ubiquitous metabolite of polycyclic aromatic hydrocarbons (PAHs) and has been widely used as a biomarker for evaluation of human exposure to PAHs. In this paper, an electrochemical sensor consisted of graphene oxide nanoribbon (GON)/octa(3-aminopropyl)octasilae quioxane octahydrochloride (OA-POSS) framework films (GON/OA-POSS) modified electrode for pre-concentrating and sensing of 1-OHP was described. The GON/OA-POSS composite films were prepared by hierarchically layer-by-layer assembly via electrostatic interactions. GON, which has higher electrical conductivity than that of graphene oxide, offers residual π-conjugated systems for adsorption of 1-OHP via π–π stacking interaction. Meanwhile, OA-POSS nanocages make the GON layers frameworked to enhance contacting between GON and 1-OHP. When 1-OHP was pre-concentrated on GON/OA-POSS frameworks modified electrode, the response signal and adsorption stability was enhanced significantly. Differential pulse voltammetry was used for direct determination of 1-OHP. The electrochemical sensor calibration curve had a range of 0.1–12.55   μM ( R   =   0.995) with a detection limit of 0.04   μM. The results showed that the GON/OA-POSS framework films modified electrode established a new way for simple and sensitive analysis of 1-OHP.

研究领域: 环境科学 · 分析化学 · 材料科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2020 · IF 4.192

Dehydration-Induced Carotenoid Cleavage Dioxygenase 1 Reveals a Novel Route for β-Ionone Formation during Tea (Camellia sinensis) Withering

Jingming Wang,Bin Wu,Na Zhang,Mingyue Zhao,Tingting Jing,Yi Wu,YunQing Hu,Feng Yu,Xiaochun Wan,Wilfried Schwab,Chuankui Song

β-Ionone is a carotenoid-derived flavor and fragrance compound with a complex fruity and woody scent, known for its violet aroma. Due to the low odor threshold, β-ionone dramatically affects the aroma and quality of tea. Previous studies have shown that β-ionone increases during tea withering; however, its formation and regulation during the withering process are far from being understood. As dehydration is the most important stress during the withering of the tea leaves, we isolated a dehydration-induced gene belonging to the subfamily of carotenoid cleavage dioxygenases called carotenoid cleavage dioxygenase 1a (CsCCD1a) from Camellia sinensis and expressed it in Escherichia coli. The recombinant protein could generate volatile β-ionone and pseudoionone from carotenoids. CsCCD1a was induced by dehydration stress, and its expression was related to the β-ionone accumulation during tea withering. Overall, this study elucidated that CsCCD1a catalyzes the formation of β-ionone in C. sinensis and enhanced the understanding of the β-ionone formation under multiple stresses during the processing of tea.

研究领域: 植物生物化学 · 农学 · 食品科学 · 分子生物学
✓ 已验证 DOI PubMed 高影响因子
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CELLULAR AND MOLECULAR LIFE SCIENCES · 2024 ·Vol. 81 ·期 1 ·1-22 · IF 6.2

Vitamin B12 ameliorates gut epithelial injury via modulating the HIF-1 pathway and gut microbiota

Feng Chenxi,Yan Jinhua,Luo Ting,Zhang Hong,Zhang Hu,Yuan Yu,Chen Yi,Chen Haiyang

Inflammatory bowel diseases (IBDs) are immune chronic diseases characterized by recurrent episodes, resulting in continuous intestinal barrier damage and intestinal microbiota dysbiosis. Safe strategies aimed at stabilizing and reducing IBDs recurrence have been vigorously pursued. Here, we constructed a recurrent intestinal injury Drosophila model and found that vitamin B12 (VB12), an essential co-factor for organism physiological functions, could effectively protect the intestine and reduce dextran sulfate sodium-induced intestinal barrier disruption. VB12 also alleviated microbial dysbiosis in the Drosophila model and inhibited the growth of gram-negative bacteria. We demonstrated that VB12 could mitigate intestinal damage by activating the hypoxia-inducible factor-1 signaling pathway in injured conditions, which was achieved by regulating the intestinal oxidation. In addition, we also validated the protective effect of VB12 in a murine acute colitis model. In summary, we offer new insights and implications for the potential supportive role of VB12 in the management of recurrent IBDs flare-ups.

研究领域: 胃肠病学 · 微生物学 · 分子生物学 · 营养学
✓ 已验证 DOI 高影响因子
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MOLECULAR NUTRITION & FOOD RESEARCH · 2022 ·Vol. 66 ·期 23 ·2200300 · IF 6.575

GPR109a Regulates Phenotypic and Functional Alterations in Macrophages and the Progression of Type 1 Diabetes

Zhaodi Zhang,Jiahong Li,Ming Zhang,Binbin Li,XiaoHua Pan,Xiaoliang Dong,Li-Long Pan,Jia Sun

Scope Dietary fibers can alter gut microbiota and microbial metabolite profiles. SCFAs are produced by bacterial fermentation of fiber, mediating immune homeostasis through G-protein-coupled receptors (GPCRs). GPR109a, a receptor for niacin and butyrate, expressed by immune cells and non-immune cells, is a key factor regulating immune responses. However, the role and underlying mechanisms of GPR109a in type 1 diabetes (T1D) remain unclear. Methods and results Experimental T1D was induced by streptozotocin in GPR109a-deficient ( Gpr109a −/− ) and wild type mice. The study found that Gpr109a −/− mice were more susceptible to T1D with dysregulated immune responses, along with increased M1 macrophage polarization (from 10.55% to 21.48%). Further, an adoptive transfer experiment demonstrated that GPR109a-deficient macrophages promoted the homing of intestine-derived type 1 cytotoxic T cells to pancreas (from 18.91% to 24.24%), thus disturbing the pancreatic immune homeostasis in non-obese diabetic mice. Mechanistically, GPR109a deficiency promoted M1 macrophage polarization associated with the activation of suppressor of cytokine signaling 3-signal transducer and activator of transcription 1 signaling pathway. Conclusion The findings reveal that macrophage GPR109a deficiency accelerates the development of T1D. Activation of GPR109a on macrophage by dietary components may provide a new strategy for preventing or treating T1D.

研究领域: 免疫学 · 内分泌学 · 代谢学 · 胃肠病学
✓ 已验证 DOI PubMed 高影响因子
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