Frontiers in Microbiology
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2025
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IF 4.5
Yue Gao,Binbin Huang,Yunyi Qin,Bing Qiao,Mengfei Ren,Liqing Cao,Yan Zhang,Maozhen Han
Background: Obesity and high fasting blood glucose (FBG) resulting from high-fat diets (HFDs) have emerged as significant public health concerns, garnering increasing attention. Recently, gut microbiota has been linked with metabolic diseases such as type 2 diabetes (T2DM), and its mediating role in dietary supplements has been confirmed. Seeking various dietary supplements to lose body weight (BW) and decrease FBG and explaining the underlying mechanism have become the research hotspots in T2DM studies.Methods: In this study, rutin and proanthocyanidins (PA) were selected as dietary supplements (200 mg/kg × day, oral gavage, 6 weeks) in T2DM mice induced with HFD to assess their efficacy in weight loss, FBG reduction, gut microbiota alterations, and the associated underlying mechanisms.Results: Our findings indicate that rutin was more effective than PA in relieving inflammation and fat hypertrophy, although both significantly reduced BW and FBG within 2 weeks after the intervention. Analysis of 16S rRNA amplicons revealed substantial alterations in the gut microbial community composition of mice administered with PA and rutin compared to HFD-fed mice. Importantly, several core microbes, particularly a series of probiotics, such as Akkermansia, Lactococcus, Odoribacter, Faecalibaculum, and Roseburia were identified, which were significantly correlated with the changes in BW and FBG.Conclusion: Overall, our study highlights that rutin and PA can reduce BW, FBG, and inflammation by modulating the gut microbiota composition, providing novel perspectives for managing and treating weight and FBG concerns in obesity and T2DM patients through dietary supplements in clinical treatment.
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CATALYSIS LETTERS
·
2025
·Vol. 155
·期 5
·1-19
·
IF 2.4
Hu Xinyin,Xiao Guoqing,Chen Chunlin,Chen Chunyan,Zeng Xiang,Li Ruili,Yang Zhengwei
Recently, several emerging pollutants have caused increasing damage to aquatic ecosystems. Reducing antibiotic concentrations in water by visible light is one of the most promising strategies for sustainable development. Here, a Bi 2 S 3 /CeO 2 /Ni(OH) 2 Z-scheme heterojunction photocatalyst was prepared by the hydrothermal method, which could effectively utilize free radicals to degrade tetracycline. Ni(OH) 2 was used for co-catalysing in photodegradation experiments to improve electron transfer and enhance photocatalytic performance. The degradation rate of the Z-scheme heterojunction photocatalyst for 20 mg/L TC was 91.35% after reacting 60 min under visible light irradiation. Besides, it also investigated such operational parameters influencing the photocatalytic reaction as catalyst dosage, initial concentration of tetracycline hydrochloride (TC), and solution pH. Studies using free radical scavenging experiments and electron spin resonance (ESR) measurements demonstrated that hydroxyl radicals (·OH) and superoxide radicals (·O 2 − ) both contributed to the photodegradation of TC. Finally, with high-performance liquid chromatography-mass spectrometry (LC-MS), potential degradation pathways of the intermediate products were logically inferred as well as the photocatalytic mechanism. The experimental results surface that the prepared Z-scheme heterojunction photocatalyst Bi 2 S 3 /CeO 2 /Ni(OH) 2 exhibits superior photocatalytic performance, offering a novel approach to addressing TC contamination in environmental settings. Graphical
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Frontiers in Microbiology
·
2025
·
IF 4.5
Qiuqian Zeng,Xiaomei Lyu
Introduction: Cellobiose 2-epimerase (CE) catalyzes the interconversion of glucosyl and mannosyl groups at the reducing end of β-1,4-linked disaccharides. This enzyme is pivotal for converting lactose into prebiotics like epilactose, offering a potential solution for lactose-intolerant-friendly dairy products. However, current CEs are hindered by pH and thermal instability in milk processing, as their neutral-to-alkaline pH optima clash with milk’s mildly acidic conditions (pH 6.5–6.7), and their poor thermolability requires costly post-processing enzyme removal.Methods: We identified a novel CE from the acidophilic Acidobacteriota bacterium (Acba-CE) and characterized its properties. Its enzymatic activity was assessed under varying pH and temperature conditions, including milk-processing environments.Results: Acba-CE exhibits an acidic pH optimum (6.0), retaining 95% activity at milk pH (6.5). Notably, it undergoes rapid thermal inactivation at pasteurization temperatures, enabling complete enzyme deactivation during standard pasteurization without additional steps. In milk systems, Acba-CE achieves 28.5% lactose-to-epilactose conversion at refrigeration temperatures (10°C), demonstrating strong cold adaptability.Discussion: To our knowledge, this is the first reported CE from the Acidobacteriota phylum, combining acidophilic activity with low-temperature adaptability. Acba-CE represents a breakthrough for in situ dairy modification, eliminating key bottlenecks in milk processing and enabling next-generation functional milk production.
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PHYTOMEDICINE
·
2025
·
IF 8.3
Li Fan,Jian Liu,Lin Li,Xueping Yang,Qingwei Zhao,Lijuan Zhao
Background Echinacoside (ECH), a natural phenylethanoid glycoside, has demonstrated protective effects against type 2 diabetes mellitus (T2DM). However, the mechanism underlying the low bioavailability yet advantageous anti-diabetic of ECH remains unresolved. Purpose To elucidate the mechanism of ECH against T2DM through gut microbiota-mediated host metabolism for the first time. Study design and methods A T2DM mouse model was established using a high-fat diet in combination with streptozotocin injection. The therapeutic effects of ECH against T2DM were evaluated by measuring fasting blood glucose (FBG), insulin resistance, glucose intolerance, blood lipids and organ damage in mice. Fecal 16S rRNA and ITS sequencing techniques were employed to characterize the composition of gut microbiota, followed by analysis of bacterial-fungal trans-kingdom network. Metabolomics was conducted to assess the ECH-induced metabolite profile alterations. Additionally, the predicted mechanism of ECH on T2DM was investigated through measuring the hepatic gluconeogenesis markers and inflammation by western blotting, immunohistochemistry, enzymatic assays and antimicrobial mixture (ABX) experiments. Results ECH exhibited significant protective effects against T2DM, as evidenced by reductions in FBG and fasting insulin levels, improvements in glucose and insulin tolerance, attenuations of hyperlipidemia, and alleviation of liver, kidney, and colon damage in T2DM mice. Furthermore, ECH modulated gut microbiota by decreasing the abundances of conditional pathogenic intestinal bacteria ( Klebsiella and Escherichia-Shigella ) and fungi ( Debarymoyces ), while increasing beneficial bacteria ( Lactobacillus ) and fungi ( Wallemia and Penicillium ). Moreover, ECH could restore the disrupted trans-kingdom network between gut fungi and bacteria, thereby suppressing the inflammation-mediated hepatic gluconeogenesis via downregulation of FBP1, PCK1 and G6PC expression. Correspondingly, ABX experiments indicated that once the regulatory function of gut microbiota imbalance was blocked, the anti-T2DM effects of ECH were weakened, accompanied by a failure to improve the levels of inflammation and key gluconeogenic markers in T2DM mice. Conclusion This study presents novel evidence indicating that ECH alleviates T2DM through inhibiting hepatic gluconeogenesis via gut bacterial-fungal trans-kingdom network reconstruction. These findings suggest that ECH may serve as a promising therapeutic strategy for T2DM management, providing new insights for the prevention and treatment of clinical diabetes and its complications.
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INFRARED PHYSICS & TECHNOLOGY
·
2025
·
IF 3.4
Ping Wang,Bin Duan,Yuanyuan Fan,Min Luo,Liming Tang,Changchun Ding,Tong Liu,Wei Jin,Junshan Hu
A novel upconversion phosphor, Ca 3 (VO 4 ) 2 co-doped with Yb 3+ and Er 3+ , was successfully synthesized via a high-temperature solid-state method. Under 980 nm near-infrared excitation, this material exhibits remarkable upconversion luminescence, with intense green emissions at 527 nm and 550 nm, and a weaker red emission at 657 nm. The optimal doping concentrations were determined to be 0.03 for Yb 3+ and 0.005 for Er 3+ , enabling maximum luminescent efficiency. Spectroscopic investigations including upconversion photoluminescence, excitation, and emission spectra confirmed that the upconversion follows a distinct energy transfer mechanism: Yb 3+ ( 2 F 5/2 ) + Er 3+ ( 4 I 11/2 ) → Yb 3+ ( 2 F 7/2 ) + Er 3+ ( 4 F 7/2 ). In addition to its excellent luminescent properties, the Ca 3 (VO 4 ) 2 : 0.03Yb 3+ /0.005Er 3+ phosphor exhibits reliable optical thermal sensitivity over a wide temperature range (298–673 K), with a peak relative sensitivity of 1.11 % K −1 at 298 K. These outstanding optical characteristics make Ca 3 (VO 4 ) 2 : 0.03Yb 3+ /0.005Er 3+ a promising candidate for display and lighting technologies.
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ANALYST
·
2025
·
IF 3.3
Yang Li,Yikan Zhao,Zhihao Yi,Shitong Han
Timely and accurate diagnosis of RNA viruses, represented by the SARS-CoV-2, is the foundation for protecting people from health threats. Currently, direct detection of viral RNA genes remains the most accurate method. Herein, a rapid, ultrasensitive, and no heating equipment required CRISPR/Cas13a based evanescent wave fluorescence biosensing platform for quantitative detection of the SARS-CoV-2 gene is reported. The collateral effect of CRISPR/Cas13a for RNA is combined with a self-driven enzyme-free hybridization chain reaction (HCR) as a signal amplification step. When the initiator RNA strand is cleaved by Cas13a, the downstream signal amplification induced by HCR is blocked, and a multiple crRNA strategy is used to enhance the cleavage efficiency. The newly designed HCR assemblies are captured by the cDNA-modified optical fiber and generate a higher-intensity fluorescence signal induced by the evanescent field. The CRISPR/Cas13a-HCR evanescent wave fluorescence biosensing platform is capable of detection of SARS-CoV-2 with a LOD of 0.47 copies per μL and the detection time is within 35 min. The spike recovery tests in saliva and high specificity have demonstrated the potential of this method for point-of-care diagnosis. This method is also suitable for the detection of other RNA viruses, without the need to alter any design of the HCR component, and only the corresponding crRNA needs to be replaced.
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BIOCHEMICAL PHARMACOLOGY
·
2020
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IF 4.96
Hongwei Yao,Jingkai Gu,Yuqin Shan,Yani Wang,Xue Chen,Dong Sun,Yingjie Guo
Patients with diabetic mellitus tend to have a poor response to clopidogrel (Clop) due to reduced generation of active metabolite (Clop-AM). However, the underlying mechanism is not elucidated. A type 2 diabetic mellitus (T2DM) rat model was established by combining high-fat diet feeding and low-dose streptozotocin (STZ) injection. The reduced Clop-AM exposure was observed in T2DM rats after oral administration of Clop. However, in vitro liver microsomes incubated with Clop exhibited increased Clop-AM levels in T2DM rats due to a significant decrease in carboxylesterase (CES)1 expression and activity and a significant increase in the expression or activity of CYP1A2 and CYP3A . Interestingly, different from oral administration, the significantly increased C max of Clop-AM was observed in T2DM rats after intravenous injection, with no difference in AUC 0-t and t 1/2 values between the two strains. Meanwhile, in situ single -pass intestinal perfusion study showed lower absorption rate constant ( K a) and effective apparent permeability values ( P eff ) of Clop in T2DM rats than in control rats. It is explained by the increased expression or function of P-glycoprotein (P-gp) and pregnane X receptor (PXR) in duodenum and jejunum of T2DM rats. Moreover, the decreased Clop-AM level in T2DM rats was eliminated by the pretreatment of cyclosporin A , a P-gp inhibitor. It suggests that intestinal absorption, not hepatic metabolism is responsible for the reduced Clop-AM exposure in T2DM rats. P-gp might be the key factor causing the reduction of Clop absorption, consequently making less Clop available for Clop-AM formation.
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Bioengineering & Translational Medicine
·
2024
·
IF 6.1
Jihong Ma,Haiyan Yang,Xue Tian,Fanhu Meng,Xiaoqing Zhai,Aimei Li,Chuntao Li,Min Wang,Guohui Wang,Chunbo Lu,Jingkun Bai
Conventional chemotherapeutic agents are limited by their lack of targeting and penetration and their short retention time, and chemotherapy might induce an immune suppressive environment. Peptide self-assembly can result in a specific morphology, and the resulting morphological changes are stimuli responsive to the external environment, which is important for drug permeation and retention of encapsulated chemotherapeutic agents. In this study, a polypeptide (Pep1) containing the peptide sequences PLGLAG and RGD that is responsive to matrix metalloproteinase 2 (MMP-2) was successfully developed. Pep1 underwent a morphological transformation from a spherical structure to aggregates with a high aspect ratio in response to MMP-2 induction. This drug delivery system (DI/Pep1) can transport doxorubicin (DOX) and indomethacin (IND) simultaneously to target tumor cells for subsequent drug release while extending drug retention within tumor cells, which increases immunogenic cell death and facilitates the immunotherapeutic effect of CD4 + T cells. Ultimately, DI/Pep1 attenuated tumor-associated inflammation, enhanced the body's immune response, and inhibited breast cancer growth by combining the actions of DOX and IND. Our research offers an approach to hopefully enhance the effectiveness of cancer treatment.
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ANALYTICA CHIMICA ACTA
·
2025
·
IF 6
Jinhua Xu,Jinyu Zhang,Wenmin Zhang,Shiye Xie,Lan Zhang
Background Chiral pollutants present significant environmental and health concerns, with neurotoxic amino acid analogs like β-N-methylamino-L-alanine (BMAA) demonstrating enantiomer-specific bioaccumulation in aquatic ecosystems. Current analytical approaches for chiral environmental contaminants rely predominantly on chromatographic techniques that require extensive sample preparation (typically 24 h), limiting field deployment and high-throughput screening capabilities. Detection thresholds for these compounds (0.1–10 μg/L) necessitate sensitive methodologies that maintain stereochemical integrity. This study addresses these analytical challenges through the rational design of chiral cobalt hydroxide (CF–Co(OH) 2 ) nanomaterials engineered for dual-mode detection and separation functionality. Results A hierarchical porous α-Co(OH) 2 with tunable chirality (R/S/RS configurations) and morphologies (square, rough surface, snowflake, flower-like) via micelle-templated growth strategies. The materials demonstrated dual functionality: (1) Rapid colorimetric amino acid discrimination within 5 min with precision (RSD = 4.9 %, n = 6), validated through urinary l -tryptophan quantification (17.1 ± 0.4 μg/mL); (2) Ultrasensitive BMAA separation via SPE-HPLC-MS/MS with significantly improved detection limits (LOD = 0.02 μg/kg) and processing speed (144 × faster than conventional methods). The colorimetric detection mechanism exploits BMAA's ability to form cobalt-amine complexes that produce concentration-dependent yellow coloration, enabling visual detection at 50 μg/kg in freshwater samples. Field testing successfully detected BMAA in crucian carp (0.39 ± 0.03 μg/kg), confirming food-chain biomagnification with excellent recovery (90.1–102.7 %) across diverse matrices. The system's chiral specificity exhibited distinct affinity patterns (BMAA: R–Co(OH) 2 ; DAB: S–Co(OH) 2 ) with 91.4 % enantiomeric excess in just 10 min through configuration-specific “three-point binding” mechanisms (intramolecular binding energy: 18.7 kcal/mol). Significance This research establishes morphology-programmable chiral materials as a versatile analytical platform for rapid on-site environmental monitoring and high-throughput toxin analysis. The developed methodology directly addresses World Health Organization guidelines for algal toxin detection in drinking water while providing a generalizable approach for chiral pollutant discrimination in complex environmental and biological samples.
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Microbiome
·
2025
·Vol. 13
·期 1
·1-21
·
IF 12.7
Zhu Liuying,Zhang Zhiyi,Luo Ting,Li Hongyan,Deng Zeyuan,Li Jing,Zheng Liufeng,Liao Jinqiang,Wang Minghui,Zhang Bing
Background 2′-Fucosyllactose (2′-FL) is one of the major oligosaccharides found in human breast milk, with several recognized beneficial effects on the host. Extensive research has indicated positive effects of 2′-FL on cognitive development in the brain, yet its molecular mechanisms have remained elusive. This study aimed to assess the impact of 2′-FL on the gut-brain axis microbiota and cognitive function in growing mice, along with its potential mechanisms of action.
Results Following long-term supplementation for 4 weeks, 2′-FL was found to enhance cognitive memory function in growing mice (3 weeks old) as assessed through Y-maze, novel object recognition, and water maze tests. Analysis via 16S rRNA sequencing revealed significant alterations in gut microbiota diversity and composition induced by 2′-FL, notably increasing the relative abundance of Bacteroides and Lactobacillus genera. Additionally, 2′-FL significantly elevated levels of 5-hydroxytryptamine (5-HT) and 5-hydroxytryptophan (5-HTP) in the hippocampal tissue. However, antibiotic intervention abolished the cognitive advantage conferred by 2′-FL, highlighting the critical role of gut microbiota in mediating its effects. Similarly, short-term supplementation with 2′-FL for 7 days indicated rapid changes in gut microbiota composition preceding cognitive improvements, further suggesting a potential causal relationship between gut microbiota characteristics and cognition. Further, in vitro experiments with mouse feces suggested that 2′-FL may influence tryptophan hydroxylase levels in the gut microbiota and inhibit the activity of 5-hydroxytryptophan decarboxylase, potentially leading to increased accumulation of 5-HTP. Additionally, 2′-FL may indirectly impact tryptophan hydroxylase levels in enterochromaffin cells by promoting short-chain fatty acid production, which could support 5-HTP synthesis. Elevated 5-HTP produced by the gut system enters the bloodstream, crosses the blood–brain barrier, and may potentially enhance brain 5-HT levels.
Conclusion This study offers preliminary evidence that the cognitive-promoting effects of 2′-FL in mice may be closely associated with gut microbiota and 5-HT. The findings suggest that 2′-FL contribute to cognitive development in growing mice, potentially by modulating gut microbiota and enhancing 5-HT levels in the brain.
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ChemistrySelect
·
2025
·Vol. 10
·期 15
·e202406023
·
IF 2
Leyao Chen,Nuoya Wang,Xiaoyu Chang,Ruiyong Wang
Graphical This work investigated the inhibition of 4-thiazolidinone derivatives on SARS-CoV-2 Mpro using enzyme assays, spectroscopy, and molecular docking. Compound 3a showed the best inhibition (IC 50 = 2.36 ± 0.36 µM, K i = 1.72 µM), and the trifluoromethyl group in 3a played an important role. Hydrogen bonding and van der Waals forces were the main forces for the binding. This work provided clues for Mpro inhibitor development. Since the outbreak of COVID-19, one of the strategies used to search for potential drugs has been to screen inhibitors of SARS-CoV-2 Mpro. This work investigated the inhibitory effects of 4-thiazolidinone derivatives on main protease (Mpro) using various methods, including enzyme activity assays, enzyme kinetics, spectroscopy experiments, molecular docking simulations, microscale thermophoresis, and cytotoxicity tests. Compound 3a demonstrated the best inhibition effect among the compounds tested, with IC 50 = 2.36 ± 0.36 µM and K i = 1.72 µM. The trifluoromethyl group in 3a might enhance its inhibition ability. Interactions between the 4-thiazolidinone derivatives and Mpro resulted in fluorescence quenching primarily through static quenching. Thermodynamic analysis indicated that the interaction forces are mainly hydrogen bonds and van der Waals forces. Spectral results revealed that the 4-thiazolidinone derivatives affected the microenvironment of aromatic amino acid residues in Mpro and altered its secondary structure. Differential scanning fluorimetry was used to confirm the interaction between the 4-thiazolidinone derivatives and Mpro. Results of microscale thermophoresis indicated that the K d between 3a and Mpro was 1.56 ± 0.24 µM. Molecular docking simulations provided a more intuitive visualization of the interaction forces. This study provides clues for screening novel Mpro inhibitors.
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CHEMISTRY-A EUROPEAN JOURNAL
·
2025
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IF 3.7
Zhicheng Tang,Tianwei Wang,Hua Lin,Shoulong Hao,Shufen Zhang,Rongwen Lu
Amination of 1-amino-4-bromoanthraquinone-2-sulfonic acid (BAA), crucial for anthraquinone-type dyes production, relies on Cu+ catalysis. However, Cu+ disproportionation causes catalyst deactivation, requiring large amounts of Cu catalysts (e.g., CuSO4 or CuCl) and reductants (e.g., FeSO4), introducing heavy metals and increasing water consumption to remove byproducts and metals, raising both environmental and economic costs. To address these challenges, we introduce a groundbreaking strategy for the in-situ generation of Cu+ using symmetrical Cu electrodes under alternating current (AC) electrolysis. This method achieves 100% conversion of BAA in the amination with 3,5-diamino-2,4,6-trimethylbenzene sulfonic acid (M Acid) with 95% yield, while also providing a solution to the issue of Cu+ disproportionation without the need for any additional copper catalysts or reductants, demonstrating a broad substrate scope and significantly reducing water usage in post-treatment. Characterization techniques, including X-ray photoelectron spectroscopy, X-ray diffraction, and electrochemical impedance spectroscopy, reveal that the passive Cu2O film formed on the symmetrical Cu electrodes under AC electrolysis continuously generates Cu+, which is crucial for the reaction. This approach is scalable, environmentally friendly, and holds great potential for industrial applications, offering substantial economic benefits while reducing environmental impact.
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