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Food Bioscience · 2026 · IF 6.2

Screening and functional characterization of purine-degrading Limosilactobacillus fermentum R-9 and its active enhancement effect in the fermentation of Smilax glabra Roxb

Xi Hu,Ruxuan Tan,Xueling Qin,Qingyun He,Zhihua Huang,Lizhong Nong,Junwei Qin,Zhenqiang Wu

Hyperuricemia is associated with dietary purine intake, dysregulated purine metabolism, and impaired uric acid excretion. This study aimed to isolate multifunctional LAB from fermented foods and apply the selected strain to enhance the functional potential of Smilax glabra Roxb. fermentation. Among 79 isolates, 46 were identified as LAB. Limosilactobacillus fermentum R-9 showed efficient degradation of inosine, guanosine, and adenosine, while exhibiting favorable gastrointestinal tolerance and safety-related probiotic properties. Its survival rates after simulated gastric and intestinal digestion were 82.28% and 67.18%, respectively. Genomics revealed genes related to nucleoside hydrolysis, purine/pyrimidine transport, nucleotide salvage, starch utilization, α-glucan metabolism, and β-glucosidase-related glycoside transformation, supporting the dual potential of R-9 for purine metabolism and adaptation to starch-rich S. glabra . L. fermentum R-9 was further used to ferment Smilax glabra Roxb., a starch-rich medicinal and edible plant material containing flavonoid glycosides. After 4 days of fermentation, total phenolics increased from 0.384 to 0.572 mg GAE/mL, and total flavonoids increased from 2.11 to 3.02 mg RE/mL. Xanthine oxidase (XOD) inhibitory activity increased from 16.58% to 70.81%, accompanied by enhanced DPPH and ABTS radical-scavenging activities. Astilbin reached 59.75 μg/mL, increasing by 33.79%. Mechanistically, L. fermentum R-9 fermentation promoted acidification, amylase and β-glucosidase activities, starch matrix disruption, and flavonoid release. These findings highlight L. fermentum R-9 as a promising starter for developing fermented Smilax glabra Roxb. products with enhanced antioxidant and xanthine oxidase inhibitory potential.

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BIOCHEMICAL SYSTEMATICS AND ECOLOGY · 2026 · IF 2.2

Chemotype differentiation and environmental drivers of bioactive metabolites in Cordyceps chanhua from diverse geographical origins

Qiucheng Luo,Gangxiang Fei,Xiaoguang Tian,Shuang Han,Jingqiang Guan,Bo Song,Longzhan Gan,Yeming Zhou,Zhijie Wang,Hongbo Lan,Xiao Zou

Two chemotypes, CTA and CTB, were identified in Cordyceps chanhua for the first time. • Intracellular nucleosides were key markers of chemotype differentiation. • CTA showed significantly higher intracellular uridine, guanosine, adenosine, and HEA than CTB. • Altitude and precipitation were the major environmental factors associated with chemotype differentiation. • Intracellular nucleosides showed significant negative correlations with altitude and precipitation and strong positive correlations with each other. Cordyceps chanhua is a valuable medicinal and edible fungus with great potential for functional food development because of its bioactive metabolites with significant pharmacological activities. However, samples from different geographical origins show significant variations in metabolite composition and content. Existing studies are mostly limited to local regions and lack systematic evaluation based on multi-regional samples, particularly regarding chemotype classification and its environmental driving mechanisms. Therefore, this study systematically analyzed the differences in bioactive metabolites, chemotype differentiation patterns, and their environmental driving factors using multi-regional samples. A total of 123  C. chanhua samples were collected from 16 regions across 8 provinces in China. Key bioactive metabolites, including uridine, guanosine, adenosine, N6-(2-hydroxyethyl)-adenosine (HEA), cordycepic acid, extracellular polysaccharides, and ergosterol, were determined in liquid fermentation broth. The results showed significant geographical differences in metabolite accumulation. Hierarchical cluster analysis (HCA) and principal component analysis (PCA) classified the samples into two chemotypes, Chemotype A (CTA) and Chemotype B (CTB). CTA exhibited significantly higher intracellular nucleoside contents than CTB ( p  < 0.01), and intracellular nucleosides were identified as the core variables driving chemotype differentiation. Environmental analysis showed that CTA was mainly distributed in low-altitude and low-precipitation regions, while intracellular nucleosides were significantly negatively correlated with altitude and precipitation. Correlation network analysis further revealed synergistic accumulation patterns among multiple metabolites. This study revealed the geographical variation characteristics of bioactive metabolites in C. chanhua , identified its chemotypes for the first time, and clarified that intracellular nucleosides are key chemical markers for chemotype classification. Download: Download high-res image (340KB) Download: Download full-size image

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FOOD CHEMISTRY · 2026 · IF 10.4

Soft matter-engineered pH-responsive hydrogels for encapsulation, protection, and controlled intestinal release of probiotics (Lacticaseibacillus paracasei YWC-01)

Xiaoyu Cao,Sisheng Li,Qianqian Xu,Zilun Lei,Bo Jiao,David Julian McClements,Hai Yan

pH-responsive hydrogel microcapsules were fabricated from pea protein isolate (PPI) and low-methoxyl pectin (LMP) for the targeted intestinal delivery of Lacticaseibacillus paracasei YWC-01, a probiotic capable of biodegrading uric acid precursors in vitro . Microgels with interpenetrating networks were fabricated via emulsion-templating: probiotics, PPI, LMP, CaCl₂, and glucono-δ-lactone were emulsified in oil and crosslinked by Ca 2+ . Optimized formulation (5% w / v PPI) achieved 94.80% encapsulation efficiency. Microgel size (43–63 μm) was controlled by adjusting Span 80 surfactant concentration. FTIR confirmed probiotic encapsulation via noncovalent interactions, while TEM revealed bacterial clustering within hydrogel voids. In vitro digestion demonstrated exceptional protection: encapsulated probiotics maintained >9 log 10 CFU/g viability (<0.4 log reduction), versus 3.2 log reduction in free cells. Metabolomics indicated encapsulation preserved bioactivity and significantly upregulated functional metabolites potentially enhancing gut microbiota modulation and anti-inflammatory effects. This work establishes an effective oral delivery platform that significantly enhances probiotic gastrointestinal survival and enables targeted release.

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ANALYTICA CHIMICA ACTA · 2026 · IF 6.1

Pyrene trisulfonic acid-functionalized silica-based multi-mode stationary phase for separation of hydrophilic, hydrophobic compounds and rare earth ions

Yali Yang,Hui Ding,Kaijun Quan,Hongwei Zhao,Mingxia Sun,Zhimin Yang,Xiuhui Liu,Hongdeng Qiu,Jia Chen

Background To address the limitations of traditional single-mode stationary phases in separating complex samples, mixed-mode or multi-mode chromatographic stationary phases, which can provide two or more interaction mechanisms, have attracted extensive research interest. Among them, sulfonated pyrene derivatives present a promising candidate ligand, as they synergistically retain the hydrophobicity and π-π interaction capability of the pyrene moiety along with the hydrophilicity and strong cation-exchange capacity provided by the sulfonic acid groups. This synergistic multi-mechanism design significantly enhances separation selectivity for diverse and complex components. Results A pyrene trisulfonic acid-functionalized silica stationary phase (Sil-PyTSa) was successfully prepared and evaluated. In hydrophilic interaction liquid chromatography (HILIC) mode, Sil-PyTSa could efficiently separate nucleobases and nucleosides, ginsenosides, and alkaloids. For nucleobases and nucleosides, it utilized hydrophilic, electrostatic, and π-π interactions, showing superior retention and selectivity over a control HILIC column. In reversed-phase liquid chromatography (RPLC) mode, favorable separation of PAHs was achieved via hydrophobic and π-π interactions, enabling faster analysis and lower solvent consumption than a C18 column. In ion-exchange chromatography (IEC) mode, baseline separation of 14 rare earth elements (REEs) and removal of Fe/U impurities were accomplished. The column efficiency reached 95,920 N/m for naphthalene. Additionally, Sil-PyTSa achieved effective separation for REEs and iron (Fe) in a simulated NdFeB leaching solution and detected nucleobases and nucleosides in Angelica, indicting promising potential for analyzing complex matrices. Significance and novelty This work developed a novel multi-mode chromatographic stationary phase with multiple interactions mechanisms to enable high-performance separations in HILIC, RPLC, and IEC modes. It demonstrates good separation efficiency and selectivity, low solvent consumption, and high stability. This offers a versatile and green solution for the separation of complex samples with diverse analytes.

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Talanta Open · 2026 · IF 5.1

Novel boronate affinity molecularly imprinted nanomaterials for selective dispersive magnetic solid-phase extraction of catecholamines from equine urine

Mei Liu,Xuehong Min,Die Hu,Xiaonan Zhang,Siyi Zhang

In this study, we developed catechol-imprinted magnetic molecularly imprinted polymers (Ca-DFFPBA-MMIPs) via a dual-affinity strategy combining boronate affinity and a two-step template immobilization protocol. The Ca-DFFPBA-MMIPs exhibited high affinity and selectivity for catecholamines (norepinephrine, epinephrine, and dopamine) under neutral conditions. The adsorption capacity reached a plateau at pH 6.5–7.0, and the adsorption time was optimized to 40 minutes. The MMIPs showed excellent selectivity for the target catecholamines over structurally related interferents. The Ca-DFFPBA-MMIPs also demonstrated good reusability, retaining ≥90% of their initial adsorption capacity after seven consecutive cycles. The analytical performance of the Ca-DFFPBA-MMIPs was validated in terms of linear range, coefficient of determination (R²), limit of detection (LOD), limit of quantification (LOQ), and intra- and inter-day precision (RSD). The LODs were 12–31 ng mL⁻¹ and LOQs were 40–103 ng mL⁻¹, with RSDs of 0.87–1.13% (intra-day) and 1.75–1.95% (inter-day). The Ca-DFFPBA-MMIPs were successfully applied to the selective extraction of catecholamines from equine urine (enrichment factors of 18–27), with recoveries ranging from 64.5% to 105.7%. This study provides a new approach for the analysis of catecholamines in complex matrices and highlights the potential of Ca-DFFPBA-MMIPs as a practical nanosorbent for efficient and selective enrichment of catecholamines and related compounds.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2026 · IF 8.7

Multifunctional carboxymethyl chitosan-based supramolecular-polymeric hydrogel with integrated antibacterial and anti-inflammatory activities for accelerated wound healing

Hong Jiang,Xingyu Guo,Luyao Wen,Xinying Zhang,Qingcong Wei

Skin is vulnerable to injuries that can lead to bacterial infection and prolonged inflammation, impeding the healing process. To address this, we developed an antibacterial and anti-inflammatory supramolecular-polymeric composite hydrogel for accelerated wound healing. The hydrogel is formed by integrating paromomycin sulfate-loaded G-quartet (G4) supramolecular nanofibers with a polymeric network of carboxymethyl chitosan grafted with phenylboronic acid (CMCS-PBA). The antibiotic, paromomycin sulfate, was in-situ loaded via dynamic Schiff base linkages with the aldehyde groups on the G4 fibers, enabling a controllable release. While the pure G4 hydrogel is mechanically weak, the introduced CMCS-PBA network significantly enhances the mechanical strength through multi-valent boronate ester bonds and supramolecular co-assembly, making it suitable for wound sites requiring mechanical robustness. The resulting composite hydrogel exhibits excellent tissue adhesion, hemostatic ability, and biocompatibility. It demonstrated potent antibacterial efficacy in vitro and in vivo. In a full-thickness mouse skin wound model, the hydrogel markedly accelerated wound closure and effectively modulated the wound microenvironment by reducing pro-inflammatory cytokines (TNF-α and IL-6) and elevating anti-inflammatory cytokine (IL-10). This work pioneers a synergistic supramolecular-polymeric strategy, yielding a multifunctional platform that surpasses the limitations of traditional single-network hydrogels, offering a versatile therapeutic strategy for managing infected and inflammatory wounds.

CAS / MDL: 118-00-3 83512-85-0
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FOOD CHEMISTRY · 2026 · IF 10.4

The correlation between changes in intrinsic components and formation of hazardous compounds in seven animal-derived foods during roasting at different temperatures

Bo Wang,Feng Zhao,Zheng Zhou,Ji Wang,Lei Qin,Xuhui Huang

Studied hazardous compound changes in the thermal processing of 7 animal foods. • Hazards: acrylamide, 5-hydroxymethylfurfural, 13 heterocyclic aromatic amines. • AA, 5-HMF, and 13 HAAs in all animal foods increased with roasting temperature. • Low moisture and high carbs promoted AA; high protein favored HAAs. • Amino acids and dipeptides had negative correlations with hazardous compounds. The thermal processing of food is often accompanied by changes in composition and the generation of hazardous compounds. However, the unclear mechanisms linking food composition to related hazardous compounds hinder the advancement of inhibition technologies for hazardous compounds formed during thermal processing. In this paper, the mechanisms of 15 kinds of associated hazardous compounds produced by 7 different animal-derived food samples during the roasting process were investigated. When the roasting temperature was 260 °C, mutton exhibited the highest acrylamide content at 0.11 μg/g, chicken had the highest HAAs (heterocyclic aromatic amines) content at 0.17 μg/g, and Antarctic krill showed the highest 5-hydroxymethylfurfural content at 0.72 μg/g. notably, the compounds closely related to the production of associated hazards during thermal processing include amino acids, small dipeptides, and certain carbohydrate compounds. The results of this study have positive significance in improving food safety and optimizing production processes. Download: Download high-res image (136KB) Download: Download full-size image

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JOURNAL OF FOOD COMPOSITION AND ANALYSIS · 2023 · IF 4.3

Development and validation of a HILIC-MS/MS method for simultaneous quantitative of taste-active compounds in foods

Ran Xin,Meng Dong,Yu-Ying Zhang,Xu-Hui Huang,Xiu-Ping Dong,Lei Qin

Taste-active compounds are significant for the taste and nutrition of food, but their simultaneous quantification remains challenging due to the lack of efficient methods. The existing methods are difficult to simultaneously quantify many species and quantities of taste-active compounds by a single assay. In this study, a rapid and reliable method based on hydrophilic interaction chromatography coupled with triple quadrupole-tandem mass spectrometry (HILIC-MS/MS) was established for the simultaneous quantification and validation of 51 taste-active compounds in different food samples. The established method had a wide linear range (0.1–3000 ng/mL) and the limits of quantification were within the range from <0.1 to 100 ng/mL. This method demonstrated good quantification recovery in the range of 60–130 %. With the method proposed, the simultaneous determination of 51 taste-active compounds in 25 food samples was successfully applied. The quantitative and comparative results of taste-active compounds in different food products reveal the chemical characteristics and differences among different types of foods. This method showed good performance and a good application prospect for the simultaneous quantification of taste-active compounds in food samples. The analysis of key taste-active compounds in various food raw materials can enrich the diversification and individual flavor customization needs of food flavorings.

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FOOD AND CHEMICAL TOXICOLOGY · 2023 · IF 4.3

Formation of RNA adducts resulting from metabolic activation of spice ingredient safrole mediated by P450 enzymes and sulfotransferases

Xin Wang,Guangyun Ran,Yufen Liao,Bowen Gong,Chutian Wu,Rong Tan,Ying Liu,Shiyu Zhang,Ying Peng,Weiwei Li,Jiang Zheng

Safrole (SFL) is an IARC class 2B carcinogen. To better understand the mechanism involved in SFL toxicity, we explored the potential interactions between SFL metabolites and RNA. Three guanosine adducts (G1-G3), two adenosine adducts (A1-A2), and two cytosine adducts (C1–C2) were detected by LC-MS/MS in mouse liver S9 incubations, cultured mouse primary hepatocytes, and liver tissues of mice after exposure to SFL. These adducts were chemically synthesized, and one of the guanosine adducts was structurally characterized by 1 H-NMR. Studies in vitro and in vivo showed that SFL was oxidized by cytochrome P450 enzymes to the corresponding 1′-hydroxyl metabolite which was further metabolized by sulfotransferases to form allylic sulfate esters. The formed reactive intermediate(s) subsequently reacted with bases of RNA, leading to RNA adduction, which could play a partial role in the toxicities of SFL through the alteration of RNA biochemical properties and interruption of RNA functions.

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Journal of Materials Chemistry B · 2023 ·Vol. 11 ·期 6 ·1232-1239 · IF 7

A novel triple-network hydrogel based on borate ester groups: from structural modulation to rapid wound hemostasis

Nan Wang,Kangkang Yu,Kun Li,Xiaoqi Yu

Supramolecular hydrogels have received widespread attention due to their soft texture, strong hygroscopicity, and good biocompatibility. These materials have become particularly attractive for sensing, tissue engineering, fluorescence encoding, wound healing, etc. Inspired by the assembly of G-quadruplexes, we choose the boric acid/polyvinyl alcohol/guanosine system to construct a novel triple-network supramolecular hydrogel “tri-BA@PVA/G” via non-covalent cross-linking, and the effect of the concentration of each component on the hydrogel stability was systematically revealed at the same time. Then, the biocompatibility, shape adaption and optical information storage capacity, the rapid hemostatic ability and the ability of the hydrogel to promote wound healing were confirmed both in vitro and in vivo. These results that predict the properties and reveal prospective applications in the field of wound hemostasis have a certain guiding significance for the subsequent preparation of borate-based triple network hydrogels which can be used as wound hemostatic materials.

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Advanced Science · 2023 ·Vol. 10 ·期 9 ·2206851 · IF 15.1

A H2O2-Supplied Supramolecular Material for Post-irradiated Infected Wound Treatment

Peidong Du,Yanzhe Shen,Baoli Zhang,Shan Li,Minzheng Gao,Ting Wang,Xiaokang Ding,Bingran Yu,Zhen-Gang Wang,Fu-Jian Xu

Photodynamic therapy (PDT) is a light triggered therapy by producing reactive oxygen species (ROS), but traditional PDT may suffer from the real-time illumination that reduces the compliance of treatment and cause phototoxicity. A supramolecular photoactive G-quartet based material is reported, which is self-assembled from guanosine (G) and 4-formylphenylboronic acid/1,8-diaminooctane, with incorporation of riboflavin as a photocatalyst to the G4 nanowire, for post-irradiation photodynamic antibacterial therapy. The G4-materials, which exhibit hydrogel-like properties, provide a scaffold for loading riboflavin, and the reductant guanosine for the riboflavin for phototriggered production of the therapeutic H 2 O 2 . The photocatalytic activity shows great tolerance against room temperature storage and heating/cooling treatments. The riboflavin-loaded G4 hydrogels, after photo-irradiation, are capable of killing gram-positive bacteria (e.g., Staphylococcus aureus ), gram-negative bacteria (e.g., Escherichia coli ), and multidrug resistant bacteria (methicillin-resistant Staphylococcus aureus ) with sterilization ratio over 99.999%. The post-irradiated hydrogels also exhibit great antibacterial activity in the infected wound of the rats, revealing the potential of this novel concept in the light therapy.

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Genes · 2023 ·Vol. 14 ·期 6 ·1287 · IF 3.5

A Preliminary Survey of Transfer RNA Modifications and Modifying Enzymes of the Tropical Plant Cocos nucifera L.

Meng Chu,Yichao Qin,Xiuying Lin,Li Ma,Dehai Deng,Daizhu Lv,Pengcheng Fu,Huan Lin

The coconut (Cocos nuciferaL.) is a commercial crop widely distributed among coastal tropical regions. It provides millions of farmers with food, fuel, cosmetics, folk medicine, and building materials. Among these, oil and palm sugar are representative extracts. However, this unique living species ofCocoshas only been preliminarily studied at molecular levels. Benefiting from the genomic sequence data published in 2017 and 2021, we investigated the transfer RNA (tRNA) modifications and modifying enzymes of the coconut in this survey. An extraction method for the tRNA pool from coconut flesh was built. In total, 33 species of modified nucleosides and 66 homologous genes of modifying enzymes were confirmed using a nucleoside analysis using high-performance liquid chromatography combined with high-resolution mass spectrometry (HPLC-HRMS) and homologous protein sequence alignment. The positions of tRNA modifications, including pseudouridines, were preliminarily mapped using a oligonucleotide analysis, and the features of their modifying enzymes were summarized. Interestingly, we found that the gene encoding the modifying enzyme of 2′-O-ribosyladenosine at the 64th position of tRNA (Ar(p)64) was uniquely overexpressed under high-salinity stress. In contrast, most other tRNA-modifying enzymes were downregulated with mining transcriptomic sequencing data. According to previous physiological studies of Ar(p)64, the coconut appears to enhance the quality control of the translation process when subjected to high-salinity stress. We hope this survey can help advance research on tRNA modification and scientific studies of the coconut, as well as thinking of the safety and nutritional value of naturally modified nucleosides.Keywords:Cocos nucifera;epitranscriptomics;LC-MS/MS;nucleoside misidentification;RNA modification

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