{"title":"Selective Protein and Lipid Cargo Sorting into Extracellular Vesicles of Lacticaseibacillus paracasei subsp. paracasei.","authors":"Huixue Hu, Ming Yang, Jiamu Kang","doi":"10.1007/s12602-026-11239-9","DOIUrl":null,"url":null,"abstract":"<p><p>Extracellular vesicles (EVs) are nanoscale lipid bilayer particles that transport bioactive cargo. EVs from lactic acid bacteria show health benefits and drug-delivery potential, yet cargo encapsulation remains understudied. Here, EVs were isolated, purified, and characterized from the bacteriocin-producing strain Lacticaseibacillus paracasei subsp. paracasei YCL29, which was isolated from fermented Yucha. Proteomic and lipidomic analyses were subsequently conducted to compare the EVs with their parental L. paracasei YCL29 cells. Nanoflow cytometry indicated EVs with mean diameter 86.0 ± 18.8 nm at 4.83 × 10<sup>9</sup> particles/mL. Proteomic analysis identified 2,120 high-confidence proteins and revealed selective cargo sorting, with 313 proteins enriched in EVs and 446 downregulated relative to the parent cells. EV-enriched proteins were associated with stress tolerance, nutrient transport/metabolism, nucleic acid metabolism, catalysis, and antibiotic biosynthesis, including cold-shock and antioxidant proteins were detected under non-stress conditions. Lipidomic analysis showed enrichment of phosphatidylethanolamine and triglycerides, defining a distinct EV lipid signature. These findings provide insights into potential cargo-sorting mechanisms and functions of L. paracasei EVs.</p>","PeriodicalId":20506,"journal":{"name":"Probiotics and Antimicrobial Proteins","volume":" ","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2026-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Probiotics and Antimicrobial Proteins","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s12602-026-11239-9","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Extracellular vesicles (EVs) are nanoscale lipid bilayer particles that transport bioactive cargo. EVs from lactic acid bacteria show health benefits and drug-delivery potential, yet cargo encapsulation remains understudied. Here, EVs were isolated, purified, and characterized from the bacteriocin-producing strain Lacticaseibacillus paracasei subsp. paracasei YCL29, which was isolated from fermented Yucha. Proteomic and lipidomic analyses were subsequently conducted to compare the EVs with their parental L. paracasei YCL29 cells. Nanoflow cytometry indicated EVs with mean diameter 86.0 ± 18.8 nm at 4.83 × 109 particles/mL. Proteomic analysis identified 2,120 high-confidence proteins and revealed selective cargo sorting, with 313 proteins enriched in EVs and 446 downregulated relative to the parent cells. EV-enriched proteins were associated with stress tolerance, nutrient transport/metabolism, nucleic acid metabolism, catalysis, and antibiotic biosynthesis, including cold-shock and antioxidant proteins were detected under non-stress conditions. Lipidomic analysis showed enrichment of phosphatidylethanolamine and triglycerides, defining a distinct EV lipid signature. These findings provide insights into potential cargo-sorting mechanisms and functions of L. paracasei EVs.
期刊介绍:
Probiotics and Antimicrobial Proteins publishes reviews, original articles, letters and short notes and technical/methodological communications aimed at advancing fundamental knowledge and exploration of the applications of probiotics, natural antimicrobial proteins and their derivatives in biomedical, agricultural, veterinary, food, and cosmetic products. The Journal welcomes fundamental research articles and reports on applications of these microorganisms and substances, and encourages structural studies and studies that correlate the structure and functional properties of antimicrobial proteins.