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中国精品科技期刊2020
李静,王翔宇,张诗琦,等. 牦牛酸乳源高产胞外多糖乳酸菌筛选及其多糖结构表征与体外功能活性分析J. 食品工业科技,2026,47(9):190−202. doi: 10.13386/j.issn1002-0306.2025050164.
引用本文: 李静,王翔宇,张诗琦,等. 牦牛酸乳源高产胞外多糖乳酸菌筛选及其多糖结构表征与体外功能活性分析J. 食品工业科技,2026,47(9):190−202. doi: 10.13386/j.issn1002-0306.2025050164.
LI Jing, WANG Xiangyu, ZHANG Shiqi, et al. Screening of High-yield Exopolysaccharide-producing Lactic Acid Bacteria from Yak Fermented Milk and Structural Characterization and in Vitro Bioactivity Analysis of PolysaccharidesJ. Science and Technology of Food Industry, 2026, 47(9): 190−202. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025050164.
Citation: LI Jing, WANG Xiangyu, ZHANG Shiqi, et al. Screening of High-yield Exopolysaccharide-producing Lactic Acid Bacteria from Yak Fermented Milk and Structural Characterization and in Vitro Bioactivity Analysis of PolysaccharidesJ. Science and Technology of Food Industry, 2026, 47(9): 190−202. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025050164.

牦牛酸乳源高产胞外多糖乳酸菌筛选及其多糖结构表征与体外功能活性分析

Screening of High-yield Exopolysaccharide-producing Lactic Acid Bacteria from Yak Fermented Milk and Structural Characterization and in Vitro Bioactivity Analysis of Polysaccharides

  • 摘要: 本研究旨在从川西传统牦牛酸乳中筛选高产胞外多糖(Exopolysaccharides,EPS)的乳酸菌,并对其所产EPS进行结构表征与功能特性分析。从185株分离自酸牦牛乳的乳酸菌中筛选出一株高产EPS的菌株——发酵粘液乳杆菌197(Limosilactobacillus fermentum 197)。通过单因素实验优化其发酵培养基组成,并采用DEAE-52和CL-6B柱层析对EPS进行分离纯化,得到主要组分EPS1,利用傅里叶变换红外光谱、凝胶渗透色谱及核磁共振等技术对EPS1的结构进行解析,并评估其体外抗氧化和血糖调节活性。结果表明,该菌在优化后的培养基(麦芽糖与大豆蛋白胨均为40 g/L)中EPS产量达到1699.83±34.31 mg/L,较原始产量提高5倍。纯化后组分EPS1得率为15.07%,分子量为2.11×105 Da,主要由鼠李糖、阿拉伯糖、半乳糖、葡萄糖和甘露糖组成,含有αβ型糖苷键,具备三股螺旋结构,微观呈片状多孔形态。体外活性研究表明,EPS1在10 mg/mL浓度下对ABTS+自由基、DPPH自由基和羟基自由基的清除率分别为57.07%、46.54%和49.68%,对α-淀粉酶的抑制率为51.46%。本研究揭示了EPS1的结构与其抗氧化和降血糖活性之间的关联,为开发基于乳酸菌EPS的功能性乳制品提供了理论依据,也为高原乳酸菌资源的综合利用提供了新方向。

     

    Abstract: This study aimed to screen lactic acid bacteria (LAB) with high exopolysaccharide (EPS)-producing capacity from traditional yak yogurt in Western Sichuan, and to characterize the structure and functional properties of the EPS. Among 185 LAB strains isolated, Limosilactobacillus fermentum 197 was identified as a high EPS producer. The fermentation medium was optimized through single-factor experiments, and the EPS was purified using DEAE-52 and CL-6B column chromatography. The purified fraction EPS1 was structurally characterized by Fourier-transform infrared spectroscopy, gel permeation chromatography, and nuclear magnetic resonance, and its bioactivities were evaluated in vitro. The results showed that the optimal carbon and nitrogen sources for EPS production were maltose and soybean peptone, both at 40 g/L. After optimization, the EPS yield reached 1699.83±34.31 mg/L, representing a 5-fold increase compared to the original yield. The purified EPS1, with a yield of 15.07%, had a molecular weight of 2.11×105 Da and was composed of rhamnose, arabinose, galactose, glucose, and mannose. It contained both α- and β-glycosidic bonds, exhibited a triple-helix structure, and displayed a flaky porous morphology under microscopy. In vitro assays demonstrated that EPS1 at 10 mg/mL exhibited scavenging rates against ABTS+, DPPH, and hydroxyl radicals of 57.07%, 46.54%, and 49.68%, respectively, and an α-amylase inhibition rate of 51.46%. This study reveals the relationship between the structure of EPS1 and its antioxidant and hypoglycemic activities, providing a theoretical basis for developing functional dairy products using LAB-derived EPS and offering new insights into the utilization of lactic acid bacteria resources from plateau pastoral areas.

     

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