食品科学 ›› 2025, Vol. 46 ›› Issue (22): 236-245.doi: 10.7506/spkx1002-6630-20250603-015

• 生物工程 • 上一篇    下一篇

植物乳植杆菌发酵对人参体外模拟消化中活性物质含量及功能活性的影响

郑志豪,李晓春,林登蕃,周映君,彭源德,宋帅,蔡金文,王海轩,谢纯良   

  1. (1.中国农业科学院麻类研究所,湖南?长沙 410205;2.江苏菌钥生命科技发展有限公司,江苏?盐城 224100)
  • 发布日期:2025-11-21
  • 基金资助:
    国家麻类产业技术体系项目(CARS-16); 中国农业科学院麻类研究所科技创新工程重大任务专项(CAAS-ASTIP-2023-IBFC)

Effect of Lactiplantibacillus plantarum Fermentation on the Contents and Functional Activities of Active Substances in Ginseng during in Vitro Simulated Digestion

ZHENG Zhihao, LI Xiaochun, LIN Dengfan, ZHOU Yingjun, PENG Yuande, SONG Shuai, CAI Jinwen, WANG Haixuan, XIE Chunliang   

  1. (1. Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, Changsha 410205, China; 2. Jiangsu FTCM Life Science & Technology Development Co., Ltd., Yancheng 224100, China)
  • Published:2025-11-21

摘要: 为探究乳酸菌发酵对人参体外模拟消化中活性物质释放及功能活性的影响,本研究建立体外口腔-胃-肠3 段消化模型,结合高效液相色谱技术及功能活性评价体系,系统分析人参经植物乳植杆菌发酵前后在消化过程中总酚、总黄酮、多糖及单体人参皂苷的动态变化规律,并评估其抗氧化活性与降血糖活性。结果表明:在体外模拟消化过程中,乳酸菌发酵显著促进活性物质的释放。在肠消化阶段,发酵组总酚释放量达(3.65±0.11)mg/g,较未发酵组提升30.3%(P<0.05);发酵组总黄酮释放量在胃消化阶段受酸性环境影响短暂下降,但在肠消化后期恢复至(1.18±0.04)mg/g。此外,发酵显著提高了稀有人参皂苷(F2、Rg3、CK、Rh2)在肠消化阶段的释放量,其中发酵组的F2、Rg3、CK和Rh2释放量分别达到了(12.57±0.07)、(8.32±0.54)、(7.25±0.21)mg/g和(1.81±0.12)mg/g,而未发酵组的F2、Rg3、CK和Rh2释放量仅分别为(10.21±0.19)、(0.62±0.13)、(1.43±0.16)mg/g和(0.38±0.07)mg/g。功能活性分析显示,在肠消化阶段,发酵组的2,2’-联氮双(3-乙基苯并噻唑啉-6-磺酸)阳离子自由基清除率、铁离子还原能力、超氧阴离子自由基清除率及α-葡萄糖苷酶抑制率分别为(89.22±3.04)%、0.57±0.01、(41.36±0.96)%和(83.81±0.71)%,较未发酵组分别提升21.8%、15.2%、141.3%和8.3%。相关性分析表明,总酚、多糖和稀有人参皂苷(F2、Rg3、CK)含量与抗氧化活性、降血糖活性呈正相关,而原型皂苷Rg1、Re含量与抗氧化活性及降血糖活性呈负相关。综上,乳酸菌发酵通过酶解作用提前转化原型人参皂苷,协同消化环境进一步促进活性物质的释放与转化,显著提升消化产物的生物利用度与功能活性,本研究可为人参高附加值功能性食品的开发提供理论依据。

关键词: 乳酸菌发酵;人参;体外模拟消化;稀有人参皂苷;抗氧化活性;α-葡萄糖苷酶抑制活性

Abstract: To investigate the effect of lactic acid bacterial fermentation on the release and functional activities of active substances in ginseng during in vitro simulated digestion, this study established an in vitro oral-gastric-intestinal digestion model. High performance liquid chromatography (HPLC) was used to analyze the dynamic changes in total phenols, total flavonoids, polysaccharides, and monomeric ginsenosides during the digestion of ginseng fermented and not fermented with Lactiplantibacillus plantarum. Additionally, the antioxidant activity and hypoglycemic activity of the resulting digests were evaluated. The results indicated that lactic acid bacterial fermentation significantly promoted the release of active substances during in vitro simulated digestion. In the intestinal digestion stage, the release of total phenols from fermented ginseng reached (3.65 ± 0.11) mg/g, which increased 30.3% compared with non-fermented ginseng (P < 0.05). The release of total flavonoids from fermented group temporarily decreased during the gastric digestion stage, due to the acidic environment, but increased to (1.18 ± 0.04) mg/g in the subsequent intestinal digestion. Furthermore, compared with the non-fermented control, fermentation significantly increased the release of the rare ginsenosides F2, Rg3, CK, and Rh2 from (10.21 ± 0.19), (0.62 ± 0.13), (1.43 ± 0.16), and (0.38 ± 0.07) mg/g to (12.57 ± 0.07), (8.32 ± 0.54), (7.25 ± 0.21), and (1.81 ± 0.12) mg/g during the intestinal digestion stage, respectively. After intestinal digestion, the 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical cation scavenging capacity, ferric ion reducing antioxidant power (FRAP), superoxide anion radical scavenging capacity, and α-glucosidase inhibitory activity of fermented ginseng were (89.22 ± 3.04)%, 0.57 ± 0.01, (41.36 ± 0.96)%, and (83.81 ± 0.71)%, respectively, which were 21.8%, 15.2%, 141.3%, and 8.3% higher than those of the non-fermented control, respectively. Correlation analysis revealed that the contents of total phenols, polysaccharides, and rare ginsenosides (F2, Rg3 and CK) were positively correlated with antioxidant and hypoglycemic activities, while the prototype ginsenosides Rg1 and Re were negatively correlated with both activities. In conclusion, lactic acid bacterial fermentation transforms prototype ginsenosides in ginseng through enzymatic hydrolysis, synergizing with the digestive environment to further promote the release and transformation of active substances, significantly enhancing the bioavailability and functional activity of digestive products. This study provides a theoretical basis for developing high-value-added functional foods based on ginseng.

Key words: lactic acid bacterial fermentation; ginseng; in vitro simulated digestion; rare ginsenosides; antioxidant activity; α-glucosidase inhibitory activity

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