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中国精品科技期刊2020
李鑫,黄诗凡,仇晨晨,等. 低温酶法超声提取灰树花多糖抗氧化、酪氨酸酶抑制和降脂活性研究J. 食品工业科技,2026,47(20):1−11. doi: 10.13386/j.issn1002-0306.2025060293.
引用本文: 李鑫,黄诗凡,仇晨晨,等. 低温酶法超声提取灰树花多糖抗氧化、酪氨酸酶抑制和降脂活性研究J. 食品工业科技,2026,47(20):1−11. doi: 10.13386/j.issn1002-0306.2025060293.
LI Xin, HUANG Shifan, QIU Chenchen, et al. Study on the Antioxidant, Tyrosinase Inhibitory and Lipid-lowering Activities of Grifola frondosa Polysaccharides Extracted by Low-temperature Enzymatic UltrasoundJ. Science and Technology of Food Industry, 2026, 47(20): 1−11. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025060293.
Citation: LI Xin, HUANG Shifan, QIU Chenchen, et al. Study on the Antioxidant, Tyrosinase Inhibitory and Lipid-lowering Activities of Grifola frondosa Polysaccharides Extracted by Low-temperature Enzymatic UltrasoundJ. Science and Technology of Food Industry, 2026, 47(20): 1−11. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025060293.

低温酶法超声提取灰树花多糖抗氧化、酪氨酸酶抑制和降脂活性研究

Study on the Antioxidant, Tyrosinase Inhibitory and Lipid-lowering Activities of Grifola frondosa Polysaccharides Extracted by Low-temperature Enzymatic Ultrasound

  • 摘要: 多糖是灰树花(GF)重要活性物质之一,本文旨在优化灰树花多糖(GFP)的提取工艺,并对其抗氧化、酪氨酸酶抑制和降脂活性进行评估。通过乙醇对GF子实体进行前处理,采用超声波辅助复合酶法在低温下提取灰树花多糖,经优化得最佳工艺条件为料液比1:30(g/mL),酶解pH=7,酶解时间100 min,酶解温度60 ℃,超声功率400 W,在此条件下GFP得率为26.37%±0.49%。实验结果表明,GFP的抗氧化活性呈浓度依赖性,在3.0 mg/mL时,其对DPPH、羟基自由基、O2及ABTS自由基的清除率分别达78%、55%、80%和60%,且其总还原力在3.0 mg/mL时吸光度值达到0.54,表现出较强的电子供给能力。GFP可抑制油酸诱导的HepG2细胞脂质积累,100 μg/mL的GFP孵育细胞24 h,细胞内脂质甘油三酯(TG)和总胆固醇(TC)分别降低35.6%和31.7%。Western blot检测结果表明,高浓度灰树花多糖提高了PPARγ,p-FOXO1的蛋白表达水平,降低了G6Pase的蛋白表达水平。该研究优化了GFP的高效绿色提取工艺,并发现了GFP的酪氨酸酶抑制作用,在质量浓度为3.0 mg/mL时,GFP的酪氨酸酶抑制率达20%~30%。结合其抗氧化及降脂活性,为灰树花在功能性食品、保健品及化妆品原料拓展等领域的开发应用提供了重要的理论与实验依据。

     

    Abstract: Polysaccharides are one of the key bioactive components of Grifola frondosa (GF). This study aimed to optimize the extraction process of Grifola frondosa polysaccharide (GFP) and evaluate its antioxidant, tyrosinase inhibition, and lipid-lowering activities. After pretreatment of GF fruiting bodies with ethanol, the GFP was isolated by low-temperature ultrasound-assisted compound enzymatic extraction. The optimal extraction conditions were determined as follows: solid-liquid ratio of 1:30 (g/mL), enzymatic pH of 7.0, enzymatic duration of 100 minutes, enzymatic temperature of 60℃, and ultrasonic power of 400 W. Under these conditions, the yield of GFP was 26.37%± 0.49%. The results showed that GFP's antioxidant activity was concentration-dependent. When the concentration was 3.0 mg/mL, the scavenging rates against DPPH free radicals, hydroxyl free radicals, superoxide anion (O2-), and ABTS free radicals were 78%, 55%, 80%, and 60%, respectively. Moreover, its total reducing power showed an absorbance value of 0.54 at 3.0 mg/mL, indicating a significant electron-donating ability. Furthermore, GFP inhibited oleic acid-induced lipid accumulation in HepG2 cells. Treatment with 100 μg/mL of GFP for 24 hours decreased intracellular triglyceride (TG) and total cholesterol (TC) levels by 35.6% and 31.7%, respectively. Western blot analysis revealed that a high concentration of GFP upregulated PPARγ and p-FOXO1 protein levels, while downregulating G6Pase expression. This study optimized an efficient green extraction process for GFP and discovered its tyrosinase inhibition activity. At a mass concentration of 3.0 mg/mL, GFP exhibited a tyrosinase inhibition rate of 20%~30%. Combined with its antioxidant and lipid-lowering properties, these findings provide crucial theoretical and experimental support for the development of Grifola frondosa applications in functional foods, health supplements, and cosmetic ingredients.

     

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