Purification, characterization, and antioxidant activity of polysaccharides from Grifola frondosa by hydrogen peroxide/ascorbic acid-assisted extraction

被引:3
|
作者
Ding, Xi-Min [1 ]
Xu, Ying-Ying [1 ]
Liu, Weiming [2 ]
Wang, Xingli [2 ]
Tang, Meng-Ting [1 ]
Zhang, Xu [1 ]
Gu, Qing [1 ]
Zhou, Tao [1 ]
机构
[1] Zhejiang Gongshang Univ, Sch Food Sci & Biotechnol, Key Lab Food Microbial Technol Zhejiang Prov, Hangzhou 310018, Zhejiang, Peoples R China
[2] Zhejiang Biosan Biotech Co Ltd, 116 Dayuan St,Shuige Ind Zone, Lishui 323010, Zhejiang, Peoples R China
关键词
Grifola frondosa polysaccharide; Extraction method; Antioxidant activity; RAW; 264.7; macrophages; STRUCTURAL-CHARACTERIZATION; WATER EXTRACTION; OPTIMIZATION; HETEROPOLYSACCHARIDE; CELL;
D O I
10.1007/s11694-023-02194-y
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
To increase the production of Grifola frondosa polysaccharides (GFPs), a hydrogen peroxide/ascorbic acid (H2O2/Vc)-assisted extraction method was established. The extraction conditions were optimized by response surface methodology. Purification of the crude GFP by DEAE-52 and Sephadex G100 column chromatography yielded three fractions, GFP0, GFP1, and GFP3. Monosaccharide composition analysis revealed that these GFPs mainly consisted of mannose, glucose, galactose and l-fucose, together with a low proportion of xylose, glucuronic acid and ribose. Chemical antioxidant assays indicated that these GFPs possessed considerable reducing power and radical (DPPH<middle dot>, HO<middle dot> and ABTS<middle dot>+) scavenging abil-ity. They were also observed to availably protect RAW264.7 cells from H2O2-induced oxidative stress, reduce intracellular ROS and MDA levels, and increase intracellular SOD and CAT activities. These GFPs were able to up-regulate the mRNA expression of SOD1, CAT, HO-1 and Nrf2, indicating that regulation of antioxidant enzymes and Nrf2 signaling pathway could be their important antioxidant mechanism.
引用
收藏
页码:797 / 811
页数:15
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