Conformation and anticancer activity of a novel mannogalactan from the fruiting bodies of Sanghuangporus sanghuang on HepG2 cells

被引:21
|
作者
Cheng, Junwen [1 ]
Song, Jiling [2 ]
Wang, Yanbin [1 ]
Wei, Hailong [1 ]
He, Liang [1 ]
Liu, Yu [3 ]
Ding, Hongmei [4 ]
Huang, Qingrong [5 ]
Hu, Chuanjiu [1 ]
Huang, Xubo [1 ]
Jiang, Yihan [1 ,6 ]
Wu, Youliang [7 ]
机构
[1] Zhejiang Acad Forestry, Dept Forest Foods, Key Lab Biol & Chem Utilizat Zhejiang Forest Reso, Hangzhou 310023, Peoples R China
[2] Hangzhou Acad Agr Sci, Hangzhou 310024, Peoples R China
[3] Zhejiang Univ, Coll Life Sci, Inst Biochem, Hangzhou 310058, Peoples R China
[4] Zhejiang Chinese Med Univ, Hangzhou 310053, Peoples R China
[5] Rutgers State Univ, Dept Food Sci, 65 Dudley Rd, New Brunswick, NJ 08901 USA
[6] Zhejiang A&F Univ, Hangzhou 311300, Peoples R China
[7] Characterist Plantat Technol Extens Ctr Jiangshan, Jiangshan 324199, Zhejiang, Peoples R China
关键词
Sanghuangporus sanghuang; Polysaccharide; Structural characterization; Chain conformation; Surface topographies; Anticancer activity; STRUCTURAL-CHARACTERIZATION; ANTITUMOR-ACTIVITY; ACIDIC POLYSACCHARIDE; CHAIN CONFORMATION; IN-VITRO; ANTIOXIDANT; ELUCIDATION; HETEROPOLYSACCHARIDE; APOPTOSIS;
D O I
10.1016/j.foodres.2022.111336
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A novel water-soluble mannogalactan (SSPS1) with an average molecular weight of 2.04 x 10(4) Da was obtained from the fruiting bodies of the Sanghuangporus sanghuang. It revealed that SSPS1 was composed of D-galactose, Dmannose, L-fucose, 3-O-methylgalactose and D-glucose in a ratio of 6.2:3.9:3.1:2.1:1.0. The structural elucidation of SSPS1 consisted of 1, 6-linked a-D-Galp, 1, 6-linked a-D-Manp and 1, 6-linked 3-O-methyl- a-D-Galp backbone with branching at O-2 of 1, 6-alpha-D-mannosyl residues by a-L-Fucp and a-D-Glcp units. The conformational parameters suggested that a flexible chain conformation of SSPS1 in solution based on light scattering and atomic force microscopy imaging. Intriguingly, it presented potent anticancer activity on HepG2 cell with Rq and Ra values increased dramatically up to 73.93 nm and 53.92 nm compared with the control. The analysis of flow cytometry indicated SSPS1 could induce the apoptosis of HepG2 cells and arrest them via S phase. Western blot assay further uncovered that apoptosis process was triggered by SSPS1 via a mitochondria-mediated signaling pathway, which was evidenced by an increased ratio of Bax/Bcl-2, the release of cytochrome c and the strong activation of caspase-3 and 9. Taken together, these results suggested that SSPS1 might be applied in functional food as an anticancer agent.
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页数:11
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