Preparation and inhibition on α-D-glucosidase of low molecular weight polysaccharide from Cordyceps militaris

被引:33
|
作者
Zhu, Zhen-Yuan [1 ]
Guo, Ming-Zhu [1 ]
Liu, Fei [1 ]
Luo, You [1 ]
Chen, Lu [1 ]
Meng, Meng [1 ]
Wang, Xiao-Ting [1 ]
Zhang, Yong-Min [2 ]
机构
[1] Tianjin Univ Sci & Technol, Key Lab Food Nutr & Safety, Minist Educ, Coll Food Sci & Biotechnol,Tianjin Econ & Technol, 29,13th Ave, Tianjin 300457, Peoples R China
[2] Univ Pierre & Marie Curie Paris 6, Inst Parisien Chim Mol, CNR UMR 8232, 4 Pl Jussieu, F-75005 Paris, France
关键词
Cordyceps militaris; Acid hydrolysis; Inhibitory activity; ANTITUMOR-ACTIVITY; STRUCTURAL-CHARACTERIZATION; ANTIOXIDANT ACTIVITIES; PURIFICATION; PROPERTY; SINENSIS; MYCELIUM; BODIES;
D O I
10.1016/j.ijbiomac.2016.08.058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structural properties and the inhibition on alpha-D-glucosidase activity of the low molecular weight (LCMPs-II) obtained from the optimized acid hydrolysis of the Cordyceps militaris polysaccharides (CMPs) were investigated in this paper. The LCMPs-II with a molecular weight of 28 KDa mainly composed of rhamnose, xylose and glucose with the molar ratio of 1: 2.19: 6.73 was separated from LCMPs-I which was the acid hydrolysis product of CMPs by chromatography on Sephadex G-100 column. The solubility of LCMPs-II was tested to be 32.12 +/- 1.05 gin 100 mL distilled water under 25 degrees C. Its solubility was almost as twice as that of CMPs. Afterward, the structural features of LCMPs-II was investigated by a combination of chemical and instrumental analysis such as the specific rotation determination, FT-IR, periodate oxidation-Smith degradation, Congo-red, GC, scanning electron microscope and NMR. The results showed that the optical rotation of LCMPs-II was +25 degrees and it was 1,3-branched-rhamnoxyloglucan which had a linear backbone of (1 -> 4)-linked alpha-D-glucopyranose (alpha-D-Glcp units). (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 33
页数:7
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