Purification, characterization and enzymatic degradation of YCP, a polysaccharide from marine filamentous fungus Phoma herbarum YS4108

被引:123
作者
Yang, XB
Gao, XD [1 ]
Han, F
Xu, BS
Song, YC
Tan, RX
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, Nanjing 210009, Peoples R China
[2] Nanjing Univ, Inst Funct Biomol, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Peoples R China
关键词
YCP; Phoma herbarum; enzymatic modification; alpha-amylase; mitogenic activity;
D O I
10.1016/j.biochi.2005.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
YCP, a mitogenic polysaccharide with its molecular weight (MW) of 2.4 x 10(3) kDa, was isolated from the mycelium of the marine filamentous fungus Phoma herbarm YS4108 by a combination of ion-exchange chromatography on DEAE-32 and gel permeation over Sephacryl S-400. The detailed compositional, spectroscopic and methylation analyses of the polysaccharide demonstrated that its backbone possessed most likely a linear alpha-(1 --> 4) bonded glucopyranoside main chain co-bearing through side alpha-(1 --> 6)-linkage. The alpha-(1 --> 4) bondage of the glucopyranoside building blocks in YCP was confirmed by the observation that it could be hydrolyzed by the alpha-amylase produced by Bacillus licheniformis. A reliable concentration monitoring experimentation highlighted that the reducing sugars released continuously from YCP during its incubation with the enzyme, and the MW of the main resulting fragment weighed 0.8 x 10(4) Da with approximately 10% of YCP converted to maltose, maltotriose and glucose after a 120-min enzymatic degradation. Finally, YCP was found to be able to increase phagocytic activity of mice in vitro and in vivo, indicating that it may be looked up as a potent immunomodulator that could activate macrophages. (C) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:747 / 754
页数:8
相关论文
共 30 条
[1]
Regulation of phagosome maturation by signals from Toll-like receptors [J].
Blander, JM ;
Medzhitov, R .
SCIENCE, 2004, 304 (5673) :1014-1018
[2]
NEW METHOD FOR QUANTITATIVE-DETERMINATION OF URONIC ACIDS [J].
BLUMENKR.N ;
ASBOEHAN.G .
ANALYTICAL BIOCHEMISTRY, 1973, 54 (02) :484-489
[3]
(1->3)-beta-D-glucans as biological response modifiers: A review of structure-functional activity relationships [J].
Bohn, JA ;
BeMiller, JN .
CARBOHYDRATE POLYMERS, 1995, 28 (01) :3-14
[4]
Structural characterization of the water-extractable polysaccharides from Sophora subrostrata roots [J].
Dong, Q ;
Yao, J ;
Fang, JN .
CARBOHYDRATE POLYMERS, 2003, 54 (01) :13-19
[5]
Review: cyclodextrins and their interaction with amylolytic enzymes [J].
Hamilton, LM ;
Kelly, CT ;
Fogarty, WM .
ENZYME AND MICROBIAL TECHNOLOGY, 2000, 26 (08) :561-567
[6]
Kerekgyarto C, 1996, INT J IMMUNOPHARMACO, V18, P347, DOI 10.1016/S0192-0561(96)00038-0
[7]
POLYSACCHARIDES IN FUNGI .13. (1-]3)-ALPHA-D-GLUCAN FROM AN ALKALINE EXTRACT OF AGROCYBE-CYLINDRACEA, AND ANTITUMOR-ACTIVITY OF ITS O-(CARBOXYMETHYL)ATED DERIVATIVES [J].
KIHO, T ;
YOSHIDA, I ;
NAGAI, K ;
UKAI, S ;
HARA, C .
CARBOHYDRATE RESEARCH, 1989, 189 :273-279
[8]
KIHO T, 1987, CHEM PHARM BULL, V35, P4286
[9]
THE MURINE BONE-MARROW MACROPHAGE, A SENSITIVE INDICATOR CELL FOR MURINE MIGRATION-INHIBITORY FACTOR AND A NEW METHOD FOR THEIR HARVEST [J].
KLIMETZEK, V ;
REMOLD, HG .
CELLULAR IMMUNOLOGY, 1980, 53 (02) :257-266
[10]
Correlation between immunological activity, molar mass, and molecular structure of different (1->3)-beta-D-glucans [J].
Kulicke, WM ;
Lettau, AI ;
Thielking, H .
CARBOHYDRATE RESEARCH, 1997, 297 (02) :135-143