Structure and antitumor activity of extracellular polysaccharides from mycelium

被引:71
作者
Peng, YF
Zhang, L [1 ]
Zeng, FB
Xu, YX
机构
[1] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
[2] Huazhong Univ Sci & Technol, Coll Med, Wuhan 430030, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Ganoderma tsugae mycelium; extracellular polysaccharide; antitumor activity; conformation; light scattering;
D O I
10.1016/S0144-8617(03)00190-5
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two heteropolysaccharides coded as EPF1 and EPF2 were obtained from the crude extracellular polysaccharide (CEP) of Ganoderma tsugae mycelium by elution with DEAE-Sepharose CL-6B column. Their chemical structures and molecular mass were characterized by infrared, gas chromatography, C-13 NMR and size exclusion chromatography combined with laser light scattering (SEC-LLS). The results indicated that they were mainly composed with mannose, fucose, xylose, galactose and glucosamine. EPF2 was confirmed to be mainly a D-galacto-alpha-D-mannan. The weight-average molecular mass of the samples EPF1, EPF2 and CEP were 92.0 x 10(4), 8.35 x 10(4) and 23.8 x 10(4), respectively. The EPF1 existed as a compact coil chain in 0.2 M NaCl aqueous solution at 25 degreesC, while EPF2 as a flexible chain. The antitumor activities against Sarcoma 180 were tested both in vitro and in vivo. All the samples exhibited high inhibition ratio against Sarcoma 180 in mice, and the CEP has higher inhibition effect both in vivo and in vitro than EPF1 and EPF2. In view of these results, the presence of bound protein and mannose, and relatively expanded chain would be helpful to the enhancement of antitumor activities. This study suggested that the extracellular polysaccharides had a potential application as natural antitumor drugs. (C) 2003 Published by Elsevier Ltd.
引用
收藏
页码:297 / 303
页数:7
相关论文
共 27 条
[1]   CHANGE OF BIOLOGICAL-ACTIVITIES OF (1-]3)-BETA-D-GLUCAN FROM GRIFOLA-FRONDOSA UPON MOLECULAR-WEIGHT REDUCTION BY HEAT-TREATMENT [J].
ADACHI, Y ;
OHNO, N ;
OHSAWA, M ;
OIKAWA, S ;
YADOMAE, T .
CHEMICAL & PHARMACEUTICAL BULLETIN, 1990, 38 (02) :477-481
[2]  
CHIHARA G, 1969, Nature (London), V222, P687
[3]   COLORIMETRIC METHOD FOR DETERMINATION OF SUGARS AND RELATED SUBSTANCES [J].
DUBOIS, M ;
GILLES, KA ;
HAMILTON, JK ;
REBERS, PA ;
SMITH, F .
ANALYTICAL CHEMISTRY, 1956, 28 (03) :350-356
[4]   DETERMINATION OF DIETARY FIBER AS NONSTARCH POLYSACCHARIDES WITH GAS-LIQUID-CHROMATOGRAPHIC, HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC OR SPECTROPHOTOMETRIC MEASUREMENT OF CONSTITUENT SUGARS [J].
ENGLYST, HN ;
QUIGLEY, ME ;
HUDSON, GJ .
ANALYST, 1994, 119 (07) :1497-1509
[5]  
FAN QH, 2002, BIOCH ENG J, V10, P61
[6]  
Gorin P. A. J., 1981, ADV CARBOHYD CHEM BI, V38, P13, DOI [DOI 10.1016/S0065-2318(08)60309-1, 10.1016/S0065-2318(08)60309-1]
[7]   ASSIGNMENT OF C-13 SIGNALS IN NUCLEAR MAGNETIC-RESONANCE SPECTRA OF D-GALACTOPYRANO-ALPHA-D-MANNOPYRANANS FROM YEASTS [J].
GORIN, PAJ ;
MAZUREK, M .
CARBOHYDRATE RESEARCH, 1982, 105 (02) :283-287
[8]   CARBOXYMETHYLPACHYMARAN, A NEW WATER SOLUBLE POLYSACCHARIDE WITH MARKED ANTITUMOUR ACTIVITY [J].
HAMURO, J ;
YAMASHITA, Y ;
OHSAKA, Y ;
MAEDA, YY ;
CHIHARA, G .
NATURE, 1971, 233 (5320) :486-+
[9]   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
[10]   Prickly pear nopals pectin from Opuntia ficus-indica physico-chemical study in dilute and semi-dilute solutions [J].
Majdoub, H ;
Roudesli, S ;
Picton, L ;
Le Cerf, D ;
Muller, G ;
Grisel, M .
CARBOHYDRATE POLYMERS, 2001, 46 (01) :69-79