摘要
对白子草中的多糖进行分离纯化,并对得到的多糖组分的理化性质进行分析。将脱脂后的白子草药材经热水提取,乙醇沉淀,木瓜蛋白酶-Sevag法去蛋白后,再经DEAE-SepharoseFastFlow离子交换柱色谱分离,透析除盐纯化得白子草多糖,采用高效液相色谱法,红外光谱和。H-NMR对其进行组成研究和分析。白子草多糖中的GDPs-2的纯度为87.3%,相对分子质量为2.03×10^4Da;GDPs.3的纯度为90.9%,相对分子质量为4.29×10^4Da。红外光谱无法确定GDPs-2是否有α构型的呋喃糖苷,但提示GDPs-3可能有α构型的呋喃糖苷键,1H-NMR分析初步判断GDPs-2和GDPs-3的糖苷键连接方式均为α型。GDPs-2由葡萄糖醛酸和木糖组成,摩尔比为1.1:0.63;GDPs-3由鼠李糖、葡萄糖醛酸、半乳糖、木糖和半乳糖醛酸组成,摩尔比为0.32:6.0:0.21:1.75:4.3。
The purpose of this study was to isolate and purify polysaccharide from C, ynura divaricata and analyze its monosaccharide composition. A water-soluble crude polysaccharide was obtained by hot water extraction, ethanol precipitation and deproteinization after degreasing. The crude polysaccharide then purified with DEAE-Sepharose Fast Flow column chromatography and dialysis. The mono- saccharide composition and structure were analyzed by HPLC, UV spectrophotometer and 1H-NMR. The results showed that the purity and molecular weight of GDPS-2 and GDPS-3 were 87. 3% , 2. 03 × 10^4 Da and 90. 9%, 4. 29 ×10^4 Da, respectively. The UV spectro- photometer and 1 H-NMR data suggested that glycosidic bond of GDPS-2 and GDPS-3 were α type. Both GDPs-2 and GDPs-3 were hom- ogeneous polysaccharides, and GDPs-2 was mainly composed of glucuronic acid and xylose at a molar ratio of 1.1 : 0. 63. GDPs-3 was mainly composed of rhamnose, glucuronic acid, galactose, xylose and galacturonic acid at a molar ratio of 0. 32: 6. 0: 0. 21: 1.75: 4. 3.
出处
《中国中药杂志》
CAS
CSCD
北大核心
2015年第8期1497-1502,共6页
China Journal of Chinese Materia Medica
基金
福建省自然科学基金项目(2012J01400)
关键词
白子草
白背三七
多糖
提纯
分离
结构分析
Gynura divaricata
polysaccharides
purification
monosaccharide composition