首页 | 本学科首页   官方微博 | 高级检索  
     

半叶马尾藻多糖的分离纯化与光谱分析
引用本文:宋云端,孟庆勇,徐美奕. 半叶马尾藻多糖的分离纯化与光谱分析[J]. 中药材, 2007, 30(8): 951-954
作者姓名:宋云端  孟庆勇  徐美奕
作者单位:广东医学院分析中心,广东湛江,524023
摘    要:本文对半叶马尾藻多糖采用水提醇沉法粗提,蛋白酶联合Sevag法去蛋白纯化,凝胶过滤柱层析分离得半叶马尾藻纯多糖的不同组分,溴化钾压片红外光谱测定和紫外光谱扫描鉴定分析。结果表明,SHP的苯酚-硫酸呈色反应呈阳性,茚三酮反应呈弱阳性,碘-碘化钾反应呈阴性,说明提取物为非淀粉性多糖。SHP的提取率为8.56%,总糖含量为90.96%。凝胶过滤柱层析结果表明,半叶马尾藻多糖中含有吡喃多糖、木聚糖、半乳糖、阿拉伯糖、葡萄糖、鼠李糖和果糖等。紫外扫描结果显示多糖几乎不含核酸和蛋白质;红外光谱显示SHP主要为吡喃多糖,并显示多糖分子结构中存在β2糖苷键,还存在α-D-半乳吡喃糖的特征吸收峰。

关 键 词:半叶马尾藻多糖  提取  分离  纯化  光谱分析
文章编号:1001-4454(2007)08-0951-04
修稿时间:2007-01-04

Separation, Purification and Spectrum Analysis of SHP
SONG Yun-duan,MENG Qing-yong,XU Mei-yi. Separation, Purification and Spectrum Analysis of SHP[J]. Journal of Chinese medicinal materials, 2007, 30(8): 951-954
Authors:SONG Yun-duan  MENG Qing-yong  XU Mei-yi
Affiliation:Analysis Center of Guangdong Medical College, Zhanjiang 524023, China
Abstract:Crude SHP was obtained from extracting with hot water and precipitating with ethyl alcohol. Free proteins were removed by trypsinase combined with Sevage method. Different fractions were got by gel filtration chromatography. The molecule structure was analyzed by ultraviolet spectrum scanning and KBr infrared spectroscope. The results showed that the reaction of phenol-sulfuric acid was postiive, reaction of ninhydrin was weak positive and reaction of iodine-potassium iodide was negative, the extraction was regarded as a non-starch polysaccharide. Extraction rate of SHP was 8.56% and the content of polysaccharides was 90.96%. Gel filtration chromatography showed that SHP composed of furanopolysaccharides, xylose, galactose, arabinose, glucose, rhamnose and fructose. Ultraviolet spectrum showed that SHP contained little DNA and protein, infrared spectrum showed that SHP was main furanopolysaccharides and had beta-glycosidic bouds in its molecule structure, and there was a characteristic absorb peak of at-D-galactopyranosyl in it.
Keywords:SHP    Extract    Separate    Purify    Spectrum analyze
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号