目的以海藻海蒿子为原料制备褐藻糖胶,并对不同的提取、分离方法进行比较,对多糖的组成和结构进行初步分析。方法海蒿子脱脂干粉分别经水提取和酸提取以获得粗多糖,粗多糖分别经乙醇沉淀法和CaCl2沉淀法进行纯化。选取多糖组分F4用Q-Sep...目的以海藻海蒿子为原料制备褐藻糖胶,并对不同的提取、分离方法进行比较,对多糖的组成和结构进行初步分析。方法海蒿子脱脂干粉分别经水提取和酸提取以获得粗多糖,粗多糖分别经乙醇沉淀法和CaCl2沉淀法进行纯化。选取多糖组分F4用Q-Sepharose Fast Flow和Sephadex G-200凝胶柱进行分级分离,高效凝胶渗透色谱法(HPGPC)鉴定纯度及相对分子质量,气相色谱分析多糖的中性单糖组成。结果F4经分级分离得到3个级分:P1、P2和P3。P1、P2和P3均为均一组分,相对分子质量分别为:494400、61500和167600;P1由岩藻糖、木糖、甘露糖、葡萄糖和半乳糖构成,摩尔百分比43.4∶33.3∶6.2∶4.3∶12.8;P2由岩藻糖、木糖、甘露糖和半乳糖构成,摩尔百分比44.4∶15.1∶23.8∶16.7;P3由岩藻糖、木糖和半乳糖构成,摩尔百分比68.9∶3.7∶27.4。结论P1、P2和P3的单糖含量均以岩藻糖为主,但其他单糖组成有较大差别。展开更多
A series of oligomannuronates with series degree of polymerization（DP28） were prepared by acid hydrolysis from alginate-derived homopolymannuronate blocks, and the structures of the oligosaccharides were analyzed. T...A series of oligomannuronates with series degree of polymerization（DP28） were prepared by acid hydrolysis from alginate-derived homopolymannuronate blocks, and the structures of the oligosaccharides were analyzed. The macromolecule of alginate was treated by partial acid hydrolysis and fractionated at pH2.85 resulting in homopolymannuronate blocks. The homopolymer was degraded by acid hydrolysis, and the oligosaccharides were separated and purified by gel chromatography. The oligosaccharides were characterized by fluorophore-assisted carbohydrate electrophoresis（FACE）, and the structures of derived oligomannuronates were determined by ESI-MS, NMR as well as FTIR analysis.展开更多
文摘目的以海藻海蒿子为原料制备褐藻糖胶,并对不同的提取、分离方法进行比较,对多糖的组成和结构进行初步分析。方法海蒿子脱脂干粉分别经水提取和酸提取以获得粗多糖,粗多糖分别经乙醇沉淀法和CaCl2沉淀法进行纯化。选取多糖组分F4用Q-Sepharose Fast Flow和Sephadex G-200凝胶柱进行分级分离,高效凝胶渗透色谱法(HPGPC)鉴定纯度及相对分子质量,气相色谱分析多糖的中性单糖组成。结果F4经分级分离得到3个级分:P1、P2和P3。P1、P2和P3均为均一组分,相对分子质量分别为:494400、61500和167600;P1由岩藻糖、木糖、甘露糖、葡萄糖和半乳糖构成,摩尔百分比43.4∶33.3∶6.2∶4.3∶12.8;P2由岩藻糖、木糖、甘露糖和半乳糖构成,摩尔百分比44.4∶15.1∶23.8∶16.7;P3由岩藻糖、木糖和半乳糖构成,摩尔百分比68.9∶3.7∶27.4。结论P1、P2和P3的单糖含量均以岩藻糖为主,但其他单糖组成有较大差别。
文摘A series of oligomannuronates with series degree of polymerization（DP28） were prepared by acid hydrolysis from alginate-derived homopolymannuronate blocks, and the structures of the oligosaccharides were analyzed. The macromolecule of alginate was treated by partial acid hydrolysis and fractionated at pH2.85 resulting in homopolymannuronate blocks. The homopolymer was degraded by acid hydrolysis, and the oligosaccharides were separated and purified by gel chromatography. The oligosaccharides were characterized by fluorophore-assisted carbohydrate electrophoresis（FACE）, and the structures of derived oligomannuronates were determined by ESI-MS, NMR as well as FTIR analysis.
