In this paper,Panax polysaccharides,including polysaccharides in Panax ginseng C.A.Meyer,Panax quinquefolius L.and Panax notoginseng were separated and purified,and the primary structure was studied.The optimal conditions of sevag was:sevag was added equivalent 1/4 volume of sugar,the volume ratio of chloroform and n-butanol was 5:1,repeated five times,and oscillation 25 min each time.The polysaccharides was deproteinized by method of sevag.Using sephadex G-100,five components were isolated and purified from polysaccharides in Panax ginseng C.A.Meyer,named PPG-1?PPG-2?PPG-3?PPG-4?PPG-5,whose relative molecular mass were 7×104?4×104?1.7×104?1×104?2×103;Five components were isolated and purified from polysa-ccharides named PPQ-1?PPQ-2?PPQ-3?PPQ-4?PPQ-5,whose relative molecular mass were 7.9×104?4.3×104?1.5×104?1.1×104?5.8×102,Two components were isolated and purified from polysaccharides in Panax notoginseng,whose relative molecular mass were 7×104?8.7×102.PPG-2?PPQ-1?PPQ-2?PPN-1 were considered a single component with a homogenous molecular Content ascertained by ultraviolet spectroscopy,sephadex G-100 and HPLC.Finding that the monosaccharide composition of these were mainly composed of glucose by analyzing the complete acid hydrolysates of PPG-2?PPQ-1?PPQ-2?PPN-1 by HPLC.Analyzing the results of the products from malaprade reaction and GC chromatogram of smith degradation products and IR,PPG-2 and PPQ-1 were mainly composed of ?-D-(1?4)or ?-D-(1?6)pyran glucose,both PPQ-2 and PPN-1 were glucan and mainly composed of?-D-(1?4)pyran glucose. |