Abstract
Polysaccharides in plants and microorganisms have important application value, and their purification and preparation is a prerequisite for in-depth research. However, there is currently a lack of dedicated separation and purification instruments for polysaccharide substances. In our previous work, a polysaccharide purification instrument (PSPI) was designed using post-column split-flow and post-column derivatization schemes and developed. In this study, the PSPI was applied to separation and preparation of the soybean soluble polysaccharides (SSPSs) and obtained the purified SSPS (SSPS-P). The total carbohydrate content in SSPS-P reached 97.2%, compared to 81.7% in SSPS, and the carbohydrate recovery rate was 86.5%. The composition and structure of SSPS-P have been assessed by HPLC, FT-IR, and NMR. SSPS-P was a polysaccharide with a molecular weight (M(w)) of 354 KDa, composed of D-glc, D-gal and L-ara with the molar ratio of 0.02:2.08:1.01. The structure of SSPS-P was mainly →4)-β-galp-(1→unit. The α-L-araf residues were also detected in the form of T-α-L-araf-(1→2)-α-L-araf-(1→, →3)-α-L-araf-(1→ and →3,5)-α-araf-(1→. PSPI could be applied for rapid and precise separation and preparation of polysaccharides.