Table 1e.
Separation and purification of by AEC and GFC.
| Anion exchange chromatography(AEC) | Gel filtration chromatography(GFC) | |
|---|---|---|
| Principle | Polysaccharides are separated according to charge and polarity indices | Fractional distillation according to polysaccharide size and shape |
| Elution order | ① Acidic polysaccharides with high uronic acid content could strongly bind to anion resin, while neutral polysaccharides had no interaction with anion resin, so they were eluted first. ② Fractionation is performed by using a combination of gradient elution practices and different ionic eluents |
① Macromolecules and high molecular weight polysaccharides do not enter the pores of the gel and are first eluted; ② Polysaccharides with small and low molecular weights block the pores of the gel and are finally eluted. |
| Chromatographic column | Diethylaminoethyl(DEAE) | Agarose, agar propylene, Superdex, biogel and agarose |
| Anion exchanger/Gel selection | Depends on small-scale experiments and the concentration of uronic acid in the polysaccharide | Much depends on the nature and source of the polysaccharide to be fractionated |
| limitation | Long time consuming; According to different uses, different resins need to be selected, and the general scope of application is small. | Instruments are expensive, inefficient, lack automation and difficult to scale up. |