Process for preparing red alga oligose
A technology of red algae oligosaccharide and red algae polysaccharide, applied in oligosaccharide and other directions, can solve the problems of serious oxidation degree of products, unsuitable for industrial production, difficult separation and purification, etc., and achieves inhibition of Bacillus subtilis growth, low price, and optimized process. effect of steps
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Embodiment 1
[0023] Weigh 40g of κ-carrageenan and add it to 2 liters of water, boil it to make it into a sol, treat the 732-type cation exchange resin with hydrochloric acid, and wash it until neutral, take 420g and add it to the carrageenan sol, and stir in a water bath at 90°C for reaction After reacting for 6 hours, the solid cation exchange resin was removed by suction filtration; neutral activated carbon with a particle size of 50 mesh was installed in a 6×60 cm chromatographic column, and the solution after suction filtration was directly adsorbed on the chromatographic column, and the solution could be repeatedly adsorbed twice. The second time, the adsorption speed is 5ml / min and 10ml / min respectively, after all the adsorption, wash with water, first remove the small molecular impurities and monosaccharide part, and then elute with 8% ethanol solution to obtain The eluate of oligosaccharides (2 sugars) was eluted with a concentration of 15% ethanol solution to obtain an eluate of o...
Embodiment 2
[0025] Weigh 40g of λ-carrageenan and add it to 2 liters of water, boil it to make it into a sol; treat the 732-type cation exchange resin with sulfuric acid, and wash it until neutral, take 420g and add it to the carrageenan sol; stir and react in a water bath at 90°C, After reacting for 6 hours, remove the solid cation exchange resin by suction filtration; put the neutral activated carbon with a particle size of 50 mesh in a 6×60cm chromatographic column, and the solution after suction filtration is directly adsorbed on the chromatographic column, and the solution can be repeatedly adsorbed twice , the adsorption speed is 5ml / min and 10ml / min respectively, after all the adsorption, wash with water, firstly remove the small molecular impurities and monosaccharide part, then elute with the concentration of 8% ethanol solution to obtain the polysaccharide with a degree of polymerization of 2 The eluate of oligosaccharides (2 sugars) was eluted with a concentration of 15% ethanol...
Embodiment 3
[0027] Weigh 40g of agar gel and add it to 2 liters of water, boil it to make it into a sol, treat the 732-type cation exchange resin with hydrochloric acid, and wash it until neutral, take 420g and add it to the agar sol; stir and react in a water bath at 90°C for 6 hours Finally, the solid cation exchange resin was removed by suction filtration; the neutral activated carbon with a particle size of 50 mesh was installed in a 6×60cm chromatographic column, and the solution after suction filtration was directly adsorbed on the chromatographic column, and the solution could be repeatedly adsorbed twice. The speeds are 5ml / min and 10ml / min respectively. After all the adsorption, wash with water to remove small molecular impurities and monosaccharides, and then elute with 8% ethanol solution to obtain oligosaccharides with a degree of polymerization of 2. The eluate of sugar (2 sugars) was eluted with a concentration of 15% ethanol solution to obtain an eluate of oligosaccharides (...
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