Chitosan oligosaccharide/chito-oligomer single enzymatic production process
A production process, chitosan oligosaccharide technology, applied in the field of specific enzymatic production technology of chitosan oligosaccharide/chitosan oligomer, can solve the problems that hinder the production, sales and application of chitosan oligosaccharide, and the molecular weight distribution of chitosan oligosaccharide products Uniformity, inconsistent physiological activity, etc., to achieve the effect of uniform size, relative size, and controllable quality
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Embodiment 1
[0013] 3% chitosan is dissolved in the acetic acid of 1% concentration, adjusts pH to 5.8 with saturated sodium bicarbonate solution, adds immobilized endo-chitosan enzyme preparation by 5U / g, and immobilized endo-chitosan enzyme preparation is obtained by Provided by the chitosan resource development and utilization project team of Jiangxi Normal University; the enzymolysis reaction temperature is 45°C, and the enzymolysis reaction time is 3 hours; the immobilized enzyme is recovered by sieve filtration, and the enzymolysis supernatant is obtained; Add 30% column volume of enzymolysis supernatant to the upper end of the weakly acidic cationic resin D155 chromatography column, 0-3mol / L ammonia water gradient elution, collect and use DNS (3,5-dinitrosalicylic acid) reagent to detect whether the eluate is Containing reducing sugar; the white precipitate formed by chitosan components with larger molecular weights that have not been degraded into chitosan oligosaccharides in the el...
Embodiment 2
[0015] 3% chitosan is dissolved in the acetic acid of 1% concentration, adjusts pH to 5.8 with saturated sodium bicarbonate solution, adds the endo-chitosan enzyme preparation of free state by 5U / g, the endo-chitosan enzyme preparation of free state is obtained by Provided by the chitosan resources development and utilization project team of Jiangxi Normal University; the enzymolysis reaction temperature is 45°C, and the enzymolysis reaction time is 3 hours; the free state enzyme is recovered by ultrafiltration membrane filtration, and the enzymolysis supernatant is obtained; Add 30% column volume enzymolysis supernatant to the upper end of macroporous weakly acidic cationic resin D155 chromatographic column, 0-3mol / L ammonia water gradient elution, collect and use DNS reagent to detect whether the eluate contains reducing sugar; The white precipitate formed by chitosan components with larger molecular weights degraded into chitooligosaccharides can be directly filtered and rec...
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