Composition with nutritional and moisturizing efficacies as well as preparation method and application of composition
A composition and efficacy technology, applied in the field of daily chemicals, can solve the problems of difficulty in controlling the molecular weight of degradation products, difficulty in obtaining active glucosamine, high price of specific enzymes, etc., achieve nutrition and moisturizing performance, and easy absorption , low-cost effect
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Embodiment 1
[0044] (1) with 2 mass parts chitosan (deacetylation degree is 92.0%, molecular weight 8 * 10 4 ) was dissolved in 200 parts by mass of 0.2mol / L, pH3 acetate buffer, 80 Hz ultrasonic wave for 15min, then added 0.005 parts by mass of lysozyme (Sigma-Aldrich, the same below), 0.005 parts by mass of cellulase (Sigma-Aldrich, The same below), reacted at 40°C for 4h; then added 0.0025 parts by mass of chitosanase (Sigma-Aldrich, the same below) and 0.0025 parts by mass of pectinase (Novozymes, Denmark, the same below), and reacted at 60°C 6h. The stirring state of 150rpm was maintained throughout the enzymolysis reaction. After the enzymolysis reaction was completed, the enzymolysis solution was heated at 95°C for 5 minutes to inactivate, then the temperature was lowered to 45°C, and 2 parts by mass of activated carbon was added. The decolorization time was 1 hour, and the activated carbon was filtered off. Finally, it was centrifuged at 3000 rpm, and the supernatant was taken to ...
Embodiment 2
[0050] (1) with 2 mass parts chitosan (deacetylation degree is 91.5%, molecular weight 12 * 10 4 ) was dissolved in 400 parts by mass of 0.2 mol / L acetate buffer solution with a pH of 5.5, ultrasonicated at 120 Hz for 45 minutes, then 0.1 parts by mass of lysozyme and 0.1 parts by mass of cellulase were added, and reacted at 55°C for 8 hours; then added 0.05 Parts by mass of chitosanase and 0.05 part by mass of pectinase were reacted at 70° C. for 12 hours. Stirring at 250rpm was maintained throughout the enzymolysis reaction. After the enzymolysis reaction, the enzymolysis solution was heated at 100°C for 10 minutes to inactivate it, then cooled to 55°C, and 4 parts by mass of activated carbon was added. The decolorization time was 2 hours, and the activated carbon was filtered off. Finally, it was centrifuged at a rotational speed of 5000 rpm, and the supernatant liquid was taken to obtain 350 parts by mass of an aqueous solution of glucosamine oligosaccharides with a chroma...
Embodiment 3
[0056] (1) with 2 mass parts chitosan (deacetylation degree is 92.7%, molecular weight 20 * 10 4 ) was dissolved in 300 parts by mass of 0.2 mol / L acetate buffer solution with a pH of 4.5, 100 Hz ultrasonic wave was used for 30 minutes, then 0.05 parts by mass of lysozyme and 0.05 parts by mass of cellulase were added, and the reaction was carried out at 50°C for 6 hours; then 0.0025 Parts by mass of chitosanase and 0.0025 parts by mass of pectinase were reacted at 65° C. for 8 hours. Stirring at 200rpm was maintained throughout the enzymolysis reaction. After the enzymolysis reaction, the enzymolysis solution was heated at 98°C for 8 minutes to inactivate, then cooled to 50°C, and 3 parts by mass of activated carbon was added. The decolorization time was 1.5h, and the activated carbon was filtered off. Finally, it was centrifuged at a rotational speed of 4500 rpm, and the supernatant was taken to obtain 250 parts by mass of an aqueous solution of glucosamine oligosaccharides ...
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