Clean chitin production process with physical separation and biological enzymolysis
A technology of clean production and physical separation, applied in the field of chitin processing, can solve the problems of low purity of chitin, large amount of enzyme, uneconomical and other problems
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Embodiment 1
[0020] First add 100kg of fresh shrimp and crab shells to the extrusion device, extrude and remove biomass such as protein and fat in the crab shells, and then add 0.5kg A.S1.398 Bacillus subtilis neutral protease (purchased from Wuxi Enzyme Preparation Factory, Activity 50000u / g, optimum temperature 40°C, optimum pH 7.2) and 2.5kg water diluted protease aqueous solution, enzymatic hydrolysis for 2h to 3h.
[0021] After the enzymatic hydrolysis, filter out the proteolysis solution, and the solid matter is the shrimp and crab shells after the protein has been removed.
[0022] Add 3 times the weight of aqueous hydrochloric acid solution with a concentration of 5wt% to the solid to soak for 6-8 hours, wash and drain.
[0023] Add 1.5 times the weight of 8wt% lye (can be sodium hydroxide aqueous solution or potassium hydroxide aqueous solution) to the drained solid, and heat the mixture to 90-95°C for 1.0 ~1.5 h, and then keep warm for 4~5 hours to take out the solid matter....
Embodiment 2
[0027] Add 100kg of fresh shrimp and crab shells into the extrusion device, and squeeze and remove biomass such as protein and fat in the crab shells. Dilute the protease aqueous solution formed with 0.5kg trypsin (purchased from Hangzhou Sanye Biochemical Factory, activity 4000u / g, optimum temperature 40°C, optimum pH 7.5~8) and 1.5kg water. Mix the above-extruded shrimp and crab shells with a protease aqueous solution, and enzymatically hydrolyze the protein in the extruded fresh shrimp and crab shells for 3 hours to 4 hours.
[0028] After the enzymatic hydrolysis, filter out the proteolysis solution, and the solid matter is the shrimp and crab shells after the protein has been removed.
[0029] Add 2 times the weight of aqueous hydrochloric acid solution with a concentration of 3wt% to the solid to soak for 6-8 hours, wash and drain.
[0030] Add 2 times the weight of 5wt% lye (can be sodium hydroxide aqueous solution or potassium hydroxide aqueous solution) to the dra...
Embodiment 3
[0034] Add 100kg of fresh shrimp and crab shells into the extrusion device, and squeeze and remove biomass such as protein and fat in the crab shells.
[0035] 0.35kg A.S1.398 Bacillus subtilis neutral protease (purchased from Wuxi Enzyme Preparation Factory, activity 50000u / g, optimum temperature 40°C, optimum pH 7.2) and 0.15kg trypsin (purchased from Hangzhou Sanye Biology Chemical plant, activity 4000u / g, optimal temperature 40°C, optimal pH 7.5~8) with 2~3 times of water, and then add the extruded shrimp and crab shells above, enzymatic hydrolysis time 2h~3h.
[0036] The protein in fresh shrimp and crab shells after compound enzymatic hydrolysis and extrusion, trypsin has a good effect, but the price is more expensive. It is combined with the cheaper A.S1.398 Bacillus subtilis neutral protease, and the two proteases are mixed together to enzymatically Solve the shrimp and crab shells after the above pretreatment.
[0037] After the compound enzyme enzymatic hydrolysis i...
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