Method for preparing shellfish viscera fat by aqueous enzymatic method
A water enzymatic method and shellfish technology, applied in the field of preparation of shellfish viscera oil, can solve the problem that no one uses shellfish viscera oil, achieve the effects of reducing production costs, reducing dosage, and improving enzymatic hydrolysis efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
example 1
[0034] Fresh scallop viscera were taken, rinsed with 3% saline, drained, and frozen at -4°C for 48 hours, then taken out and thawed at 35°C for 0.5 hour. Place the frozen-thawed liquid of the scallop viscera after the above-mentioned freeze-thawing and crushing into a sterile enzymolysis tank, and perform autolysis at a temperature of 20°C. After 12 hours of autolysis, add 0.1% enzyme activity to 3.9×10 5 U / g of papain, the enzymolysis was continued for 3 hours at a pH of 7 and a temperature of 50°C. After heating the enzymolysis solution at 100°C for 10 minutes to inactivate the enzyme, add 2% (w / v) NaCl, then adjust the pH to 34 with 6mol / L hydrochloric acid solution, mix well and let it stand for 1 hour, then set aside at 2,000× Centrifuge for 30 min under the condition of g, and take the upper oil layer to obtain the scallop viscera fat.
[0035] Put the obtained scallop viscera fat into the extraction kettle of supercritical extraction equipment for extraction, and use s...
example 2
[0037] Fresh scallop viscera were taken, rinsed with 3% saline, drained, and frozen at -10°C for 12 hours, then taken out and thawed at 4°C for 5 hours. Place the frozen-thawed liquid of the scallop viscera after the above-mentioned freeze-thawed crushing into a sterile enzymatic hydrolysis tank, and perform autolysis at a temperature of 65°C. After autolysis for 3 hours, add 0.1% enzyme activity to 6×10 5 U / g of neutral protease, continue enzymatic hydrolysis for 4 hours at pH 7 and temperature 55°C. After heating the enzymolysis solution at 100°C for 10 minutes to inactivate the enzyme, add 5% (w / v) NaCl, then adjust the pH to 2 with 6mol / L hydrochloric acid solution, mix well and let it stand for 1 hour, then set aside at 2,000× Centrifuge for 30 min under the condition of g, and take the upper oil layer to obtain the scallop viscera fat.
[0038] Put the obtained scallop viscera fat into the extraction kettle of supercritical extraction equipment for extraction, and use s...
example 3
[0040] Fresh scallop viscera were taken, rinsed with 3% saline, drained, and frozen at -20°C for 12 hours, then taken out and thawed at 35°C for 1 hour. The scallop viscera after the freeze-thaw crushing was placed in a tray, irradiated with ultraviolet light for 10 minutes, added with 0.2mol / L KCl, and autolyzed for 6 hours at pH 6.0 and temperature 35°C. Adding 0.05% enzyme activity from the solution is 5.7×10 5U / g of trypsin, the enzymatic hydrolysis was continued for 1 hour at pH 8 and temperature 60°C. Heat the enzymolysis solution at 100°C for 10 minutes to inactivate the enzyme, add 10% (w / v) NaCl, then adjust the pH to 46 with 6mol / L hydrochloric acid solution, mix it and let it stand for 1 hour, then set aside at 2,000 Centrifuge for 30 min under the condition of ×g, and take the upper oil layer to obtain the scallop viscera fat.
[0041] Put the obtained scallop viscera fat into the extraction kettle of supercritical extraction equipment for extraction, and use sup...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com