Preparation method of sleeve-fish skin low-molecular-weight collagen peptide
A technology of collagen peptide and low molecular weight, which is applied in the field of preparation of squid skin low molecular weight collagen peptide, can solve the problems of long preparation cycle, low protein extraction rate, difficult control of collagen molecular weight, etc., and achieve simple preparation method and uniform color , Increase the effect of added value
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0027] Take 1Kg of squid skin after washing and mash it with a masher; add 30L of NaOH solution with a mass fraction of 0.4% to the mashed squid skin, wash with water after soaking for 24h until the pH is neutral, then add 40L volume percent 12% n-butanol solution, stirred for 24 hours, washed with water until the pH was neutral and drained; 60L of citric acid solution with a mass fraction of 0.5% was added to the drained squid skin, heated to 60°C, and Constantly stirring and extracting for 7 hours, after filtration, the crude collagen extract was obtained; the pH of the crude collagen extract was adjusted to 8 with phosphate buffer, and then the compound enzyme was added. For the amount of the compound enzyme and the percentage content of each enzyme in the compound enzyme, see Table 1. Enzymolysis was carried out at an ultrasonic frequency of 40kHz, power of 100W, and temperature of 60°C for 2 hours; the obtained enzymolysis solution was heated to 95°C and kept for 7 minutes...
Embodiment 2
[0033]Take 1Kg of squid skin after washing and mash it with a masher; add 50L of NaOH solution with a mass fraction of 0.2% to the mashed squid skin, soak it for 30h, wash it with water until the pH is neutral, and then add 30L volume percent 10% n-butanol solution, stirred for 16 hours, washed with water until the pH is neutral and drained; 80L of 0.3% acetic acid solution was added to the drained squid skin, heated to 90°C, and continuously Stir and extract for 8 hours, and obtain the crude collagen extract after filtering; adjust the pH of the crude collagen extract to 7 with phosphate buffer, then add the compound enzyme, the amount of the compound enzyme added and the percentage content of each enzyme in the compound enzyme are shown in the table 1. Carry out enzymatic hydrolysis at an ultrasonic frequency of 30kHz, a power of 300W, and a temperature of 55°C for 1 hour; heat the obtained enzymatic solution to 90°C and keep it for 5 minutes to inactivate the enzyme. The fi...
Embodiment 3
[0039] Take 1Kg of squid skin after washing and mash it with a masher; add 35L of KOH solution with a mass fraction of 0.5% to the mashed squid skin, soak it for 28h, wash it with water until the pH is neutral, and then add 50L volume percent 15% n-butanol solution, stirred for 20 hours, washed with water until the pH is neutral and drained; 50L of citric acid solution with a mass fraction of 0.2% was added to the drained squid skin, heated to 80°C, and Constantly stirring and extracting for 6 hours, after filtration, the crude collagen extract was obtained; the pH of the crude collagen extract was adjusted to 7 with phosphate buffer solution, and then the compound enzyme was added. For the amount of the compound enzyme and the percentage content of each enzyme in the compound enzyme, see Table 1. Enzymolysis was carried out at an ultrasonic frequency of 25kHz, power of 400W, and temperature of 50°C for 1 hour; the obtained enzymolysis solution was heated to 100°C and kept for ...
PUM
Property | Measurement | Unit |
---|---|---|
quality score | aaaaa | aaaaa |
quality score | aaaaa | aaaaa |
quality score | aaaaa | aaaaa |
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