Preparation method of plant protein derivative with physiological activity and nutrition supplementing function
A technology of plant protein and physiological activity, which is applied in the preparation method of peptides, chemical instruments and methods, organic chemistry, etc., and can solve the problems of little research on peptides
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0035] Example 1 The heat treatment of protein
[0036] Heat treatment can denature the protein and stretch the spherical structure, which is conducive to hydrolysis, but heat treatment may cause protein aggregation, and may also cause sulfhydryl-disulfide bond exchange to produce other forms of substances. Use differential scanning calorimetry (DSC) / non-reducing SDS-PAGE to analyze the degree of denaturation. On the premise of reaching the expected degree of denaturation, find the appropriate heating temperature and time to reduce the loss of disulfide bonds (determination of disulfide bonds content). DSC results show that the degree of denaturation of the protein solution can reach more than 90% when heated at 80°C for 20min; at 90°C for 5min; In addition, under these heat treatment conditions, there is almost no loss of protein disulfide bond content, so choose the best combination of temperature and time at 80°C for 20 minutes as heat treatment before protein enzymatic hy...
Embodiment 2
[0040] Embodiment 2 enzymatic hydrolysis method
[0041] 5% Glycinin solution after treatment, the temperature is controlled by circulating water bath at 60°C, the pH is controlled by a precision pH meter at 8.0±0.1 (during the hydrolysis process, 0.5M standard alkali is added dropwise to keep the pH constant), and 3% alkaline protease is hydrolyzed for 3 hours ; After alkaline protease hydrolysis, continue pepsin hydrolysis, adjust pH 2.0, control pH 2.0 ± 0.1 with a precision pH meter (during hydrolysis, add 0.5M hydrochloric acid to keep the pH constant), and control the temperature in a circulating water bath at 37 ℃, 2% pepsin hydrolysis for 2 hours, 5000g refrigerated centrifugation for 20 minutes, and the supernatant was obtained to obtain the desired crude peptide product. The degree of hydrolysis at the end of the hydrolysis process monitored by the pH-Stat method was about 20%.
Embodiment 3
[0042] The BH reduction method of embodiment 3 enzymolyzate
[0043] For the crude peptide product obtained in Example 2, add sodium borohydride (30% BH dissolved in 1M sodium hydroxide) to a final concentration of 1M, add 2 drops of octanol to defoam, react at 50°C for 30min, add concentrated hydrochloric acid ( to about pH2) to terminate the reaction and remove excess sodium borohydride and keep the system in a lower pH state to prevent oxidation of mercapto groups. The method of Example 5—4,4′-dithiodipyridine (4-DPS) method was used to quantitatively measure the sulfhydryl group and detect the reduction effect. Free thiols accounted for more than 95% of the total thiols.
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