Peanut protein active polypeptide and method for making same
A technology for active polypeptide and peanut protein, which is applied in the field of biologically active polypeptide and its preparation, can solve the problems of low peptide yield, high production cost, side reactions, etc., and achieves the effects of good solubility, stability and good solubility
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Embodiment 1
[0019] Embodiment 1: The preparation process of peanut protein active polypeptide:
[0020] Peanut → low temperature oil extraction → crude oil refining → refined oil
[0021] ↓
[0022] Peanut soybean meal→ultrafine grinding→semi-skimmed protein powder→enzymolysis→separation→fermentation enzymolysis→separation→ultrafiltration→desalination→concentration→drying→peanut protein active polypeptide (finished product). The specific preparation process is:
[0023] 1. Raw material pretreatment: Peanut cake is super crushed, diluted with water, passed through a 150-350 mesh sieve to make powdered peanut protein, adjusted the pH value to slightly alkaline with alkali and adjusted the solution temperature to the optimum temperature for enzyme reaction, and then added compound Enzyme A is reacted, and then the peanut protein powder is further purified:
[0024] (1) Peanut protein powder→water soluble (1:15 is the weight ratio of powder to water)→alkaline extraction (use ...
Embodiment 2
[0030] Embodiment 2: Functional experiment of peanut protein active polypeptide
[0031] (1) Determination of hypertensive activity
[0032] Add 100ul sample to 100ul 0.05M borate buffer solution, the pH of the buffer solution is 8.5, including 0.3M Nacl, 25mU angiotensin-converting enzyme (ACE), preheat at 37°C for 9 minutes; add 150ul hippuryl histidyl Start the reaction with leucic acid (HHL), react at 37°C for 0.8h, add 250ul of 1M hydrochloric acid to terminate the reaction; then add 1.5ml of ethyl acetate to extract hippuric acid, vortex and mix and then centrifuge (2000g, 15min); absorb 1ml of ethyl acetate layer into another test tube, dried, redissolved in 3ml deionized water after cooling, and measured its absorbance value at 228nm.
[0033] ACE inhibitory activity (%)=(A a -A b ) / (A a -A c )*100%
[0034] where A a : optical density in the absence of inhibitor
[0035] A b : optical density in the presence of inhibitor and enzyme
[0036] A c : optical de...
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