Soybean protein enzymolysis method capable of reducing colour change
A soybean protease and protease technology, applied in the field of enzyme catalysis, can solve the problems of limited application, dark brown and even dark brown, etc., and achieve the effect of reducing production costs
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Embodiment 1
[0034] Embodiment 1 (comparative example)
[0035] Add 8g of soybean protein isolate (dry weight) and 200ml of tap water into an enzymolysis tank with a water jacket, and raise the temperature in the enzymolysis tank to 60°C under stirring. The pH value of the feed liquid in the enzymolysis tank was measured to be about 7.0 by a pH meter. Then, add 120 μ l Alcalase alkaline protease (2.4L, labeled activity is 2.4AU / gram, Danish NOVO company produces) and 0.48 gram Aspergillus niger acid protease (enzyme activity 3000u / g) in the enzymolysis tank, start under constant stirring enzymolysis. In this example, the substrate concentration is 40 grams of isolated soybean protein / liter of water, the ratio of Alcalase solution to the substrate is 15 μl / gram of isolated soybean protein, and Aspergillus niger acid protease accounts for 6% of the substrate (based on the dry weight of the substrate ), the total enzymatic hydrolysis time is 6 hours, the substrate degradation rate is about ...
Embodiment 2
[0036] Embodiment 2 (according to the present invention)
[0037] Repeat Example 1, but when adding Alcalase and Aspergillus niger acid protease in enzymolysis tank, add the hydrogen peroxide (being 30% hydrogen peroxide 4.8 milligrams) that is equivalent to 0.12 ‰ of soybean protein raw material dry basis weight wherein. The degradation rate of the substrate is still about 71%, and the degree of protein hydrolysis is still about 22%, but the color of the enzymolysis clear liquid is obviously lighter, and the discoloration inhibition rate reaches 29.3%.
Embodiment 3
[0038] Embodiment 3 (according to the present invention)
[0039] Repeat Example 2, but the added hydrogen peroxide is successively 0.06‰, 0.25‰, 0.50‰ and 1.9‰ of the dry basis weight of the soybean protein material. In these four cases, the substrate degradation rate and the degree of protein hydrolysis still remained at about 71% and 22%, but the color of the enzymolysis clear liquid became lighter with the increase of hydrogen peroxide addition, and the color change inhibition rate 25%, 32.4%, 35% and 51.8%, respectively. No residual hydrogen peroxide was detected in the enzymolysis solution with hydrogen peroxide addition of 1.9‰ by iodometric titration. It shows that hydrogen peroxide has been decomposed after high temperature inactivation at 95°C.
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