Method for preparing avenin ACE inhibiting peptide
A technology of oat protein and inhibitory peptides, which is applied in the fields of cardiovascular system diseases, fermentation, drug combination, etc., can solve the problems of single variety, insufficient total output, and restricting the development of oat industry, etc., and achieve the effect of strong inhibitory peptide activity
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Embodiment 1
[0035] Take 15kg of oat bran that has been crushed and passed through a 40-mesh sieve, add 150L of water, stir and mix, heat to 45°C, adjust the pH to 4.5-5.0, add complex polysaccharide enzyme Viscozyme L 0.375L, enzymatic hydrolysis reaction for 2 hours, and heat up to 50°C , and adjust the pH to 9.5, continue to stir for 30min, centrifuge (3000r / min, 20min), collect the supernatant and adjust the pH to 4.5, centrifuge (3000r / min, 20min) to get 1.35kg of precipitate, add 27L of water and mix After homogenization, adjust the temperature and pH to 60°C and 7.5 respectively, add alkaline protease Alcalase 3.0T 18g to react for 90min, raise the temperature to 90°C, and keep it for 10min to inactivate the enzyme, after cooling to room temperature, centrifuge (3000r / min, 30min ) to obtain the supernatant, followed by ion-exchange chromatography, gel filtration chromatography and reversed-phase high-performance liquid chromatography for separation, and four peptide components with s...
Embodiment 2
[0037] Take 10kg of oat bran that has been crushed and passed through a 40-mesh sieve, add 100L of water, stir and mix well, heat to 40°C, adjust the pH to 4.5-5.0, add 0.25L of complex polysaccharide enzyme Viscozyme L, enzymatic hydrolysis reaction for 2 hours, and heat up to 50°C , and adjust the pH to 9.5, continue to stir for 30min and then centrifuge (3000r / min, 20min), collect the supernatant and adjust the pH to 4.5, centrifuge (3000r / min, 20min) to obtain a precipitate of 0.9kg, add 18L of water to mix After homogenization, adjust the temperature and pH to 60°C and 7.5 respectively, add alkaline protease Alcalase 3.0T 12g to react for 90min, raise the temperature to 90°C, and keep it for 10min to kill the enzyme, after cooling to room temperature, centrifuge (3000r / min, 30min ), to obtain the supernatant, which was separated by ion-exchange chromatography, gel filtration chromatography and reversed-phase high-performance liquid chromatography in sequence, and four pept...
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