Method of using coconut cake globulin as raw material to prepare ACE inhibiting peptide
A technology of globulin and inhibitory peptides, which is applied in the field of preparation of coconut bran globulin, ACE inhibitory peptides, and preparation of ACE inhibitory peptides, can solve the problems of waste of resources, active ingredients such as proteins have not been developed and utilized, and achieve the effect of promoting development
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Embodiment 1
[0024] 1. Pre-treatment of raw materials Select mature old coconut fruits, then remove the shells, peel off the seed coat, wash, grate, and squeeze the juice to obtain coconut bran. Coconut bran is dried at 45°C, crushed, passed through a 60-mesh sieve, and then petroleum ether or ether is added at a ratio of 1:10 (m / v) to extract the remaining coconut oil to obtain defatted coconut bran powder.
[0025] 2. To extract globulin, add 0.4mol / L sodium chloride solution to the defatted coconut bran powder at a ratio of 1:10 (m / v), shake and extract at room temperature for 2 hours, filter, and collect the filtrate. Add the above-mentioned sodium chloride solution (1:10, m / v) to the filter residue again, repeat the extraction 3 times according to the above method, and combine the collected filtrates. The filtrate was centrifuged at 4° C. and 12000 rpm for 15 min, and the supernatant was collected. Put this supernatant into a dialysis membrane with a molecular weight cut off of 8000,...
Embodiment 2
[0031] 1. Pre-treatment of raw materials Select mature old coconut fruits, then remove the shells, peel off the seed coat, wash, grate, and squeeze the juice to obtain coconut bran. Coconut bran is dried at 50°C, crushed, passed through a 60-mesh sieve, and then petroleum ether or ether is added at a ratio of 1:15 (m / v) to extract the remaining coconut oil to obtain defatted coconut bran powder.
[0032] 2. To extract globulin, add 0.4mol / L sodium chloride solution to the defatted coconut bran powder at a ratio of 1:10 (m / v), shake and extract at room temperature for 3 hours, filter, and collect the filtrate. Add the above-mentioned sodium chloride solution (1:15, m / v) to the filter residue again, repeat the extraction 3 times according to the above method, and combine the collected filtrates. The filtrate was centrifuged at 4° C. and 10000 rpm for 20 min, and the supernatant was collected. Put the supernatant into a dialysis membrane with a molecular weight cut-off of 8000, ...
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