Preparation method and application of rapeseed cake source metal chelating peptide and peptide metal chelating compound
A metal chelating peptide and rapeseed cake technology, which is applied in the preparation method of peptides, chemical instruments and methods, peptides, etc., can solve the problems of adverse effects on growth and development, affecting the synthesis and transformation of DNA polymerase, and achieve the goal of slowing down aging Effect
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Embodiment 1
[0026] The rapeseed cake was pulverized by using a high-speed pulverizer, 500 g of raw material was taken, 3 L of 75% (volume percentage) ethanol aqueous solution was added, stirred and soaked for 24 hours, and the liquid was changed every 6 hours during this period. After filtering, the precipitate was washed with 3L of water and then filtered, and after drying, a light brown crude rapeseed protein was obtained. The average yield of crude protein was 21.46%.
Embodiment 2
[0028] Take 4g of rapeseed crude protein, add 100ml of deionized water, adjust the pH to 8.0 with 1mol / L NaOH solution, add 0.08g of Alcalase enzyme, and carry out the enzymatic hydrolysis reaction of the reaction mixture at 55°C, during which 1mol / L L of NaOH solution was used to adjust the pH to maintain the reaction system at a pH of 8.0. When the reaction time reaches 4 hours, put the reaction solution in a boiling water bath to inactivate the enzyme, then put the protein hydrolyzate in a pressure cooker, and treat it under high pressure at 121° C. for 10 minutes to obtain a hydrolyzate.
[0029] The obtained high-pressure treatment hydrolyzate is subjected to freeze-drying treatment to obtain crude metal chelating peptide powder. The degree of hydrolysis of the hydrolyzate was 22.31% when detected by TNBS method for 4 hours. When the peptide concentration was 5 mg / ml, its Zn was detected by EDTA titration 2+ The average chelation rate is 84.36%.
Embodiment 3
[0031] Take 4g of rapeseed crude protein, add 100ml of deionized water, adjust the pH to 7.0 with 1mol / L NaOH solution, add 0.08g of papain, and carry out the enzymatic hydrolysis reaction of the reaction mixture at 60°C, during which 1mol / L L of NaOH solution was used to adjust the pH to maintain the reaction system at a pH of 7.0. When the reaction time reaches 1 hour, put the hydrolyzate in boiling water and inactivate the enzyme for 10 minutes.
[0032] The obtained hydrolyzate is freeze-dried to obtain crude metal chelating peptide powder. The degree of hydrolysis of the hydrolyzate was 20.82% when detected by TNBS method for 1 hour. When the peptide concentration was 5 mg / ml, its Zn was detected by EDTA titration 2+ The average chelation rate is 29.79%.
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