Method and device of separating and extracting amino acid products from protein hydrolysates
A protein and amino acid technology, applied in chemical instruments and methods, preparation of organic compounds, preparation of sulfides, etc., can solve the problems of no separation and extraction, and achieve the effect of expanding separation, good separation effect and high yield
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Embodiment 1
[0031] Put 100 grams of pig blood powder protein into an 800mL round bottom flask, add 300mL of 6mol / L concentrated hydrochloric acid, heat to above 110°C, hydrolyze for 20 hours, collect the protein hydrolyzate, dilute it with water, let it flow through a 10cm, 15cm high, type I activated carbon adsorption chromatographic column with granular activated carbon body inside, then wash the chromatographic column with clean water, and use 0.1mol / L hydrochloric acid to prepare a mixed solution of ethanol hydrochloric acid with 50% ethanol concentration to flow through the column After the chromatographic column, wash the chromatographic column with clear water, combine the washing liquid after washing with the mixed solution of ethanol and hydrochloric acid to obtain the collected liquid, and recover the ethanol by distillation to obtain 150mL protein concentrate and 128mL ethanol with a volume percentage of less than 30%. solution, then use 2mol / L ammonia solution to adjust the pH ...
Embodiment 2
[0036]Put 100 grams of duck feathers in an 800mL round bottom flask, add 200mL of 10mol / L concentrated hydrochloric acid, heat to above 110°C, hydrolyze for 7 hours to collect the protein hydrolyzate, dilute it with water, let it flow through a 10cm diameter, 15cm high, type I activated carbon adsorption chromatographic column with granular activated carbon body inside, then wash the chromatographic column with clean water, and use 0.1mol / L hydrochloric acid to prepare a mixed solution of ethanol hydrochloric acid with 50% ethanol concentration to flow through the chromatographic layer After the column, wash the chromatographic column with water, combine the washing liquid and the washing liquid after washing with the mixed solution of ethanol hydrochloric acid to obtain the collected liquid, and recover the ethanol by distillation to obtain a 150mL protein concentrate, and then adjust the protein with 2mol / L ammonia solution. The pH value of the concentrated solution reaches 5...
Embodiment 3
[0039] Put 100 grams of unpeeled rapeseed cake in an 800mL round bottom flask, add 300mL of water to soak for 6 hours, and grind it into a paste, collect the rapeseed cake slurry, adjust the pH value to 7.0, and add 500 units / mL of bacteria Protease was hydrolyzed at 40°C for 3 hours, heated to 100°C and kept for 0.5 hours to inactivate the enzyme, adjusted the pH to 5.0, added 400 units / mL mycoprotease, hydrolyzed at 32°C for 3 hours, raised to 100°C and maintained for 0.5 hours to inactivate the enzyme; Then add 50 units / mL papain and hydrolyze at 31°C for 3 hours, raise the temperature to 100°C and keep it for 0.5 hours to inactivate the enzyme; then add 400 units / mL mycoprotease and hydrolyze at 32°C for 3 hours, filter with Buchner funnel to completely inactivate the enzyme , to obtain the amino acid mixed solution generated by enzymatic hydrolysis; adjust the pH value to 2.5 with 0.1mol / L hydrochloric acid, let it flow through a type I activated carbon adsorption chromato...
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