Production method of low-salt oyster polypeptide and oligosaccharide nutrition powder
A production method and technology for oyster polypeptides, which are applied in the directions of fish protein composition, food hydrolysis, food science, etc., can solve the problems of underutilized value of oysters, difficult to achieve ideal effects, decreased protease activity, etc., to prevent The effect of serious sticking to the wall, shortening the cooling time and reducing energy consumption
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[0043] Example 1: Production of low-salt oyster polypeptide and oligosaccharide nutritional powder
[0044] (1) Desalting: Take 1kg of shelled oyster meat, add 4L of ice water and soak for 45min at 4℃, drain the water, add 4L of ice water and soak for 45min at 4℃, repeat 3 times.
[0045] (2) Sample sterilization and protein denaturation: homogenize the oyster meat after soaking and desalting, homogenize at 5000 rpm for 10 minutes, and place it in a water bath at 90°C for 10 minutes. The sample is sterilized and the protein is denatured.
[0046] (3) Sample cooling: add 2L of distilled water at 25°C to make the sample solution temperature 40.2°C, while diluting the sample solution, the pH of the sample solution is 6.58;
[0047] (4) High pH protease digestion: adjust the pH to 8.0 with 1mol / L NaOH, place the sample in a water bath set at 45℃, add 8g, 0.8% (w / w) trypsin to proteolysis 1.5 h, the pH of the sample solution is 7.2 at this time.
[0048] (5) Low pH protease enzymolysis: pl...
Example Embodiment
[0056] Example 2: Production of low-salt oyster polypeptide and oligosaccharide nutritional powder
[0057] (1) Desalting: Take 1kg of shelled oyster meat, add 6L of ice water, soak in 4℃ environment for 45min, drain the water, add 6L of ice water to soak for 45min, repeat 2 times.
[0058] (2) Sample sterilization and protein denaturation: Homogenize the oysters after soaking and desalting, homogenize at 5000 rpm for 10 minutes, and then place them in a water bath at 80°C for 15 minutes.
[0059] (3) Sample cooling: After high temperature treatment, add 1.5L of distilled water at 25℃, the temperature of the sample solution obtained is 46.7℃, and the sample solution is diluted.
[0060] (4) High pH protease enzymolysis: adjust the pH to 8.0 with 1mol / L NaOH, place the sample in a water bath with a temperature of 50℃, add 10g, 1.0% (w / w) alkaline protease to proteolysis 1h.
[0061] (5) Low pH protease enzymolysis: After high pH protease enzymolysis, the pH of the sample solution is no...
Example Embodiment
[0065] Example 3: Production of low-salt oyster polypeptide and oligosaccharide nutritional powder
[0066] (1) Desalting: Take 1kg of shelled oyster meat, add 2L of ice water, soak at 4℃ for 30min, drain the water, add 4L of ice water and soak for 30min at 4℃, repeat 6 times.
[0067] (2) Sample sterilization and protein denaturation: homogenize the oyster meat after soaking and desalting, homogenize it at 5000 rpm for 10 minutes, and place it in a water bath at 100°C for 10 minutes. The sample is sterilized and the protein is denatured.
[0068] (3) Sample cooling: Add 2L of distilled water at 28°C to make the temperature of the sample solution 55°C while diluting the sample solution. At this time, the pH of the sample solution is 6.58.
[0069] (4) High pH protease enzymolysis: adjust the pH to 8.0 with 1mol / L NaOH, place the sample in a water bath set at 55℃, add 8g, 0.8% (w / w) trypsin for proteolysis 1.5 h; At this time, the pH of the sample solution is 7.2.
[0070] (5) Low pH ...
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