Production method of quinoa polysaccharides and polypeptides
The technology of a quinoa polysaccharide and a production method, which is applied in the field of quinoa polysaccharide polypeptide production, can solve the problems of difficult removal of small-molecule impurities, affecting the efficiency of enzymatic hydrolysis, and low yield of polypeptides, and achieves the effects of increasing protein yield and improving nutritional value.
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Embodiment 1
[0033] (1) Alkaline extraction of quinoa protein
[0034] Wash 3.8kg of quinoa, beat through a 100-mesh sieve, add water until the ratio of solid to liquid is 1:11.5, use 27°C, pH11 for 2 hours of leaching, centrifuge, and continue to produce starch in solid phase to obtain 1.86kg of starch , the liquid phase is clarified by ceramic membranes. Alkaline-extracted protein accounts for 70% of the total protein of quinoa according to Kjeldahl nitrogen determination, and the ceramic membrane flux is 80-120L / m 2 h.
[0035] (2) Amylase treatment
[0036] Adjust the pH of the ceramic membrane clarified solution to 6.4, heat to 50°C, and add 19g of medium-temperature α-amylase for enzymatic hydrolysis for 2 hours.
[0037] (3) Ultrafiltration membrane treatment
[0038] The amylase hydrolyzate was subjected to 5000 ultrafiltration membrane treatment. Both the retentate and the permeate were subjected to Kjeldahl nitrogen determination to obtain a protein retention rate of 85% and...
Embodiment 2
[0046] (1) Alkaline extraction of quinoa protein
[0047]Wash 3.8kg of quinoa, beat through a 100-mesh sieve, add water until the ratio of solid to liquid is 1:12, use 35°C, pH11 to extract for 3 hours, centrifuge, and continue to produce starch in solid phase to obtain 1.91kg of starch , the liquid phase is clarified by ceramic membranes. The protein extraction rate calculated by Kjeldahl nitrogen determination is 81.96%, and the ceramic membrane flux is 80-120L / ㎡·h.
[0048] (2) Amylase treatment
[0049] The ceramic membrane clarified solution was adjusted to pH 7, heated to 60° C., and 25 g of medium-temperature α-amylase was added for enzymatic hydrolysis for 2 hours.
[0050] (3) Ultrafiltration membrane treatment
[0051] The amylase hydrolyzate was subjected to 5000 ultrafiltration membrane treatment. Protein retention rate 90%, membrane flux 6.4-10.7L / m 2 h.
[0052] (4) Protease hydrolysis
[0053] Adjust the pH of the 5000 ultrafiltration membrane retentate t...
Embodiment 3
[0060] Embodiment 3: the influence of alkali extraction condition
[0061] Alkaline extraction of quinoa protein by changing step (1) in Example 2: the alkaline extraction conditions are shown in Table 2, and other conditions are the same as in Example 1.
[0062] Table 2 Effects of different alkaline extraction conditions on the extraction rate of starch and protein
[0063]
[0064] Embodiment 3: the influence of ultrafiltration membrane
[0065] Referring to step (3) ultrafiltration membrane treatment in Example 1: ultrafiltration membranes with different molecular weights are used for treatment, and the obtained data are shown in Table 4. Ultrafiltration can remove the small molecular impurities in the alkali extraction supernatant, which account for 80% of the protein quality of the alkali extraction, including reducing sugar and dextrin produced by hydrolyzing starch, and purify the protein and polysaccharide retained in the retentate. The inventors have found throu...
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