| CPC A23L 33/18 (2016.08) [A23J 1/04 (2013.01); A23J 3/04 (2013.01); A23J 3/341 (2013.01); A23L 5/23 (2016.08); A23L 5/25 (2016.08); A23L 5/273 (2016.08); A23L 17/65 (2016.08); A61P 15/10 (2018.01); B01D 15/1871 (2013.01); B01D 15/327 (2013.01); B01D 15/362 (2013.01); B01D 21/262 (2013.01); B01D 71/02 (2013.01); C07K 1/18 (2013.01); C07K 1/20 (2013.01); C07K 1/36 (2013.01); C07K 14/43504 (2013.01); A23V 2002/00 (2013.01)] | 7 Claims |

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1. An oyster oligopeptide composition, wherein the oyster oligopeptide composition at least comprises peptide segments RI, IR and VR in its composition;
based on a mass of the oyster oligopeptide composition, a content of the RI is ≥3.60 mg/100 g, a content of the IR is ≥7.60 mg/100 g, and a content of the VR is ≥6.50 mg/100 g;
wherein the oyster oligopeptide composition is prepared as follows:
1) adding water to an oyster meat raw material to obtain a mixed material liquid, adding concentrated hydrochloric acid to the mixed material liquid and stirring, and collecting a precipitate after solid-liquid separation;
2) adding water to the precipitate to obtain a slurry, adding alkali to perform a protein denaturation treatment at 85-90° C., so as to obtain a denatured solution of oyster protein;
3) adding a neutral protease and a papain to the denatured solution of oyster protein, and performing enzymolysis treatment for 3-6 h, so as to obtain an enzymolysis solution after the neutral protease and the papain are inactivated;
4) centrifuging the enzymolysis solution to obtain a centrifugal supernatant, and then performing treatments of filtration and column chromatography on the centrifugal supernatant in sequence, so as to obtain the oyster oligopeptide composition.
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