Processing technology of composite freeze-dried powder of sex glands of apostichopus ja ponicus
A processing technology and freeze-dried powder technology, which is applied in the processing technology field of A. japonicus gonadal compound freeze-dried powder, can solve the problem that the supporting technology of A. japonicus industrial industry is not yet mature, the deep-processing of sea cucumber is in its infancy, and there is not much research on comprehensive utilization. and other problems, to achieve the effect of improving extraction rate and bioavailability, increasing microbial fermentation links, and reducing pollution
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Embodiment 1
[0020] The present embodiment provides the processing technology of japonicus gonad compound freeze-dried powder, comprising the following steps:
[0021] (1) Preliminary enzymatic hydrolysis: Beat the gonads of sea cucumbers, then add compound protease, the enzyme addition amount is 0.5mKat / g, and the enzymatic hydrolysis time is 6h. After the enzymatic hydrolysis, the temperature is raised to kill the enzyme. Adjust the pH to 7.1.
[0022] There are many kinds of proteins in the gonads of sea cucumbers, and the one-time enzymatic hydrolysis is not thorough, resulting in waste. Firstly, the present invention uses complex proteases to enzymolyze them initially, and partially enzymolyzes the proteins with large molecular weights.
[0023] (2) Acid hydrolysis: add an organic acid, the weight of the added organic acid is 5% of the weight of the sea cucumber gonad, and maintain at 40°C for 3 hours. The function of adding organic acid is mainly to further release the protein in th...
Embodiment 2
[0032] Example 2 Determination of Polypeptide Content in Enzymolysis Supernatant
[0033] The determination of the peptide content in the enzymatic hydrolyzate was carried out with reference to the literature (Lu Wei, Ren Guopu, Song Junmei. Determination method of peptide content in protein hydrolyzate[J]. Food Science, 2005,26(7):169-171), Gly -Gly-Tyr-Arg standard products are configured into 0.0, 0.2, 0.4, 0.6, 0.8, 1.0, 1.2, 1.4, 1.6 and 1.8mg / ml standard solutions, respectively take 6ml of the standard solution into a 10ml centrifuge tube, add double shrinkage 2.4ml of urea reagent A and 1.6ml of biuret reagent B, mix well. Let it stand for 10 minutes, centrifuge at 2000r / min for 10 minutes, take the supernatant after centrifugation and measure the OD value under a 540nm spectrophotometer, draw the standard curve with the peptide concentration as the abscissa and the OD value as the ordinate, and the peptide content in the sample is passed The regression equation is cal...
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