Optimization of Preparing Technology of Clam Peptide and Its Enhanced Immunomodulatory Effect

FU Xueyuan; DU Fen; SUN Chenghao; WANG Mingli; WANG Changwei

doi:10.13386/j.issn1002-0306.2022080126

Issue 9

May. 2023

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JOURNAL OF MECHANICAL ENGINEERING > 2023 > 44(9): 244-253.

FU Xueyuan, DU Fen, SUN Chenghao, et al. Optimization of Preparing Technology of Clam Peptide and Its Enhanced Immunomodulatory Effect[J]. Science and Technology of Food Industry, 2023, 44(9): 244−253. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022080126

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Optimization of Preparing Technology of Clam Peptide and Its Enhanced Immunomodulatory Effect

doi: 10.13386/j.issn1002-0306.2022080126

1.
Marine Biomedical Research Institute of Qingdao, Qingdao 266071, China
2.
Shanghai International Certification Assessment Services Co., Ltd., Shanghai 200030, China
3.
Penglai Huiyang Food Group Co., Ltd., Yantai 265609, China

Received Date: 15 Aug 2022
Issue Publish Date: 01 May 2023

Abstract

Abstract

Objective: Ruditapes philippinarum was used as raw material to investigate the preparation process of peptide and its enhanced immunomodulatory effect. Methods: The hydrolysis degree of protein was used as an evaluation index to screen the optimal protease. The single factor experiment and response surface test were used to determine the best enzymatic hydrolysis condition. The amino acid composition was analyzed using amino acid analyzer. And organ/body weight ratio, spleen lymphocyte transformation test, serum hemolysin experiment, peritoneal macrophage swallowing chicken red blood cell test, and NK cell activation experiment were used to assess the clam peptide enhanced immune activity. Results: Trypsin was the most suitable protease in the preparation of protein peptides from Ruditapes philippinarum. The optimal enzymatic conditions were temperature 48.4 ℃, pH8.0, enzyme concentration 3795 U/g, solid-liquid ratio 1:2, and hydrolysis time 4 hours. The average molecular weight of protein-peptide was 418 Da with 15.33% hydrolysis degree under optimal enzymatic conditions. The amino acid composition of the clam peptide was reasonable and the proportion of essential amino acids reached 41.48%. The organ ratio of BALB/c mice did not change significantly as compared to the control group after receiving various doses of oral clam peptides for 30 days. Furthermore, the serum hemolysin levels were significantly (P<0.05) increased of low dose (700 mg/(kg·d)) and high dose (2800 mg/(kg·d)) groups and the phagocytic rate of peritoneal macrophage swallowing chicken red blood cells was significantly (P<0.01) increased of low dose (700 mg/(kg·d)) and middle dose (1400 mg/(kg·d)) groups, which indicated the enhanced immunomodulatory effect of the clam peptide. Conclusions: The clam peptide produced using this process shows a high degree of hydrolysis, a low molecular weight, and a concentrated distribution with enhanced immune function. It has the potential to produce healthy foods or foods for special dietary uses.
- clam peptide,
- preparation technology,
- molecular weight,
- degree of hydrolysis,
- immunoenhancement effect

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References

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Optimization of Preparing Technology of Clam Peptide and Its Enhanced Immunomodulatory Effect

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