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中国精品科技期刊2020
付雪媛,杜芬,孙呈浩,等. 蛤蜊肽的制备工艺优化及其增强免疫活性[J]. 食品工业科技,2023,44(9):244−253. doi: 10.13386/j.issn1002-0306.2022080126.
引用本文: 付雪媛,杜芬,孙呈浩,等. 蛤蜊肽的制备工艺优化及其增强免疫活性[J]. 食品工业科技,2023,44(9):244−253. doi: 10.13386/j.issn1002-0306.2022080126.
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.
Citation: 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.

蛤蜊肽的制备工艺优化及其增强免疫活性

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

  • 摘要: 目的:以菲律宾蛤仔(Ruditapes philippinarum)为原料,研究蛋白肽制备工艺及其增强免疫活性。方法:以蛋白水解度为评价指标,筛选最适蛋白酶,采用单因素实验和响应面试验确定最佳酶解条件;氨基酸分析仪分析蛤蜊肽氨基酸组成;通过小鼠器官/体重比值、小鼠脾淋巴细胞转化实验、血清溶血素实验、小鼠腹腔巨噬细胞吞噬鸡红细胞实验、NK细胞活性实验评价蛤蜊肽的增强免疫活性。结果:菲律宾蛤仔蛋白肽制备的最适蛋白酶为胰蛋白酶,最佳酶解条件为温度48.4 ℃,pH8.0,加酶量3795 U/g,料液比1:2,水解时间4 h,该工艺下蛋白水解度达到15.33%,蛋白肽重均分子量为418 Da;其氨基酸组成合理,必需氨基酸占比达到41.48%;经口给予小鼠不同剂量的蛤蜊肽30 d,与空白对照组比较,小鼠的脏器比值无显著影响(P>0.05),低剂量(700 mg/(kg·d))与高剂量(2800 mg/(kg·d))下能显著提高血清溶血素水平(P<0.05),低剂量(700 mg/(kg·d))与中剂量(1400 mg/(kg·d))下能显著提高小鼠腹腔巨噬细胞吞噬鸡红细胞吞噬率(P<0.01),具有较好的增强免疫活性。结论:该方法下制备的蛤蜊肽水解程度较高、分子量低且分布集中,并具有一定增强免疫活性,具有开发成保健食品或特殊膳食食品的潜能。

     

    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.

     

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