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中国精品科技期刊2020
廖慧琦,曹少谦,杨华,等. 鲐鱼免疫活性肽的酶解工艺优化[J]. 食品工业科技,2022,43(14):163−170. doi: 10.13386/j.issn1002-0306.2021090087.
引用本文: 廖慧琦,曹少谦,杨华,等. 鲐鱼免疫活性肽的酶解工艺优化[J]. 食品工业科技,2022,43(14):163−170. doi: 10.13386/j.issn1002-0306.2021090087.
LIAO Huiqi, CAO Shaoqian, YANG Hua, et al. Optimization of Enzymatic Hydrolysis Process of Immune Active Peptide in Chub Mackerel[J]. Science and Technology of Food Industry, 2022, 43(14): 163−170. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021090087.
Citation: LIAO Huiqi, CAO Shaoqian, YANG Hua, et al. Optimization of Enzymatic Hydrolysis Process of Immune Active Peptide in Chub Mackerel[J]. Science and Technology of Food Industry, 2022, 43(14): 163−170. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021090087.

鲐鱼免疫活性肽的酶解工艺优化

Optimization of Enzymatic Hydrolysis Process of Immune Active Peptide in Chub Mackerel

  • 摘要: 为了优化鲐鱼免疫活性肽的酶法制备工艺,以水解度和小鼠脾淋巴细胞相对增殖率为指标,在单因素实验的基础上,选择酶添加量、酶解时间和酶解温度为考察因素,采用Box-Behnken法进行三因素三水平响应面试验设计,确定鲐鱼免疫活性肽的最佳酶解条件,并对得到的鲐鱼免疫活性肽进行氨基酸组成分析。结果表明,中性蛋白酶为最优蛋白酶,最佳酶解条件为酶添加量8800 U/g、时间7 h、温度52 ℃,验证实验发现在该条件下得到的酶解产物对小鼠脾淋巴细胞相对增殖率为48.11%±2.67%,与回归方程预测值相近。同时鲐鱼免疫活性肽氨基酸含量丰富,其中人体必需氨基酸达45.52%,疏水性氨基酸含量为32.00%。研究结果为鲐鱼免疫活性肽的酶法制备提供了理论依据,为进一步实现鲐鱼资源的高值化利用提供了参考。

     

    Abstract: In order to optimize the enzymatic extraction process of chub mackerel immune active peptide, taking the proliferation rate and degree of hydrolysis of mouse spleen lymphocytes as indicators, on the basis of single factor tests, the enzyme addition amount, enzymatic hydrolysis time and enzymatic hydrolysis temperature were selected as the investigation factors, and the Box-Behnken method was used for three factors and three levels response surface test design to determine the best enzymatic preparation process of chub mackerel immune active peptide. The amino acid composition of the obtained immune active peptide of chub mackerel was analyzed. The results showed that neutral protease was the best protease, and the best enzymatic hydrolysis conditions were enzyme addition 8800 U/g, time 7 h and temperature 52 ℃. The verification experiment found that the relative proliferation rate of mouse spleen lymphocytes obtained under these conditions was 48.11%±2.67%, which was close to the predicted value of regression equation. At the same time, chub mackerel immune active peptide was rich in amino acids, including 45.52% essential amino acids and 32.00% hydrophobic amino acids. The results would provide a theoretical basis for enzymatic preparation of immune active peptide for chub mackerel, and a reference for further realization of high value utilization of chub mackerel resources.

     

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