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中国精品科技期刊2020
丛之慧,李迪,周法婷,等. 柠檬籽蛋白提取工艺优化及其不同酶解肽抗氧化活性分析[J]. 华体会体育,2022,43(16):220−229. doi: 10.13386/j.issn1002-0306.2021110117.
引用本文: 丛之慧,李迪,周法婷,等. 柠檬籽蛋白提取工艺优化及其不同酶解肽抗氧化活性分析[J]. 华体会体育,2022,43(16):220−229. doi: 10.13386/j.issn1002-0306.2021110117.
CONG Zhihui, LI Di, ZHOU Fating, et al. Optimization of Extraction Process and Antioxidant Activity of Different Enzymolysis Peptides[J]. Science and Technology of Food Industry, 2022, 43(16): 220−229. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021110117.
Citation: CONG Zhihui, LI Di, ZHOU Fating, et al. Optimization of Extraction Process and Antioxidant Activity of Different Enzymolysis Peptides[J]. Science and Technology of Food Industry, 2022, 43(16): 220−229. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021110117.

柠檬籽蛋白提取工艺优化及其不同酶解肽抗氧化活性分析

Optimization of Extraction Process and Antioxidant Activity of Different Enzymolysis Peptides

  • 摘要: 为有效利用柠檬籽资源,对其蛋白质及酶解肽的抗氧化活性进行探究,本研究采用碱提酸沉法提取柠檬籽蛋白,利用响应面法对柠檬籽蛋白提取工艺进行优化,并对其进行氨基酸组成分析。用木瓜蛋白酶、胰蛋白酶、复合蛋白酶、风味蛋白酶分别对柠檬籽蛋白进行酶解,对酶解产物的抗氧化能力(1,1-二苯基-2-三硝基苯肼自由基(DPPH·)、羟自由基(·OH)、超氧阴离子(O2·)清除能力)进行研究,并对以上四种酶解肽进行红外光谱分析。结果表明,柠檬籽蛋白最佳提取工艺条件:pH10.5,时间60 min,液料比41:1 mL/g,提取温度40 ℃,在此工艺条件下柠檬籽蛋白的得率为12.25% ± 0.01%,柠檬籽蛋白必需氨基酸种类齐全,占氨基酸总量的31.8%。风味蛋白酶酶解肽抗氧化能力较强。木瓜蛋白酶酶解肽、胰蛋白酶酶解肽、复合蛋白酶酶解肽、风味蛋白酶酶解肽清除\mathrmD\mathrmP\mathrmP\mathrmH\cdot \mathrm的IC50值分别3.54、1.75、1.52、1.02 mg/mL;清除\cdot \mathrmO\mathrmH的IC50值分别为8.77、8.92、8.29、5.02 mg/mL;清除\mathrmO_2^-\cdot的IC50值分别2.70、0.90、0.97、0.81 mg/mL。红外光谱分析表明,四种样品均在3400、1600、 1300、1000 cm−1附近有吸收峰,且含有抗氧化活性的官能团。研究认为,柠檬籽肽具有较高的抗氧化活性及营养价值,可以作为功能性成分用于抗氧化相关的功能食品和保健品的开发。

     

    Abstract: In order to utilize lemon seed resources effectively , the antioxidant activities of its protein and enzymolysis peptide were studied. Lemon seed protein(LSP) was extracted from lemon seed meal powder with the alkaline extraction and acid precipitation. Response surface methodology was used to optimize the extraction process of LSP and analyze its amino acid composition. Papain, trypsin, compound protease and flavor protease were applied on the enzymatic hydrolysis of LSP. The antioxidant capacity (scavenging capacity of 1,1- diphenyl -2- picrylhydrazyl radical (\mathrmD\mathrmP\mathrmP\mathrmH\cdot), hydroxyl radical(\cdot \mathrmO\mathrmH) and superoxide anion(\mathrmO_2^-\cdot)) of the enzymatic hydrolysate was studied, and the infrared spectrum analysis of the above four enzymatic peptides was carried out. The results showed that, the optimum extraction conditions of LSP were as follows: pH was 10.5, extraction time was 60 min, liquid-to-material ratio was 41:1 mL/g, and extraction temperature was 40 ℃. Under these conditions, the actual extraction rate of protein from lemon seed reached 12.25% ± 0.01%. The essential amino acids of LSP were complete in variety, accounting for 31.8% of the total amino acids. The flavor protease-hydrolyzed peptide had strong antioxidant capacity. The IC50 of papain enzymolysis peptide, trypsin-hydrolyzed peptide, peptide of compound protease and peptide of flavourzyme against DPPH free radical scavenging was 3.54, 1.75, 1.52 and 1.02 mg/mL, respectively. The IC50 against \cdot \mathrmO\mathrmH free radical scavenging was 8.77, 8.92, 8.29 and 5.02 mg/mL, respectively. The IC50 against \cdot \mathrmO\mathrmH free radical scavenging was 2.70, 0.90, 0.97 and 0.81 mg/mL. Theinfrared reflectance spectroscopy analysis suggested that all four samples had absorption peaks near 3400, 1600, 1300, and 1000 cm-1, and contained functional groups with antioxidant activity. The study considered that LSP had high antioxidant activity and nutritional value, and could be used as a functional component in the development of antioxidant-related functional foods and health care products.

     

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