酶水解作为牛肺的增值策略:过程变量的优化和抗氧化能力的研究

JSFA reports Pub Date : 2023-03-21 DOI:10.1002/jsf2.110
F. G. Martinez, V. A. Ambrosi, G. Rocha, A. M. Sancho, N. Szerman
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引用次数: 0

摘要

肉类产量的增加也意味着副产品或可食用内脏的增加。由于蛋白质含量高,这些副产物可以作为底物来获得具有功能活性的水解产物。本研究旨在通过生产具有抗氧化能力的水解物来激活牛肺。结果采用中心复合设计,采用响应面法研究温度(43.2 ~ 76.8℃)、酶/底物比(ES: 0.65 ~ 4.85% (w/w)) (Alcalase∶2.4 L/Flavourzyme∶1:1)和pH(5.8 ~ 9.2)。通过ABTS、DPPH和FRAP方法评价所得BLH(牛肺水解物)的抗氧化能力。在53岁时达到最大抗氧化能力。°C, ES比2.3% (w/w), pH为8.2。在最佳水解条件下,从反应开始到反应30 min,抗氧化能力迅速增加,在反应120 min时达到最大值;然后逐渐减小,直至结束(180 min)。水解的程度随着水解的发生而增加,最高可达45%。通过Tricine-SDS-PAGE和SEC-FPLC对BLH的分子量分布进行了分析,结果表明,水解120 min的牛肺蛋白中存在低分子量肽(< 5kda),而非水解样品中不存在。结论本研究优化了利用商业蛋白酶在短时间内生产具有抗氧化能力的BLH的工艺参数,为肉类工业副产品的回收提供了一个有价值的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enzymatic hydrolysis as a valorization strategy of bovine lungs: Optimization of process variables and study of antioxidant capacity

Background

The increase in meat production would also imply an increase in the generation of by-products or edible offal. These by-products can be used, due to their high protein content, as a substrate to obtain hydrolysates with functional activities. This study aimed to valorize bovine lungs by producing hydrolysates with antioxidant capacity.

Results

A response surface methodology study was carried out using a central composite design in which factors were temperature (43.2–76.8°C), enzyme/substrate ratio [ES: 0.65–4.85% (w/w)] using Alcalase 2.4 L/Flavourzyme (1:1) and pH (5.8–9.2). The antioxidant capacity of the obtained BLH (bovine lung hydrolysates) was evaluated by the ABTS, DPPH, and FRAP methods. The maximum antioxidant capacity was achieved at 53.°C, ES ratio of 2.3% (w/w), and pH of 8.2. Under optimal hydrolysis conditions, the antioxidant capacity increased rapidly from the beginning of the reaction to 30 min, reaching a maximum at 120 min; then, it decreased until the end (180 min). The degree of hydrolysis increased as hydrolysis occurred up to a maximum of 45%. Molecular weight distribution of BLH evaluated by Tricine-SDS-PAGE and SEC-FPLC showed that bovine lung proteins hydrolyzed for 120 min presented low molecular weight peptides (<5 kDa), which are absent in the non-hydrolyzed sample.

Conclusion

In this work, we optimized the variables for producing BLH with antioxidant capacity using commercial proteases in a short reaction time, making it a worthwhile strategy for the recovery of by-products from the meat industry.

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