操作条件对红罗非鱼鱼鳞化学水解产物抗氧化和铁螯合活性的影响

L. Sierra, J. E. Zapata
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引用次数: 1

摘要

本研究的目的是优化碱性水解提取具有抗氧化和铁螯合活性的RTS蛋白的工艺。红罗非鱼(Oreochromis sp.)鳞片(RTS)含有必需蛋白质;因此,这些代表了获得水解物的机会,这些水解物可能具有感兴趣的生物活性。对于蛋白质的提取,可以使用化学方法,如碱性水解。中心复合设计(DOE)的影响因素为NaOH浓度(0.5 ~ 2M)、温度(40 ~ 60℃)和水垢百分比(2.5 ~ 7.5%)。响应变量为:蛋白质(g/L)、抗氧化能力(ABTS和FRAP)和铁螯合活性百分比(ICH)。在500ml反应器中持续搅拌2、4和8 h,评估水解时间。对于所评估的变量,有可能获得显著的模型,这些模型表明,在较高的温度、NaOH浓度和底物浓度下,可获得较高浓度的可溶性蛋白质,而不会影响所评估的生物活性。在最佳DOE条件下,获得的蛋白质量为20 g/L,提取率为98%。获得具有生物活性蛋白的最佳时间为2 h。本研究证明了采用碱性水解法可获得具有抗氧化和铁螯合活性的RTS蛋白水解产物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Operation Conditions on Antioxidant and Iron Chelating Activity of Chemical Hydrolysates from Red Tilapia (Oreochromis sp.) Scales
The aim of this study was to optimize the alkaline hydrolysis to extract protein from RTS with antioxidant and iron chelating activity. Red Tilapia (Oreochromis sp.) scales (RTS) have essential protein contents; therefore, those represent an opportunity to obtain hydrolysates, which may present biological activities of interest. For the extraction of the protein, it is possible to use chemical methods such as alkaline hydrolysis. The factors of central composite design (DOE) were NaOH concentration (0.5 to 2M), temperature (40 to 60°C) and percentage of scales (2.5 to 7.5%). The response variables were: protein (g/L), antioxidant capacity (ABTS and FRAP) and percentage of iron chelating activity (ICH). The hydrolysis time was evaluated in 2, 4 and 8 h in a 500 mL reactor with constant stirring. It was possible to obtain significant models for the variables assessed and those showed that with high levels of temperature, NaOH concentration and substrate concentration get a higher concentration of soluble protein without affecting the biological activities evaluated. The quantity of the protein obtained for the optimal DOE conditions was 20 g/L, with an extraction yield of 98%. The best time to get proteins with bioactivity was 2 h. This study evidenced the obtainment of protein hydrolysates from RTS with antioxidant and iron chelating activity using alkaline hydrolysis.
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