毛里提油的水酶法提取:产率和抗氧化化合物

Jezica P.P. Silva, A. M. Rodrigues, L. H. M. Silva
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引用次数: 3

摘要

酶辅助水萃取是一种新兴的绿色技术,已应用于不同的油籽。本研究采用中心复合可旋转设计(CCRD)与响应面法相结合的方法,研究酶促水提法提取布里提油的工艺,以获得更高的得率和抗氧化化合物。这项研究分两步进行。首先评估了不同酶(纤维素酶、果胶酶和蛋白酶)的效率,以及在提取过程中影响较大的变量,对每种酶进行了CCRD设计。第二步选择对提取率表现最佳的酶进行,改变第一步中具有较大意义的变量的实验波段,以拓宽研究范围。在这一步骤中还评估了总类胡萝卜素、总酚类化合物和提取油的抗氧化能力。在第一个实验中,纤维素酶的产率最高,而温度和时间是最显著的变量。对于第二个设计,用纤维素酶进行,定义为最佳操作条件为55°C温度,2%酶浓度,6小时提取。在此条件下,产率为76.5%,总类胡萝卜素浓度为3,119.5µg β-胡萝卜素e.g-1。方差分析显示回归显著,拟合缺失无显著性(p<0.05)。产量和类胡萝卜素含量的测定系数分别为95.6%和94.5%。本研究中buriti油中总酚类化合物的最高测定值为254±5µg GAE。抗氧化能力为218.0±0.3µmol Trolox。g1的石油。酶法水提工艺对布里提油和含高浓度抗氧化化合物的油是可行的。
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Aqueous Enzymatic Extraction of Buriti (Mauritia Flexuosa) Oil: Yield and Antioxidant Compounds
Enzyme-assisted aqueous extraction is considered an emerging green technique that has been applied to different oilseeds. This study aimed to study the enzymatic aqueous extraction process of buriti oil using a central composite rotatable design (CCRD) combined with the response surface methodology aiming to obtain higher yield and antioxidant compounds in the oil. The study was carried out in two steps. The first assessed the efficiency of different enzymes (cellulase, pectinase, and protease) and the variables of greater influence in the extraction process, being conducted for each enzyme a CCRD design. The second step was carried out with the enzyme that showed the best performance on the extraction yield, changing the experimental bands of the variables that had greater significance in the first step, with the goal of broadening the spectrum of study. Were also evaluated in this step, total carotenoids, total phenolic compounds, and the antioxidant capacity of the oils extracted. In the first experiment, cellulase gave the highest yield, while the most significant variables were temperature and time. For the second design, performed with cellulase, were defined as optimal operating conditions at 55 °C temperature, 2% enzyme concentration and 6 hours extraction. For these conditions, the yield obtained was 76.5%, with total carotenoid concentration of 3,119.5 µg β-carotene.g-1. Analysis of variance was performed and showed the significance of the regression and non-significance of the lack-of-fit (p<0.05). The coefficients of determination of the yield and carotenoid content were 95.6% and 94.5%, respectively. The highest value of total phenolic compounds determined for buriti oil in this study was 254 ± 5 µg GAE.g-1 oil, while for the antioxidant capacity was 218.0 ± 0.3 µmol Trolox.g-1 oil. The enzymatic aqueous extraction process is viable for buriti oil and produced oils with high concentrations of antioxidant compounds.
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