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Production and stability of structured lipids from algal oils and capric acid

机译:来自藻类油和癸酸结构脂质的生产和稳定性

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This study aimed to incorporate capric acid (CA) into selected algal oils, namely arachidoinc acid single cell oil (ARASCO), docosahexaenoic acid single cell oil (DHASCO) and the OMEGA-GOLD oil rich in dcosahexaenoic acid (DHA) and dosapentaenoic acid(n-6 DPA). Response surface methodology indicated that under optimum conditions (12.3% enzyme, 45°C, and 29.4 h) CA incorporation was 20.0% into ARASCO; (4.2% enzyme, 43.3°C, and 27.1 h) 22.6% into DHASCO and (2.5% enzyme, 46.6°C and 25.2 h) 20.7% into the OMEGA-GOLD oil. Stereospecific analysis indicated that in all oils examined CA was mainly located at the sn-1 and sn-3 positions of the resultant TAG molecules while the highly unsaturated fatty acids being primarily esterified to the sn-2 positions of the three oils. In all cases, enzymatically modified oils were more susceptible to oxidation than their unmodified counterparts.
机译:本研究旨在将癸酸(CA)掺入选定的藻类,即花生锌酸单细胞油(ARASCO),二十二碳六烯酸单细胞油(DHASCO)和富含DCOSAHENENOIN酸(DHA)和白昔烯酸的ω-金油( N-6 DPA)。响应表面方法表明,在最佳条件下(12.3%酶,45℃和29.4小时),加入Arasco的20.0%; (4.2%酶,43.3°C,27.1小时)22.6%进入DHASCO和(2.5%酶,46.6℃和25.2小时)20.7%进入ω-金油。立体特异性分析表明,在所有油中,所检查的Ca主要位于所得标签分子的Sn-1和Sn-3位置,而高度不饱和脂肪酸主要是酯化到三种油的Sn-2位置。在所有情况下,酶压改性的油比其未修饰的对应物更容易氧化。

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