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首页> 外文期刊>Brazilian Journal of Microbiology >Synthesis of structured triacylglycerols enriched in n-3 fatty acids by immobilized microbial lipase
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Synthesis of structured triacylglycerols enriched in n-3 fatty acids by immobilized microbial lipase

机译:固定化微生物脂肪酶合成富含n-3个脂肪酸的结构化三酰甘油

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The search for new biocatalysts has aroused great interest due to the variety of micro-organisms and their role as enzyme producers. Native lipases from Aspergillus niger and Rhizopus javanicus were used to enrich the n-3 long-chain polyunsaturated fatty acids content in the triacylglycerols of soybean oil by acidolysis with free fatty acids from sardine oil in solvent-free media. For the immobilization process, the best lipase/support ratios were 1:3 (w/w) for Aspergillus niger lipase and 1:5 (w/w) for Rhizopus javanicus lipase using Amberlite MB-1. Both lipases maintained constant activity for 6 months at 4 ?°C. Reaction time, sardine-free fatty acids:soybean oil mole ratio and initial water content of the lipase were investigated to determine their effects on n-3 long-chain polyunsaturated fatty acids incorporation into soybean oil. Structured triacylglycerols with 11.7 and 7.2% of eicosapentaenoic acid + docosahexaenoic acid were obtained using Aspergillus niger lipase and Rhizopus javanicus lipase, decreasing the n-6 / n-3 fatty acids ratio of soybean oil (11:1 to 3.5:1 and 4.7:1, respectively). The best reaction conditions were: initial water content of lipase of 0.86% (w/w), sardine-free faty acids:soybean oil mole ratio of 3:1 and reaction time of 36 h, at 40 ?°C. The significant factors for the acidolysis reaction were the sardine-free fatty acids:soybean oil mole ratio and reaction time. The characterization of structured triacylglycerols was obtained using easy ambient sonic-spray ionization mass spectrometry. The enzymatic reaction led to the formation of many structured triacylglycerols containing eicosapentaenoic acid, docosahexaenoic acid or both polyunsaturated fatty acids.
机译:由于微生物的多样性及其作为酶生产者的作用,寻求新的生物催化剂引起了极大的兴趣。在无溶剂介质中,用沙丁鱼油中的游离脂肪酸进行酸解,使用黑曲霉和爪哇根霉的天然脂肪酶富集大豆油三酰基甘油中n-3长链多不饱和脂肪酸的含量。对于固定过程,使用Amberlite MB-1的黑曲霉脂肪酶的最佳脂肪酶/支持比为1:3(w / w),爪哇根霉脂肪酶的最佳脂肪酶/支持比为1:5(w / w)。两种脂肪酶均在4°C下保持6个月的恒定活性。研究了反应时间,不含沙丁鱼的脂肪酸:大豆油的摩尔比和脂肪酶的初始含水量,以确定它们对掺入大豆油中的n-3长链多不饱和脂肪酸的影响。使用黑曲霉脂肪酶和爪哇根霉脂肪酶获得具有11.7和7.2%二十碳五烯酸+二十二碳六烯酸的结构化三酰甘油,从而降低了豆油的n-6 / n-3脂肪酸比例(从11:1降至3.5:1和4.7: 1)。最佳的反应条件是:脂肪酶的初始含水量为0.86%(w / w),不含沙丁鱼的脂肪酸:大豆油的摩尔比为3:1,在40°C下反应时间为36 h。酸解反应的重要因素是无沙丁鱼脂肪酸:大豆油的摩尔比和反应时间。结构化的三酰基甘油的表征是使用简单的环境声波喷雾电离质谱法获得的。酶促反应导致形成许多含有二十碳五烯酸,二十二碳六烯酸或两种多不饱和脂肪酸的结构化三酰基甘油。

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