Method for preparing n-3PUFA ocean glycerin ester by enzymatical process
An enzymatic preparation and glyceride technology, applied in the fields of biotechnology and functional health care, can solve problems such as being in the blank, and achieve the effects of improving utilization rate, preventing oxidation, and easily controlling the reaction process
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example 1
[0020] Add n-hexane 7mL, glycerol 5g, n-3 PUFA concentrate 1g (from tuna fish oil, DHA and EPA content are 72% and 17%, respectively), 0.6% (w / w) water, 40mg lipase in the reaction vessel Novozym435, sealed under nitrogen protection, carried out esterification reaction at 150 times / min in a constant temperature water-bath shaker at 40°C, and after the reaction was carried out for 1 hour, 1 g of molecular sieve was added to remove the moisture generated by the reaction. After the reaction is finished, filter the reaction mixture synthesized by lipase catalysis through an anhydrous sodium sulfate bed to remove enzyme molecules and molecular sieves, and titrate the filtrate with 0.025mol / L sodium hydroxide solution (phenolphthalein as indicator) until the solution is reddish , Transfer the reaction solution to a separatory funnel, add 25 mL of n-hexane, mix well, discard the lower aqueous solution, collect the upper n-hexane layer (containing acylglycerol), and dehydrate with anhy...
example 2
[0022] Add n-hexane 5mL, glycerin 3g, n-3 PUFA concentrate 0.5g (from skipjack fish oil, DHA and EPA content are 68% and 15% respectively), 0.5% (w / w) water, 20mg in the reaction vessel Lipase Novozym435, sealed under nitrogen protection, carried out esterification reaction at 150 times / min in a constant temperature water-bath shaker at 40°C. After the reaction was carried out for 1 hour, 1 g of molecular sieve was added to remove the water generated by the reaction. After the reaction is finished, filter the reaction mixture synthesized by lipase catalysis through an anhydrous sodium sulfate bed to remove enzyme molecules and molecular sieves, and titrate the filtrate with 0.025mol / L sodium hydroxide solution (phenolphthalein as indicator) until the solution is reddish , Transfer the reaction solution to a separatory funnel, add 25 mL of n-hexane, mix well, discard the lower aqueous solution, collect the upper n-hexane layer (containing acylglycerol), and dehydrate with anhydr...
example 3
[0024] Add 10 mL of n-hexane, 7 g of glycerol, 1 g of n-3 PUFA concentrate (from snake mullet fish oil, with DHA and EPA content of 48% and 20%, respectively), 0.8% (w / w) water, and 80 mg of fat in the reaction vessel The enzyme Novozym435 was sealed under nitrogen protection, and the esterification reaction was carried out in a constant temperature water bath shaker at 40°C at 150 times / min. After the reaction was carried out for 1 hour, 1 g of molecular sieve was added to remove the water generated by the reaction. After the reaction is finished, filter the reaction mixture synthesized by lipase catalysis through an anhydrous sodium sulfate bed to remove enzyme molecules and molecular sieves, and titrate the filtrate with 0.025mol / L sodium hydroxide solution (phenolphthalein as indicator) until the solution is reddish , Transfer the reaction solution to a separatory funnel, add 25 mL of n-hexane, mix well, discard the lower aqueous solution, collect the upper n-hexane layer (...
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