Preparation method of grease with humanized structure
A technology of structured oil and breast milk, applied in dairy products, edible oil/fat, milk preparations, etc., can solve the problems of inappropriate content of palmitic acid at the Sn-2 position, complex production process, short reaction time, etc., and achieve enzyme duplication The effect of high number of times of use, wide range of applications, and short reaction time
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Embodiment 1
[0042] (1) Put 50g of palm oil with a palmitic acid content of 58.3% into a 250mL round bottom flask, place it in a water-bath shaker at 60°C, add 10g of non-specific lipase Novozym 435 (purchased from Novozymes, Denmark, enzyme Live is 10000PLU / g), reacted 5 hours with the rotating speed shaker of 250 rev / mins, filter and remove non-specific lipase, adopt gas chromatography-hydrogen flame ionization detector (GC-FID) to detect, Sn in the product -2 palmitic acid content is 58.7%.
[0043] (2) Triglyceride 50g and 125g mixed fatty acid (capric acid 3%, lauric acid 10%, myristic acid 4%, stearic acid 10%, oleic acid 50% triglyceride 50g and 125g with Sn-2 position palmitic acid content , linoleic acid 20%, linolenic acid 3%) were put into 250mL round bottom flask, placed in 60 ℃ water-bath shaker, added 17.5g 1, 3 specificity lipase Lipozyme RM IM (purchased from Denmark Novozymes company, the enzyme activity is 5-6BAUN / g), and reacted for 3 hours with a rotating speed shaker ...
Embodiment 2
[0046] (1) Put 20g of palm oil with a palmitic acid content of 58.3% into a 250mL round-bottomed flask, add 80mL of n-hexane, place it in a water bath shaker at 55°C, add 3g of non-specific lipase Novozym 435 (purchased from Denmark Nuo Weixin Company, enzyme activity is 10000PLU / g), with 250 rpm speed shaker reaction for 4 hours, filter to remove non-specific lipase, adopt gas chromatography-hydrogen flame ionization detector (GC-FID) to carry out Detection shows that the content of palmitic acid at Sn-2 position in the product is 58.1%.
[0047] (2) Triglyceride 10g and 30g mixed fatty acid (capric acid 3%, lauric acid 10%, myristic acid 4%, stearic acid 10%, oleic acid 50% triglyceride 10g and 30g mixed fatty acid with Sn-2 position palmitic acid content , linoleic acid 20%, linolenic acid 3%) are put into 250mL round bottom flask, add 160mL n-hexane, place in 55 ℃ water-bath shaker, add 6g 1,3 specificity lipase Lipozyme TL IM (purchased from Danish Novozymes company, enz...
Embodiment 3
[0050] (1) 100g of palm oil with a palmitic acid content of 58.3% is put into a 1L glass reactor, and after dehydration at 110°C for 1 hour under a vacuum of 0.08MPa, 1g of sodium ethylate is added, vacuumed at 90°C (air residual pressure lower than 0.06MPa) and stirred for 60 minutes, then cooled to 60°C, added 5mL of 10% citric acid to stop the reaction, stirred for 10 minutes and then washed with warm water at 30°C for 10 minutes to remove sodium ethoxide. Detected by gas chromatography-hydrogen flame ionization detector (GC-FID), the content of Sn-2 palmitic acid in the product is 59.1%.
[0051] (2) Triglyceride 50g and 100g mixed fatty acid (capric acid 3%, lauric acid 10%, myristic acid 4%, stearic acid 10%, oleic acid 50% triglyceride 50g with 59.1% content of Sn-2 position palmitic acid , 20% linoleic acid, 3% linolenic acid) into a 250mL round bottom flask, placed in a water bath shaker at 55°C, and added 15g of 1,3-specific lipase Lipozyme TL IM (purchased from Novo...
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