Method for preparing DAG by enzymolysis of TAG
A technology for triglyceride lipase and diglyceride, applied in 1 field, can solve the problems of low purity of 1,3-DAG, difficulty in large-scale production by direct esterification method, residual organic solvent, etc., so as to improve the tendency of 2-position selection properties, shortening the hydrolysis time, and increasing the added value
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Embodiment 1
[0048] 1. Mix 1000g soybean oil with 100g water, add 100g ethanol; homogenize at a high speed of 5000rpm for 20min to prepare an emulsion;
[0049] 2. Heat the emulsion to 70°C and keep it at a constant temperature, and adjust the pH of the emulsion to 7.0 with hydrochloric acid or sodium hydroxide;
[0050] 3. Add 20g of Candida antarctica lipase A;
[0051] 4. After 22 hours of reaction, the reaction ends;
[0052] 5. The reaction system was centrifuged, and the oil phase was molecularly distilled to separate monoglyceride and NEFA, diglyceride and triglyceride; the proportion of 1,3-diglyceride in the diglyceride phase was 83%.
Embodiment 2
[0054] 1. Mix 1000g of soybean oil with 100g of water, add 2.7g of ferric chloride hexahydrate and 1.98g of manganese chloride tetrahydrate; homogenize at a speed of 5000rpm for 20min at high speed to prepare an emulsion;
[0055] 2. Heat the emulsion to 70°C and keep it at a constant temperature, and adjust the pH of the emulsion to 7.0 with sodium hydroxide or hydrochloric acid;
[0056] 3. Add 20g of Candida antarctica lipase A;
[0057] 4. After 18 hours of reaction, the reaction ends;
[0058] 5. The reaction system was centrifuged, and the oil phase was molecularly distilled to separate monoglyceride and NEFA, diglyceride and triglyceride; the proportion of 1,3-diglyceride in the diglyceride phase was 78%.
Embodiment 3
[0060] 1. Mix 1000g of soybean oil with 100g of water, add 100g of ethanol, 2.7g of ferric chloride hexahydrate and 1.98g of manganese chloride tetrahydrate; homogenize at a speed of 5000rpm for 20 minutes at high speed to prepare an emulsion;
[0061] 2. Heat the emulsion to 70°C and keep it at a constant temperature, and adjust the pH of the emulsion to 7.0 with sodium hydroxide or hydrochloric acid;
[0062] 3. Add 20g of Candida antarctica lipase A;
[0063] 4. After 16 hours of reaction, the reaction ends;
[0064] 5. The reaction system was centrifuged, and the oil phase was molecularly distilled to separate monoglyceride and NEFA, diglyceride and triglyceride; the proportion of 1,3-diglyceride in the diglyceride phase was 85%.
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