Method for removing metaglyceride from grease
A technology of partial glyceride and monoglyceride, applied in the field of removal of partial glyceride in oil, can solve the problems of increased burden, MAG not removed, MAG difficult to effectively remove, etc., to achieve complete removal effect
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Embodiment 1
[0023] Take 200g of the oil composition, wherein the content of TAG is 102.8g, the content of DAG is 62.0g, and the content of MAG is 35.6g; add 36g of buffer solution (0.25M citric acid-NaOH) with a pH of 6.5, add 0.4g Partial glyceride lipase Lipase SMG1 (Wang W-f, Li T, Qin X-l, Ning Z-x, Yang B, Wang Y-h. Production of lipase SMG1 and its application in synthesizing diacylglyecrol[J]. Journal of Molecular Catalysis B: Enzymatic 2012; 77:87-91), while adding 0.4 g of monoglyceride lipase bMGL, and shearing the mixture for 1 min. The reaction mixture was stirred normally at 30-35°C for 30 minutes. The enzyme-treated oil is then centrifuged and the separated oily phase is collected. In the oil obtained by using partial glyceride lipase and monoglyceride lipase at the same time, the content of TAG was 50.2%, the content of DAG was 0.6%, and the content of MAG was 0.3%.
Embodiment 2
[0025] Take 200g of the oil composition, wherein the content of TAG is 102.8g, the content of DAG is 62.0g, and the content of MAG is 35.6g; add 36g of buffer solution (0.25M citric acid-NaOH) with a pH of 6.5, add 0.4g The partial glyceride lipase Lipase SMG1 was added simultaneously with 0.4 g of the monoglyceride lipase bMGL, and the mixture was sheared for 1 min. The reaction mixture was stirred normally at 30-35°C for 1 hour. The enzyme-treated oil is then centrifuged and the separated oily phase is collected. In the oil obtained by using partial glyceride lipase and monoglyceride lipase at the same time, the content of TAG was 50.2%, the content of DAG was 0.4%, and the content of MAG was 0.3%.
Embodiment 3
[0027] Take 200g of the oil composition, wherein the content of TAG is 102.8g, the content of DAG is 62.0g, and the content of MAG is 35.6g; add 72g of buffer solution (0.25M citric acid-NaOH) with a pH of 6.5, add 0.4g The partial glyceride lipase Lipase SMG1 was added simultaneously with 0.4 g of the monoglyceride lipase bMGL, and the mixture was sheared for 1 min. The reaction mixture was stirred normally at 30-35°C for 30 minutes. The enzyme-treated oil is then centrifuged and the separated oily phase is collected. In the oil obtained by using partial glyceride lipase and monoglyceride lipase at the same time, the content of TAG was 51.1%, the content of DAG was 0.3%, and the content of MAG was 0.25%.
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