Method for degumming with magnetic immobilized phospholipase A2
An enzyme immobilized and magnetic technology, applied in the direction of edible oil/fat, application, and fat production, can solve the problems of difficult repeated or continuous use, difficult separation and recovery, and difficult removal of non-hydratable phospholipids.
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specific Embodiment approach 1
[0006] Specific embodiment 1: A magnetically immobilized PLA 2 The method of degumming is achieved through the following steps: 1. PLA 2 Immobilization: First, 1.0g of magnetic microspheres PVP-DB-171 (polyvinylpyrrolidone-vinyltrimethoxysilane) / SiO 2 / Fe 3 O 4 Soaked in 50mL phosphate buffer (0.1M, pH=7.0) for 24 hours, then magnetically separated, and then add the soaked carrier to a certain amount of phosphate buffer containing 0.2% phospholipase (0.1M , PH=7.0), while slowly stirring the reaction with a magnetic stirrer at 45°C for a period of time, and finally magnetic separation and washing the immobilized enzyme with phosphate buffer (0.1M, pH=7.0). The filtrate and washing liquid are combined to determine the content of enzyme protein, and the immobilized enzyme obtained is stored in a refrigerator at 4°C; 2. Magnetically immobilized PLA 2 For degumming: Take 200 g of soybean oil, preheat it to 55°C, mix the immobilized phospholipase with a certain amount of deionized wat...
specific Embodiment approach 2
[0007] Specific embodiment two: this embodiment is different from specific embodiment one in that in step two, the initial pH value in the oil phase is 4.0-11.0 for immobilization of PLA 2 The other steps of degumming soybean crude oil are the same as in the first embodiment.
specific Embodiment approach 3
[0008] Specific embodiment three: This embodiment is different from specific embodiment one in that in step two, the initial pH value in the oil phase is 4.0 to 11.0, and the reaction time is 20 to 120 min. 2 Degumming of soybean oil. The other steps are the same as in the first embodiment.
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