Method for preparing egg essence by using maillard reaction
A Maillard reaction, egg technology, applied in food preparation, application, acid-containing food ingredients, etc., can solve the problems of rarity and insufficient fullness of flavor, and achieve good high temperature resistance, high safety, broad market prospects and economic effect
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Embodiment 1
[0023] Embodiment 1, a kind of method utilizing Maillard reaction to prepare egg essence, carries out following steps successively:
[0024] 1) After shelling the eggs, beat them into a slurry, weigh 100g of the slurry, add 900g of water, mix well, and obtain the egg liquid;
[0025] First use a sodium hydroxide solution with a concentration of 1.0N to adjust the pH of the egg liquid to 8.0, then heat it in a water bath at 80°C for 10 minutes; then cool it to room temperature (cooling can be achieved by running water), and then add 0.5g of Novozymes food-grade alkali Protease Alcalase 2.4L, stirred evenly, enzymatically hydrolyzed in 55°C constant temperature water bath at 200rpm for 2.0h,
[0026] After hydrolysis, raise the temperature to 90°C and keep it for 15 minutes, the purpose is to inactivate the protease; then after reaching room temperature (cooling with running water can be used), filter (pass through a 1.2μm filter membrane), and the obtained filtrate is concentra...
Embodiment 2
[0029] Embodiment 2, a kind of method utilizing Maillard reaction to prepare egg essence, carries out following steps successively:
[0030] 1) After shelling the eggs, beat them into a slurry, weigh 200g, add 800g of water, mix well, and obtain egg liquid;
[0031] First use 1.0N sodium hydroxide solution to adjust the pH of the egg liquid to 8.0, place it in a water bath at 80°C and heat it for 10 minutes, take it out and cool it to room temperature; then add 0.8g Novozymes food-grade alkaline protease Alcalase 2.4L, After stirring evenly, enzymatically hydrolyze for 3.0 hours in a constant temperature water bath at 55°C and stir at 200rpm;
[0032] After the hydrolysis, the solution was warmed up to 90°C and kept for 15 minutes in order to inactivate the protease, then cooled to room temperature, filtered (passed through a 1.2 μm filter membrane), and the obtained filtrate was concentrated to one third of its volume by rotary evaporation at 60°C in vacuum , stop concentrat...
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