Novel production process for extracting soy isoflavones aglycones
A technology for isoflavone aglycone and production process, which is applied in the field of novel production technology for extracting soybean isoflavone aglycone, can solve problems such as unsatisfactory soybean isoflavone aglycone, and achieves high yield, high conversion rate, and production process operation. easy effect
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Embodiment 1
[0015] Example 1: 500g of soybean powder, crushed to a particle size of 0.5mm-5.0mm, extracted twice with 3000ml of 70% ethanol under reflux, each time for 2 hours, combined extracts, concentrated in vacuum, controlled vacuum degree above -0.80MPa, The temperature is below 70°C, after concentration, the ethanol concentration is controlled to be less than 5%, and 0.5g CaCl is added to the concentrate 2 Stir the electrolyte, filter the protein after sedimentation, transfer the filtrate to a 500ml HPD100 macroporous resin column for adsorption, first wash the impurities with 1000ml pure water, then analyze with 1000ml 45% ethanol aqueous solution, concentrate the solution in vacuum, and control the vacuum at -0.80 Above MPa, temperature below 70°C, the volume of the concentrated solution is about 100ml, add 1g of solid cellulase to the concentrated solution, stir evenly, control the temperature at 45-50°C, enzymatically hydrolyze for 48 hours, add 50ml of ethyl acetate to extract,...
Embodiment 2
[0016] Example 2: 500g of soybean powder, crushed to a particle size of 0.5mm-5.0mm, extracted twice with 3000ml of 80% ethanol under reflux, each time for 3 hours, combined extracts, concentrated in vacuum, controlled vacuum degree above -0.80MPa, The temperature is below 70°C, after concentration, the ethanol concentration is controlled to be less than 5%, and 0.5g CaCl is added to the concentrate 2 Stir the electrolyte, filter the protein after sedimentation, transfer the filtrate to a 500ml D101 macroporous resin column for adsorption, first wash the impurities with 1000ml pure water, then analyze with 1000ml 70% ethanol aqueous solution, concentrate the solution in vacuum, and control the vacuum at -0.80 Above MPa, temperature below 70°C, volume of concentrated solution is about 100ml. Add 1g of solid cellulase to the concentrated solution, stir evenly, control the temperature at 45-50°C, enzymatically hydrolyze for 36 hours, add 50ml of ethyl acetate for extraction, repe...
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