Solid phase support crosslinking enzyme aggregation and method for preparing the same
A technology of aggregates and cross-linked enzymes, applied to biochemical equipment and methods, fixed on or in inorganic carriers, fixed on/in organic carriers, etc., can solve problems such as inability to recycle and reuse, and achieve Easy optimization of reaction conditions, simple method, and the effect of high liquid flow rates
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Embodiment 1
[0027] Example 1 Preparation of immobilized cross-linked organophosphate degrading enzyme aggregates
[0028] Weigh the organophosphorus degrading enzyme and dissolve it in phosphate buffer solution to prepare an enzyme solution with a protein concentration of 0.4 mg / ml, and add porous microspheres (polystyrene type non-polar adsorption resin, model ADS-5; average pore diameter The particle size is 30nm and the particle size is greater than 100μm; performance: it does not adsorb proteins, sugars, inorganic acids, alkalis, salts, and small-molecular hydrophilic organic substances; it has high resistance to heat, acid, alkali, organic solvents, etc. Stability. Tianjin Nankai Hecheng Science and Technology Co., Ltd. formula), stirred slowly at 4°C for 3 hours; then added ammonium sulfate to a saturation of 67.5%, stirred slowly at 4°C for 5 hours; added glutaraldehyde (25%) The solution was stirred slowly at 4°C for 18 hours to a final concentration of 2.2%; the porous microspher...
Embodiment 2
[0030] Weigh lactase and dissolve it in phosphate buffered saline, prepare an enzyme solution with a protein concentration of 0.5 mg / ml, add porous microspheres (polystyrene type non-polar adsorption resin, model is ADS-5. The average pore size is 30nm , the particle size is greater than 100 μm; performance: it does not adsorb proteins, sugars, inorganic acids, alkalis, salts, and small-molecular hydrophilic organic compounds; it has high stability under conditions such as heat, acid, alkali, and organic solvents (produced by Tianjin Nankai Hecheng Technology Co., Ltd.), and stirred slowly at 4°C for 3 hours. Add ammonium sulfate to a saturation of 67.5%, and stir slowly at 4°C for 5 hours. Add glutaraldehyde (25%) solution to a final concentration of 2.2%, and stir slowly at 4°C for 18 hours. The porous microspheres were taken out by filtration, and rinsed repeatedly until the solution was clear.
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