Enzymatic-process preparation method for maltotriose glycosyl-beta-cyclodextrin
A maltotriosyl and maltotriose technology, applied in the field of cyclodextrin, can solve the problems of restricted application, poor water solubility of β-cyclodextrin, poor hemolytic non-digestive tract safety, etc., and achieves high production safety and saves refining Mild and controllable effects of process and cost, reaction conditions
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Embodiment 1
[0010] In the reaction system, select 3% pullulan solution, adjust the pH value to about 5.0, add pullulanase to 100U / g pullulan, control the reaction temperature at 45°C in a super constant temperature water bath, hydrolyze for 8 hours, and inactivate the enzyme in a boiling water bath , centrifuged to remove the enzyme protein, then concentrated to a certain volume by rotary evaporation to obtain high-purity maltotriose syrup, and the maltotriose content was 85% as determined by high performance liquid chromatography. Add β-cyclodextrin, adjust the mass concentration ratio of maltotriose and β-cyclodextrin to 5:1, adjust the pH value of the mixed solution to about 5.0, add pullulanase to 200U / g β-cyclodextrin, and then The reaction was incubated at 50°C for 48h. Inactivate the enzyme in a boiling water bath for 15 minutes, centrifuge to remove the enzyme protein, and then filter with a 1000Da filter membrane to remove small molecule sugars such as glucose, maltose, maltotrio...
Embodiment 2
[0012] In the reaction system, select 5% pullulan solution, adjust the pH value to about 5.0, add pullulanase to 100U / g pullulan, control the reaction temperature at 45°C in a super constant temperature water bath, hydrolyze for 8 hours, and inactivate the enzyme in a boiling water bath , centrifuged to remove the enzyme protein, then concentrated to a certain volume by rotary evaporation to obtain high-purity maltotriose syrup, and the maltotriose content was 83% as determined by high performance liquid chromatography. Add β-cyclodextrin, adjust the mass concentration ratio of maltotriose and β-cyclodextrin to 6:1, adjust the pH value of the mixture to about 5.0, add pullulanase to 200U / g β-cyclodextrin, and then The reaction was incubated at 50°C for 48h. Inactivate the enzyme in a boiling water bath for 15 minutes, centrifuge to remove the enzyme protein, and then filter with a 1000Da filter membrane to remove small molecule sugars such as glucose, maltose, maltotriose, etc...
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