Method for directionally preparing dextran
A technology of dextran and sugar solution, which is applied in the field of preparation of pharmaceutical raw materials, and can solve problems such as the application of highland barley polysaccharide extracts that have not yet appeared
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Embodiment 1
[0027] (1) Dextran sucrase extraction
[0028] Culture Leuconostoc enterococcus to the logarithmic phase, and inoculate the enzyme production medium according to the inoculum size of 0.4%. The medium is: sucrose 50g / L, yeast extract 12.5g / L, beef extract 20g / L, dihydrogen phosphate Potassium 1.0g / L, disodium hydrogen phosphate 3.6g / L, sterilized by high-pressure steam at 121°C for 15-20min; the culture conditions are 20-30°C, 100-200r / min, and the time is 20-30h. After the cultivation, the Leuconostoc enterococcus culture solution containing the crude enzyme solution was obtained. The crude enzyme solution is obtained by centrifugation in a centrifuge at a speed of 8000-10000r / min for 15-20 minutes. After centrifugation, the precipitate is discarded, and the supernatant is collected as the crude enzyme solution.
[0029] (2) Enzymolysis of barley extract
[0030] Use pure water to prepare 100 mL of highland barley extract mixture with a mass concentration of 10%, add 5% amyl...
Embodiment 2
[0038] (1) Dextran sucrase extraction
[0039] Culture Leuconostoc enterococcus to the logarithmic phase, and inoculate the enzyme production medium according to the inoculum size of 0.4%. The medium is: sucrose 50g / L, yeast extract 12.5g / L, beef extract 20g / L, dihydrogen phosphate Potassium 1.0g / L, disodium hydrogen phosphate 3.6g / L, sterilized by high-pressure steam at 121°C for 15-20min; the culture conditions are 20-30°C, 100-200r / min, and the time is 20-30h. After the cultivation, the Leuconostoc enterococcus culture solution containing the crude enzyme solution was obtained. The crude enzyme solution is obtained by centrifugation in a centrifuge at a speed of 8000-10000r / min for 15-20 minutes. After centrifugation, the precipitate is discarded, and the supernatant is collected as the crude enzyme solution.
[0040] Add 0.005% CaCl to the crude enzyme solution during storage 2 , stored at 4 ℃, can prolong its storage time.
[0041] (2) Enzymolysis of barley extract
...
Embodiment 3
[0050] (1) Dextran sucrase extraction
[0051] Culture Leuconostoc enterococcus to the logarithmic phase, and inoculate the enzyme production medium according to the inoculum size of 0.4%. The medium is: sucrose 50g / L, yeast extract 12.5g / L, beef extract 20g / L, dihydrogen phosphate Potassium 1.0g / L, disodium hydrogen phosphate 3.6g / L, sterilized by high-pressure steam at 121°C for 15-20min; the culture conditions are 20-30°C, 100-200r / min, and the time is 20-30h. After the cultivation, the Leuconostoc enterococcus culture solution containing the crude enzyme solution was obtained. The crude enzyme solution is obtained by centrifugation in a centrifuge at a speed of 8000-10000r / min for 15-20 minutes. After centrifugation, the precipitate is discarded, and the supernatant is collected as the crude enzyme solution. Add 0.005% CaCl to the crude enzyme solution during storage 2 , stored at 4 ℃, can prolong its storage time.
[0052] (2) Enzymolysis of barley extract
[0053] Us...
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