A strain of Issakia orientalis and its whole cell transformation method for producing citicoline
A technology of whole-cell transformation and ESZ yeast, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve the problems of low conversion rate and yield, achieve high-efficiency preparation, and improve the effect of regeneration rate
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Embodiment 1
[0022] For the cultivation of Issa orientalis, the yeast medium used is: glucose 50 g / L, urea 2.0 g / L, potassium dihydrogen phosphate 1.5 g / L, magnesium sulfate heptahydrate 0.5 g / L, zinc sulfate heptahydrate 4.0 mg / L, ferric sulfate heptahydrate 3.0 mg / L, manganese sulfate tetrahydrate 0.3 mg / L, anhydrous calcium chloride 1.0 mg / L, biotin 0.05 mg / L, distilled water to volume. The inoculum amount of Issaccharomyces orientalis was 10%, cultured on a shaker at 30oC for 24 hours, then centrifuged at 4500r / min for 10min, and the supernatant was discarded to obtain yeast sludge, which could be used to prepare citicoline.
[0023] In the reactor, prepare 2000 g of yeast sludge and water obtained from 25 μmol / mL phosphorylcholine, 10 μmol / mL 5'-cytidylic acid, 200 μmol / mL glucose, 5 μmol / mL magnesium sulfate heptahydrate and centrifugation of the above-mentioned culture medium and water. The reaction solution was 10L, adjusted to pH 6.0 with sodium hydroxide, and converted at 32oC f...
Embodiment 2
[0025] In the reactor, prepare 25 μmol / mL phosphorylcholine, 10 μmol / mL 5'-cytidylic acid, 200 μmol / mL glucose, 5 μmol / mL magnesium sulfate heptahydrate and the method for cultivating Issahia orientalis as described in Example 1 Cultivate 10L of reaction solution consisting of 2000g of yeast sludge obtained by centrifugation and water, adjust the pH to 6.0 with sodium hydroxide, add 0.1mL / L of toluene, and transform at 32oC for 10h. After the reaction, measure the content of citicoline in the reaction solution. The yield was 2.4g / L, and the conversion rate reached 74.2%.
Embodiment 3
[0027] In the reactor, prepare 30 μmol / mL phosphorylcholine, 20 μmol / mL 5'-cytidylic acid, 300 μmol / mL glucose, 5 μmol / mL magnesium sulfate heptahydrate, 10 μmol / mL potassium dihydrogen phosphate and according to Example 1. The method of cultivating Issa orientalis is to cultivate 10L of reaction solution consisting of 5000g of yeast sludge obtained by centrifugation and water, adjust the pH to 5.0 with sodium hydroxide, add 0.5mL / L of toluene, and transform at 32oC for 10h. After the reaction, measure the reaction The output of citicoline in the solution was 5.1g / L, and the conversion rate reached 78.9%.
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