Sulfuric Acid → HCID 54545516, compound

Temperature

30 °C

A medium comprising 2% of glucose, 1% of yeast extract, 1% of peptone, 10 ppm of MnSO4 and 1% of calcium carbonate was used for lactic acid bacteria; a medium comprising 1% of glucose, 0.5% of yeast extract, 0.5% of peptone, 0.5% of meat extract and 0.5% of NaCl (pH 7) was used for other bacteria; and a medium comprising 2% of glucose, 0.3% of yeast extract, 0.5% of peptone and 0.3% of malt extract (pH 6) was used for yeasts. 100 ml of each medium was introduced into a 500-ml Erlenmeyer flask and sterilized. Then one platinum loopful of each strain listed in Table 1 was inoculated into the corresponding medium and subjected to rotary shaking culture for 48 hours. After the completion of the culture, the cells were separated by centrifuging and washed with a physiological saline solution once to thereby yield viable cells. 50 ml of distilled water was introduced into a 500-ml Erlenmeyer flask and the above-mentioned viable cells were suspended therein. After adding 5 g of sucrose and 0.5 g of calcium carbonate thereto, the mixture was shaken at 30° C. for 10 minutes. Then 0.5 g of potassium 2-keto-4-phenyl-3-butenoate was added thereto and the mixture was allowed to react under shaking at 30° C. for 40 hours. After the completion of the reaction, the pH value of the reaction mixture was adjusted to 1 or below with sulfuric acid. It was then extracted with 100 ml of ethyl acetate, and the solvent was removed from the extract. Then the amount and optical purity of the (R)-2-hydroxy-4-phenyl-3-butenoic acid thus formed were determined by high-performance liquid chromatography.

1. extractionextract
2. extractionextract
3. extraction0.5% of peptone, 0.5% of meat extract
4. extractionextract
5. extraction0.5% of peptone and 0.3% of malt extract (pH 6)
6. addition100 ml of each medium was introduced into a 500-ml Erlenmeyer flask
7. customAfter the completion of the culture, the cells were separated by centrifuging
8. washwashed with a physiological saline solution once
9. customto thereby yield viable cells
10. customto react
11. stirringunder shaking at 30° C. for 40 hours
12. customAfter the completion of the reaction
13. extractionIt was then extracted with 100 ml of ethyl acetate
14. customthe solvent was removed from the extract

ORD record

ord-f1570251abf14e08a3768932fba4551a

Source dataset

uspto-grants-1993_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05194380