반응 #1004447
ord-b6c72e16786a44f1aa073b75264eaa95
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후처리
- 1기타the mixture formed
- 2workup.ADDITIONwas then treated in an autoclave (121° C., 98 kPa pressure, 10 minutes)
- 3workup.ADDITIONThereafter, the culture medium treated
실험 절차
220 parts by weight of this glucose was mixed with 12,100 parts by weight of a culture medium (10 g/l of peptone, 5 g/l of yeast extract, 2 g/l of meat extract, 5 g/l of NaCl, 2 g/l of cysteine hydrochloride and 5 g/l of calcium carbonate), and the mixture formed was injected into a pressure bottle. After the gaseous-phase portion in the bottle was displaced with nitrogen gas, the bottle was hermetically closed with a butyl rubber stopper, which was then treated in an autoclave (121° C., 98 kPa pressure, 10 minutes). Thereafter, the culture medium treated was cooled to 30° C., and 121 parts by weight of a pre-culture fluid of phenyllactic acid productive strain HICA432 isolated in the manner as described previously was added thereto by means of a syringe when the bottle was kept hermetically stoppered, followed by a static culture at 30° C. for 3 days. Thereafter, the culture fluid was filtered, and the water and volatile components of the filtrate obtained were evaporated off under normal-temperature reduced pressure, followed by purification to obtain 10 parts by weight of phenyllactic acid.