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O=C[C@@H:3]([C@H:5]([C@@H:7]([C@@H:9]([CH2:11][OH:12])O)O)O)[OH:4].S([O-])([O-])(=O)=[O:14].[NH4+:18].[NH4+:19].[K].S([O-])([O-])(=O)=O.[Mg+2].CC1[N+](CC2C=NC(C)=NC=2N)=CSC=1CCO.Cl.[Cl-].OC(CCCC[C@H]1[C@@H]2[C@@H](NC(N2)=O)CS1)=O>>[NH2:18][C@H:5]([C:3]([OH:4])=[O:14])[CH2:7][CH2:9][C:11](=[O:12])[NH2:19]참가 물질
실험 절차
An aqueous solution medium having a composition of 10% of glucose, 1% of ammonium sulfate, 0.25% of potassium primary phosphate (KH2P04), 0.04% of magnesium sulfate, 0.001% of ferrous sulfate, 350 μg/l of thiamine hydrochloride, 5 μg/l of biotin and 0.5 ml/dl of Aji-Eki® which is a soybean protein hydrolysate which accelerates the growth of L-amino acid-producing microorganisms and shortens the required culture time, at pH 7.0, was charged in an amount of 300 ml into separate small sized glass jar fermenters. After sterilizing in a conventional manner, the various L-glutamine-producing bacterial strains shown in Table 10, which had been previously grown in bouillon slants at 30° C. for 24 hours, were inoculated thereon. Then, incubation was carried out at 31.5° C. for 30 hours at 1200 rpm at an aeration rate of 1/4 volume per minute, while keeping the pH at 6.5 by the addition of ammonia gas. After completion of the fermentation, the yield of L-glutamine produced and accumulated in the solution based on glucose was determined and is shown in Table 10.
후처리
- customproducing microorganisms
- additionat pH 7.0, was charged in an amount of 300 ml
- custominto separate small sized glass jar fermenters
출처 및 근거
- ORD 기록
- ord-91368b1344e648e48747bb22b5a1c04e
- 출처 데이터셋
- uspto-grants-1994_03
- 특허 번호
- US05294547
연결된 노트
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