반응식
C1N(CCO)CCN(CCS(O)(=O)=O)C1.[OH-].[Na+].CC1C(O)=C(C=O)C(COP(O)(O)=O)=CN=1.[CH2:34]1[CH2:41][C@H:40]([NH2:42])[C:38](=[O:39])[NH:37][CH2:36][CH2:35]1.OP(O)(O)=O>C1(C)C=CC=CC=1>[CH2:34]1[CH2:41][C@@H:40]([NH2:42])[C:38](=[O:39])[NH:37][CH2:36][CH2:35]1.[CH2:34]1[CH2:41][C@H:40]([NH2:42])[C:38](=[O:39])[NH:37][CH2:36][CH2:35]1참가 물질
실험 절차
Then 100 mg of these lyophilized cells from each monoculture were added to a reaction mixture consisting of 10 mM HEPES-NaOH buffer (pH 7.7), toluene (2,5 v/v %), pyridoxal-5-phosphate (20 μM), and L-α-amino-ε-caprolactam (2.5 m %). Chemical blanks (with the assay mixture without the lyophilized cells) were used as a negative control. All reaction mixtures (including the blanks) were incubated for approximately 72 hours at 40° C. before the reaction was stopped by the addition of 9 volumes of 1 M H3PO4. After removal of the cells by filtration through a 0.45 μM filter, these reaction mixtures were analyzed by the HPLC method described above to determine the concentration of D- and L-α-amino-ε-caprolactam. Finally, monocultures that formed D-α-amino-ε-caprolactam from the L-α-amino-ε-caprolactam substrate were sent to the NCIMB for strain determination. Nb. no D-α-amino-ε-caprolactam could be determined in the chemical blanks.
후처리
- additionThen 100 mg of these lyophilized cells from each monoculture were added to a reaction mixture
- customAll reaction mixtures (
- customAfter removal of the cells
- filtrationby filtration through a 0.45 μM
- filtrationfilter
- customthese reaction mixtures
출처 및 근거
- ORD 기록
- ord-2c1aa305598d45a992ce5851134dedfa
- 출처 데이터셋
- uspto-grants-2008_05
- 특허 번호
- US07371555B2
연결된 노트
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