تفاعل #658765

ord-8f3a57902add4c02a3519cbb261a05ab

معادلة التفاعل

Cc1ncc(COP(=O)(O)O)c(C=O)c1O
pyridoxal phosphate
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O
ampicillin
COc1ccc2c(c1)C[C@@H](N)CC2
(S)-7-methoxy-2-aminotetralin
O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium phosphate
COc1ccc2c(c1)CC(=O)CC2
7-Methoxy-2-Tetralone

المذيبات

ظروف التفاعل

درجة الحرارة
30°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىcoli obtained in Example 2
  2. 2
    أخرىthe mixture was sonicated so that
  3. 3
    استخلاصa cell-free extract
  4. 4
    أخرىwas obtained
  5. 5
    استخلاصSubsequently, 100 μL of the cell-free extract
  6. 6
    workup.ADDITIONwas added to 305 μL of a substrate solution
  7. 7
    أخرىto react at 30° C. for 1 hour
  8. 8
    أخرىthe reaction

الإجراء التجريبي

The recombinant E. coli obtained in Example 2 was inoculated into 5 mL of a 2× YT medium containing 200 μg/mL of ampicillin and cultured with shaking at 30° C. for 28 hours. To 500 μL of the resulting culture liquid was added 500 μL of a 0.2 M potassium phosphate buffer (pH 7.5) containing 1 mM pyridoxal phosphate, and the mixture was sonicated so that a cell-free extract was obtained. Subsequently, 100 μL of the cell-free extract was added to 305 μL of a substrate solution having the composition shown below. After the mixture was allowed to react at 30° C. for 1 hour, 50 μL of 6 N hydrochloric acid was added to stop the reaction. The optical purity of the produced (S)-7-methoxy-2-aminotetralin was measured using HPLC under the conditions shown below. As a result, the modified enzymes shown in Table 2 had stereoselectivity higher than that of the wild-type.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09029113B2uspto-grants-2015_05