HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571583Generated: October 30, 2026
Pyridoxal 5'-phosphate → 7-Methoxy-2-tetralone
https://huagongshe.com/reaction/571583
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridoxal 5'-phosphate | HCID 1051 | — |
| Reactant | Ampicillin | HCID 6249 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | (S)-7-methoxy-2-aminotetraline | HCID 11008478 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 7-Methoxy-2-tetralone | HCID 77785 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029113B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-8f3a57902add4c02a3519cbb261a05ab |
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| Source note | uspto-grants-2015_05 |
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