HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250430Generated: October 29, 2026
Pyridoxal 5'-phosphate → L-5-Fluorotryptophan
https://huagongshe.com/reaction/1250430
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridoxal 5'-phosphate | HCID 1051 | — |
| Reactant | L-Serine | HCID 5951 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 5-Fluoroindole | HCID 67861 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | L-5-Fluorotryptophan | HCID 688357 | — |
Reaction Steps
In the same manner as in Example 1, the cell suspension of Proteus vulgaris ATCC 13315 was prepared. Subsequently, 50 ml of a solution containing 120 mg/ml L-serine, 8 mg/ml sodium sulfite and 0.2 mg/ml pyridoxal 5′-phosphate were adjusted to pH 8.8, using potassium hydroxide solution, to adjust the final volume to 80 ml (substrate solution B). Subsequently, 1 ml of cell suspension was added to the 8 ml of substrate solution B, to which was added 1 ml of a solution containing 200 mg/ml 5-fluoroindole dissolved in methanol, and was incubated at 37° C. After the reaction had proceeded for the times indicated in Table 2, the reaction was stopped with boiling for 5 minutes. The amount of 5-fluoro-L-tryptophan produced in the reaction solution for 2, 6, 18 and 30 hours of reaction is shown in Table 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06338957B2 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-6227af56086d4cdc8255bbf52137f942 |
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| Source note | uspto-grants-2002_01 |
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