Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridoxal 5'-phosphate | HCID 1051 | — |
| Reactant | 3-Phenylpyruvate | HCID 4592697 | — |
| Reactant | Ammonium Aspartate | HCID 86590683 | — |
| Solvent | Water | HCID 962 | — |
| Product | L-Phenylalanine | HCID 6140 | — |
Reaction Steps
A batch type process wherein the catalyst compositions are stirred in from 0.01 to 0.5 molar (preferably 0.05 to 0.3 molar) solution of phenylpyruvate in the presence of 0.015 to 0.75 molar ammonium L-aspartate (preferably 0.075 to 0.5 molar) and 0.4 to 0.000001 mmolar pyridoxal 5-phosphate (preferably 0.04 to 0.0004 mmolar in water at 5.0 to 10.0 pH (preferably 7.5 to 9.5 pH) for periods of 1.0 to 100 hours (preferably 8 to 48 hours) at temperatures below 50° C. (preferably 20° to 40° C.). Broadly from 0.05 to 50 g of immobilized cells, preferably from 1.0 to 15 g, are used per 0.1 mole of starting phenylpyruvate. After the conversion, the catalyst compositions may be removed by filtration or the equivalent for reuse in converting fresh batches of phenylpyruvate solutions. The product solutions are obtained in a form suitable for conventional processing to isolate the L-phenylalanine (ion exchange chromotography, precipitation, filtration, washing, recrystallization, drying).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04650755 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-795c3417af074574be9989baebcc5cbf |
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| Source note | uspto-grants-1987_03 |
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