Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | 2-Propenoic acid, 3-phenyl- | HCID 8784 | — |
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Reactant | Methylene-bisacrylamide | HCID 53800990 | — |
| Solvent | Water | HCID 962 | — |
| Product | L-Phenylalanine | HCID 6140 | — |
Reaction Steps
One gram of microbial cells of Syncephalastrum racemosum IFO-4814, grown by the method described in Example 1, and one gram each of microbial cells of AJ-117128 (FERM P-7736, FERM BP-693) and AJ-6307 (FERM P-7892, FERM BP-694) grown by the method described in Example 2, were each suspended in 4 ml of deionized water. After cooling on ice, 750 mg of acrylamide and 45 mg of methylene-bisacrylamide were dissolved in each suspension, the oxygen was completely displaced by introducing nitrogen gas, 3.5 mg of ammonium persulfate and 8 μl of N,N'-dimethylaminopropionitrile were added, and the mixture was allowed to stand under ice cooling. After one hour, the cell-containing gel thus formed was collected by filtration through a 50-mesh metal gauze and washed with physiological saline. Two grams of the immobilized cells thus obtained were added to an aqueous solution containing 2.0 g/dl of cinnamic acid and 5.5 ml of 28% ammonia (pH controlled to 10.5 with hydrochloric acid), and the reaction was continued at 30° C. for 24 hours. The amounts of phenylalanine formed are listed in Table 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04755466 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-26c4bfd9d3a4404ba83c8727f184954e |
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| Source note | uspto-grants-1988_07 |
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