Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845013Generated: October 30, 2026

Ammonia → L-Phenylalanine

https://huagongshe.com/reaction/845013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantOxygenHCID 977—
ReactantAcrylamideHCID 6579—
Reactant2-Propenoic acid, 3-phenyl-HCID 8784—
ReactantAmmonium PersulfateHCID 62648—
ReactantMethylene-bisacrylamideHCID 53800990—
SolventWaterHCID 962—
ProductL-PhenylalanineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04755466
Source datasetuspto-grants-1988_07
ORD IDord-26c4bfd9d3a4404ba83c8727f184954e
Source noteuspto-grants-1988_07