Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Tromethamine hydrochloride | HCID 93573 | — |
| Reactant | Pterin | HCID 135398660 | — |
| Solvent | 2-amino-6,6-dimethyl-1,5,7,8-tetrahydropteridin-4-one | HCID 178428361 | — |
| Product | L-Tyrosine | HCID 6057 | — |
Reaction Steps
Absorbance Spectrum of Quinoid-6,6-Me2PH2Generated by Phenylalanine Hydroxylase. Spectra were taken of the q-6,6-Me2PH2 synthesized enzymatically from 6,6-Me2PH4, and a comparison made with the chemically produced compound. The spectrophotometer was baseline corrected with sample and reference cuvettes containing all of the reaction components (0.1M Tris·HCl, pH 7.4, 4 mM phenylalanine, 2500 units catalase, 0.3 unit phenylalanine hydroxylase) except pterin in a total volume of 0.99 ml. 6,6-Me2PH4 (10 μl of 10 mM) was then added to the sample and distilled H2O (10 μl) to the reference cuvette. Scanning was begun immediately and spectra taken at 2 minute intervals. The formation of q-6,6-Me2PH2 was complete within 4 minutes. After correction for tyrosine formed and phenylalanine consumed, the spectrum was within 3% of that produced by Br2 oxidation of 6,6-Me2PH4 (FIGURE).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401844 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-a42c435ce5e9469ebaddcb6a3e0cf4b7 |
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| Source note | uspto-grants-1995_03 |
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