Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridoxal 5'-phosphate | HCID 1051 | — |
| Reactant | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Reactant | L-Tyrosine | HCID 6057 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | Tyrosine phenol | HCID 67207896 | — |
Reaction Steps
The plasmids pTK919 [pSC101 ori, bla::tet, tyrR] and pTK922 [pSC101 ori, bla::tet, tyrR V67A, Y72C, E201G] obtained as described above were introduced into the YG17 strain to obtain the YG38 strain and the YG40 strain, respectively. These strains were cultured overnight at 30° C. in 100 ml of the basal medium containing 0.1% tyrosine. The microbial cells were suspended in 10 mM potassium phosphate buffer (pH 7.0), 0.2 mM PLP (pyridoxal 5′-phosphate), 5 mM 2-mercaptoethnol and 4 mM EDTA (pH 7.0) and disrupted by sonication. The suspension containing the disrupted microbial cells was dialyzed against the buffer overnight. The amount of protein and tyrosine phenol lyase activity in the crude enzyme solution obtained as described above were determined.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933365B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-da99b7641dac4d0382cb967f32db3301 |
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| Source note | uspto-grants-2005_08 |
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