Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formate | HCID 283 | — |
| Edukt | DL-alanine | HCID 602 | — |
| Edukt | Pyridoxal 5'-phosphate | HCID 1051 | — |
| Edukt | Lactate | HCID 91435 | — |
| Edukt | Pyruvate | HCID 107735 | — |
| Edukt | Nadh | HCID 439153 | — |
| Edukt | Sodium Formate | HCID 2723810 | — |
| Edukt | 5,5,5-Trifluoro-2-oxopentanoic acid | HCID 14278600 | — |
| Lösungsmittel | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Produkt | (R)-2-Amino-5,5,5-trifluoropentanoic acid | HCID 7177181 | — |
Reaktionsschritte
The yields were increased by adding auxiliary enzymes to reduce pyruvate to lactate. Lactate dehydrogenase requires NADH as a cofactor. The NADH was regenerated using formate dehydrogenase. A solution containing 5,5,5-trifluoro-2-oxopentanoic acid (100 mg, 0.588 mmoles), D,L-alanine (200 mg, 2.244 mmoles), 0.02 mM pyridoxal phosphate, sodium formate (68 mg, 1 mmole), NAD (331 mg, 5 μmoles) L-lactate dehydrogenase cloned from rabbit muscle (Biocatalytics LDH-103, 0.107 mg, 15 units), and formate dehydrogenase (0.5 mL, 15 units cloned from Pichia pastoris and expressed in Escherichia coli) in 0.1 M potassium phosphate buffer, pH 7.5, was incubated with R-transaminase AT-103 from Biocatalytics (5 mg, 44 units) or cloned R-transaminase from Bacillus thuringiensis SC 16569 (0.5 mL, 10 units) at 30° C. in a total volume of 5 mL in 15 mL tubes. Reaction yields of (R)-5,5,5-trifluoro-2-aminopentanoic acid of 94% and 91% were obtained with AT-103 and BMS transaminases, respectively. Ee was 100% in both cases.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08044077B2 |
|---|
| Quelldatensatz | uspto-grants-2011_10 |
|---|
| ORD ID | ord-eecca44b0ee541cc8f84207823d3efdc |
|---|
| Quellennotiz | uspto-grants-2011_10 |
|---|