HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tris(hydroxymethyl)aminomethane → Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | Isobutyric Acid | HCID 6590 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Lactic Acid | HCID 107689 | — |
| Reactant | Hydroxyacetate | HCID 5460308 | — |
| Product | Acetate | HCID 175 | — |
| Product | Pyruvate | HCID 107735 | — |
Reaction Steps
The procedure described in Comparative Example A was repeated using a 10 mL aqueous solution containing L-lactic acid (96% L-isomer, 4% D-isomer, 0.750M total), FMN (0.01 mM), isobutyric acid (HPLC internal standard, 0.100M), Tris buffer (0.750M), soluble spinach glycolate oxidase (1.0 IU/mL), and soluble Aspergillus niger catalase (1,400 IU/mL) at pH 8.3 (adjusted with 50% NaOH) and the reaction run at 5° C. After 39 hours, the HPLC yields of pyruvate and acetate were 55.1% and 6.3%, respectively, and 2.7% lactate remained. The remaining activity of glycolate oxidase and catalase were 29% and 94%, respectively, of their initial values.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538875 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-4374dfef7a734e3a95aad4b50f86cbe5 |
| Source note | uspto-grants-1996_07 |