Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenylacetic Acid | HCID 999 | — |
| Edukt | Penicillin G | HCID 5904 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | p-Dimethylaminobenzaldehyde methanol | HCID 20437094 | — |
| Edukt | Penicillin G Potassium | HCID 23664709 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Phosphate | HCID 1061 | — |
| Produkt | 6-Aminopenicillanic acid | HCID 11082 | — |
Reaktionsschritte
An amount of penicillin acylase enzyme, either free or immobilized on the carrier, sufficient to contain about 50 I.U. of activity, was suspended in 60 ml of 7.5-pH phosphate buffer. The mixture was maintained at 28° C. in a vessel connected to a pH controller which electrometrically determined the pH and metered in sufficient 0.8 N sodium hydroxide solution to maintain the pH at approximately 8.0. A solution containing 5 g of penicillin G potassium salt in phosphate buffer, also at 28° C., was added to the vessel, and the rate of formation of phenylacetic acid by the enzyme-catalyzed hydrolysis of the penicillin G was determined from the rate of addition of sodium hydroxide solution to maintain the pH. The liquid in the vessel was sampled upon addition of the penicillin G salt and after 10 and 30 minutes. These samples (0.5 ml) were immediately mixed with 3 ml of a solution of 1 ml of 0.05 M sodium hydroxide, 2 ml of 20% acetic acid and 0.5% (weight-volume) p-dimethylaminobenzaldehyde/methanol, and were allowed to stand for 10 minutes. The amount of 6-aminopenicillanic acid formed was determined by spectrophotometrically measuring the light absorption of the mixture at a wave length of 415 nm.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04612288 |
|---|
| Quelldatensatz | uspto-grants-1986_09 |
|---|
| ORD ID | ord-720609f0e522413ab8f16c30b91add24 |
|---|
| Quellennotiz | uspto-grants-1986_09 |
|---|