Indole-3-pyruvic acid → L-Tryptophan

HRID 1106392

Reaktionsgleichung

Reaktionsgleichung von HRID 1106392
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][C:11](=O)[C:12]([OH:14])=[O:13])=[CH:2]1.CC1C(O)=C(CN)C(COP(O)(O)=O)=C[N:18]=1.P([O-])([O-])([O-])=O>O>[NH2:18][C@H:11]([C:12]([OH:14])=[O:13])[CH2:10][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
37 °C

Versuchsvorschrift

To a solution containing 20.3 g (100 mmol) of indole-3-pyruvic acid and 26.5 g (100 mmol) of pyridoxamine-5-phosphate in 1000 ml of distilled water buffered at pH 6.5 with 0.5M phosphate buffer and maintained at 37° C. is added 50 mg of the monoclonal antibodies prepared according to Example 15. The reaction mixture is gently agitated for 2 hours. The monoclonal antibodies are then recovered by ultrafiltration. Dialysis of the reaction mixture followed by lyophilization yields the product L-tryptophan.

Aufarbeitung

  1. additionis added 50 mg of the monoclonal antibodies
  2. customprepared
  3. filtrationThe monoclonal antibodies are then recovered by ultrafiltration
  4. customDialysis of the reaction mixture

Quellen und Nachweise

ORD-Eintrag
ord-50a89337b37942aea5a12499da98f250
Quelldatensatz
uspto-grants-2000_05
Patentnummer
US06057121

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