Ammonium Hydroxide → L-Methionine

HRID 2195601

Reaction equation

HRID 2195601 reaction equation
O=C[C@@H]([C@H:5]([C@@H:7]([C@@H:9]([CH2:11][OH:12])O)O)O)O.OP([O-])([O-])=O.[K+].[K+].Cl.[S:21]1[CH:26]=CC=CC1.OC(CCCC[C@H]1[C@@H]2[C@@H](NC(N2)=O)CS1)=O.[OH-:43].[NH4+:44]>>[NH2:44][C@H:9]([C:11]([OH:12])=[O:43])[CH2:7][CH2:5][S:21][CH3:26]

Participants

6

Procedure

Colonies from agar plates were aseptically transferred into 250 mL flasks containing 30 ml of nutrient broth (DIFCO) and allowed to grow at 30° C. After 24 hours of growth, these microorganisms were used as seed culture in a 3-L fermenter containing growth media consisting of 50 g/L glucose, 50 g/L soy protein hydrolyzate, 1 g/L K2HPO4, 45 g/L (NH4)2SO4, 400 mg/L MgSO4.7H2O, 10 mg/L MnSO4.4H2O, 0.2 mg/L thiamin HCl and 0.05 mg/L biotin. Fermentation was carried out at 31° C. under vigorous agitation and good aeration. pH was maintained at 7.45 during fermentation by addition of ammonium hydroxide (NH4OH). The organisms grew quite well under these conditions with a typical optical density (as measured as OD600) in the range of 25 to 30 after only 24 hours. Fermentation batches were terminated once the initial glucose charge was consumed. The residual L-methionine produced during these fermentations was supplemented with additional L-methionine as described in the Examples below.

Workup

  1. customColonies from agar plates were aseptically transferred into 250 mL flasks
  2. additioncontaining 30 ml of nutrient broth (DIFCO)
  3. customto grow at 30° C
  4. additioncontaining growth media
  5. customwas carried out at 31° C. under vigorous agitation and good aeration
  6. customFermentation batches were terminated once the initial glucose
  7. additioncharge
  8. customwas consumed

Sources & evidence

ORD record
ord-70ee628caaf7488cbb1757f74759aa91
Source dataset
uspto-grants-2012_12
Patent number
US08338141B2

Linked notes

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