反応式
C1N=C(N)C2N=CN([C@@H]3O[C@H](COP(OP(OC[C@H]4O[C@@H](N5C=C(C(N)=O)CC=C5)[C@H](O)[C@@H]4O)(O)=O)(O)=O)[C@@H](O)[C@H]3O)C=2N=1.[CH3:45][N+:46]([CH2:49][C:50]([CH2:52][C:53]([OH:55])=[O:54])=[O:51])([CH3:48])[CH3:47].[Cl-]>>[OH:51][C@H:50]([CH2:52][C:53](=[O:54])[O-:55])[CH2:49][N+:46]([CH3:48])([CH3:45])[CH3:47]参加物
実験手順
Carnitine dehydrogenase obtained as in example 1 was used in that synthesis. Synthesis of L-carnitine was carried out in the same conditions as in example 1, except as concerns the NADH regeneration system which was the yeast alcohol dehydrogenase and ethanol system instead of the glucose dehydrogenase and glucose system. Glucose was thus substituted with ethanol (concentration in the reactor: 4% by volume) and glucose dehydrogenase with 4 mg (700 units) of purified yeast alcohol dehydrogenase (Sigma ref. A 3263). Nitrogen was bubbled through the reactor (80 ml/mn) to eliminate the acetaldehyde formed by alcohol oxidation and thus improve the NADH regeneration. After 30 h, 0.325 g of L-carnitine was produced from dehydrocarnitine hydrochloride with a yield of 27%.
出典と根拠
- ORDレコード
- ord-34f8bce2d0be46169f37fee9c1cb5f13
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04221869
関連ノート
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