Literature DB >> 7858980

Enzyme-catalysed enantioselective hydrolysis of racemic naproxen nitrile.

F Effenberger1, J Böhme.   

Abstract

The bacterial strain Rhodococcus butanica (ATCC 21197), which exhibits nitrilase and nitrile hydratase/amidase activities, catalyses the enantioselective hydrolysis of racemic naproxen nitrile (R/S)-1 to furnish a moderate enantiomeric excess of (S)-naproxen (S)-3. Racemic naproxen amide (R/S)-2 is not a good substrate for this strain. Resting cells of the newly selected bacterial strain Rhodococcus sp. C3II catalyse the enantioselective hydrolyses of racemic naproxen nitrile (R/S)-1 and naproxen amide (R/S)-2 as well, to give (S)-3 in excellent optical (99% e.e.) and good chemical yields in aqueous medium and in the biphasic system of phosphate buffer/hexane.

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Year:  1994        PMID: 7858980     DOI: 10.1016/0968-0896(94)85022-4

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  2 in total

1.  Enzymatic production of 2-amino-2,3-dimethylbutyramide by cyanide-resistant nitrile hydratase.

Authors:  Zhi-Jian Lin; Ren-Chao Zheng; Ya-Jun Wang; Yu-Guo Zheng; Yin-Chu Shen
Journal:  J Ind Microbiol Biotechnol       Date:  2011-07-02       Impact factor: 3.346

2.  Production of R-(-)-Ketoprofen from an Amide Compound by Comamonas acidovorans KPO-2771-4.

Authors:  K Yamamoto; K Otsubo; A Matsuo; T Hayashi; I Fujimatsu; K Komatsu
Journal:  Appl Environ Microbiol       Date:  1996-01       Impact factor: 4.792

  2 in total

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