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Literature DB >> 21487615

Kinetic resolution of aromatic β-amino acids by ω-transaminase.

Han-Seop Bea¹, Hye-Jeong Park, Sang-Hyeup Lee, Hyungdon Yun.

Abstract

Racemic aromatic β-amino acids have been kinetically resolved into (R)-β-amino acids with high enantiomeric excess (>99%) by a novel ω-TA with ca. 50% conversion. © The Royal Society of Chemistry 2011

Entities: Chemical

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Year: 2011 PMID： 21487615 DOI： 10.1039/c1cc11528f

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

7 in total

1. Structural determinants of the β-selectivity of a bacterial aminotransferase.

Authors: Gjalt G Wybenga; Ciprian G Crismaru; Dick B Janssen; Bauke W Dijkstra
Journal: J Biol Chem Date: 2012-06-28 Impact factor: 5.157

2. Biochemical properties and crystal structure of a β-phenylalanine aminotransferase from Variovorax paradoxus.

Authors: Ciprian G Crismaru; Gjalt G Wybenga; Wiktor Szymanski; Hein J Wijma; Bian Wu; Sebastian Bartsch; Stefaan de Wildeman; Gerrit J Poelarends; Ben L Feringa; Bauke W Dijkstra; Dick B Janssen
Journal: Appl Environ Microbiol Date: 2012-10-19 Impact factor: 4.792

3. Asymmetric Preparation of prim-, sec-, and tert-Amines Employing Selected Biocatalysts.

Authors: Wolfgang Kroutil; Eva-Maria Fischereder; Christine S Fuchs; Horst Lechner; Francesco G Mutti; Desiree Pressnitz; Aashrita Rajagopalan; Johann H Sattler; Robert C Simon; Elina Siirola
Journal: Org Process Res Dev Date: 2013-04-22 Impact factor: 3.317

Kinetic resolution of aromatic β-amino acids by ω-transaminase.

1. Structural determinants of the β-selectivity of a bacterial aminotransferase.

2. Biochemical properties and crystal structure of a β-phenylalanine aminotransferase from Variovorax paradoxus.

3. Asymmetric Preparation of prim-, sec-, and tert-Amines Employing Selected Biocatalysts.

Review 4. Transaminases for industrial biocatalysis: novel enzyme discovery.

5. Exploiting cell metabolism for biocatalytic whole-cell transamination by recombinant Saccharomyces cerevisiae.

6. Construction of a tunable multi-enzyme-coordinate expression system for biosynthesis of chiral drug intermediates.

7. Concise Chemoenzymatic Three Step Total Synthesis of Isosolenopsin Through Medium Engineering.