Synthesis of L-phenylalanine analogs by Rhodotorla glutinis. Bioconversion of cinnamic acids derivatives

Synthesis of L-phenylalanine analogs by Rhodotorla glutinis. Bioconversion of cinnamic acids derivatives

The synthesis of L-alpha aromatic amino acids by amination of forty-one derivatives of cinnamic acid and related compounds is tested with the yeast Rhodotorula glutinis.

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Bibliographische Detailangaben
Veröffentlicht in:Biotechnology letters 1992, Vol.14 (8), p.673-678
Hauptverfasser: Renard, G, Guilleux, J.C, Bore, C, Malta-Valette, V, Lerner, D.A
Format: Artikel
Sprache:eng
Schlagworte:
amination
amino acid metabolism
analogs
cinnamic acid
derivatives
phenylalanine
phenylalanine ammonia-lyase
Rhodotorula glutinis
yields
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Zusammenfassung:The synthesis of L-alpha aromatic amino acids by amination of forty-one derivatives of cinnamic acid and related compounds is tested with the yeast Rhodotorula glutinis.
ISSN:0141-5492
1573-6776