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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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
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container_title Biotechnology letters
container_volume 14
creator Renard, G
Guilleux, J.C
Bore, C
Malta-Valette, V
Lerner, D.A
description 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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1573-6776
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subjects amination
amino acid metabolism
analogs
cinnamic acid
derivatives
phenylalanine
phenylalanine ammonia-lyase
Rhodotorula glutinis
yields
title Synthesis of L-phenylalanine analogs by Rhodotorla glutinis. Bioconversion of cinnamic acids derivatives
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