Abstract
Hyper-thermostable aminotransferase from Thermococcus profundus (MsAT) was used to synthesize 3-(2-naphthyl)-l-alanine (Nal) by transamination between its corresponding α-keto acid, 3-(2-naphthyl)pyruvate (NPA) and l-glutamate (Glu) at 70 °C. Equilibrium of this reaction was shifted toward Nal production due to its low solubility, giving rise to Nal precipitate. Optically pure Nal (>99% ee) was synthesized with 93% (mol mol−1) yield from 180 mM NPA and 360 mM Glu.
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Kawashima Y, Fujimura K, Suhara H, Miyawaki N, Fujita Y (1996) 1,3-Dialkylurea derivatives having a hydroxyl group. WO Patent Number 96/14293.
Kobayashi T (1997) Functional analysis of a novel multi-substrate aminotransferase. Program and Abstracts of The 5th Anniversary Novo Nordisk Enzyme Symposium, pp. 21-26.
Lesson PA, Rabasseda X, Castaner J (1997) FK-888. Drugs Future 22: 353-358.
Meiwes J, Schudok M, Kretzschmar G (1997) Asymmetric synthesis of L-thienylalanines. Tetrahedron Asym. 8: 827-536.
Rozzel JD (1987) Immobilized aminotransferase for amino acid production. Meth. Enzymol. 136: 479-497.
Schulz A, Taggeselle R, Tripier D, Bartsch K (1990) Stereospecific production of the herbicide phosphinothricin (Glufosinate) by transamination: isolation and characterization of a phosphinothricin-specific transaminase from Escherichia coli. Appl. Environ. Microbiol. 56: 1-6.
Then J, Barthsch K, Deger H, Grabley S, Marquardt R (1987) Verfahren zur Herstellung von L-tertiär-Leucin durch Transamierung. EP Patent Number 0,533,216 A1.
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Hanzawa, S., Oe, S., Tokuhisa, K. et al. Chemo-enzymatic synthesis of 3-(2-naphthyl)- L-alanine by an aminotransferase from the extreme thermophile, Thermococcus profundus. Biotechnology Letters 23, 589–591 (2001). https://doi.org/10.1023/A:1010308506263
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DOI: https://doi.org/10.1023/A:1010308506263