Whole cell biotransformation for reductive amination reactions

Klatte S, Lorenz E, Wendisch VF (2014)
BioEngineered 5(1): 56-62.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
Autor*in
Klatte, StephanieUniBi; Lorenz, ElisabethUniBi; Wendisch, Volker F.UniBi
Einrichtung
Fakultät für Biologie > Genetik der Prokaryoten
Centrum für Biotechnologie > Arbeitsgruppe V. Wendisch
Erscheinungsjahr
2014
Zeitschriftentitel
BioEngineered
Band
5
Ausgabe
1
Seite(n)
56-62
ISSN
2165-5979
eISSN
2165-5987
Page URI
https://pub.uni-bielefeld.de/record/2634007

Zitieren

Klatte S, Lorenz E, Wendisch VF. Whole cell biotransformation for reductive amination reactions. BioEngineered. 2014;5(1):56-62.
Klatte, S., Lorenz, E., & Wendisch, V. F. (2014). Whole cell biotransformation for reductive amination reactions. BioEngineered, 5(1), 56-62. doi:10.4161/bioe.27151
Klatte, Stephanie, Lorenz, Elisabeth, and Wendisch, Volker F. 2014. “Whole cell biotransformation for reductive amination reactions”. BioEngineered 5 (1): 56-62.
Klatte, S., Lorenz, E., and Wendisch, V. F. (2014). Whole cell biotransformation for reductive amination reactions. BioEngineered 5, 56-62.
Klatte, S., Lorenz, E., & Wendisch, V.F., 2014. Whole cell biotransformation for reductive amination reactions. BioEngineered, 5(1), p 56-62.
S. Klatte, E. Lorenz, and V.F. Wendisch, “Whole cell biotransformation for reductive amination reactions”, BioEngineered, vol. 5, 2014, pp. 56-62.
Klatte, S., Lorenz, E., Wendisch, V.F.: Whole cell biotransformation for reductive amination reactions. BioEngineered. 5, 56-62 (2014).
Klatte, Stephanie, Lorenz, Elisabeth, and Wendisch, Volker F. “Whole cell biotransformation for reductive amination reactions”. BioEngineered 5.1 (2014): 56-62.

5 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Biotechnological production of mono- and diamines using bacteria: recent progress, applications, and perspectives.
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Metabolic Engineering of Raoultella ornithinolytica BF60 for Production of 2,5-Furandicarboxylic Acid from 5-Hydroxymethylfurfural.
Hossain GS, Yuan H, Li J, Shin HD, Wang M, Du G, Chen J, Liu L., Appl Environ Microbiol 83(1), 2017
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Palacio CM, Crismaru CG, Bartsch S, Navickas V, Ditrich K, Breuer M, Abu R, Woodley JM, Baldenius K, Wu B, Janssen DB., Biotechnol Bioeng 113(9), 2016
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Construction of a tunable multi-enzyme-coordinate expression system for biosynthesis of chiral drug intermediates.
Jiang W, Fang B., Sci Rep 6(), 2016
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A synthetic biology approach for the transformation of l-α-amino acids to the corresponding enantiopure (R)- or (S)-α-hydroxy acids.
Gourinchas G, Busto E, Killinger M, Richter N, Wiltschi B, Kroutil W., Chem Commun (Camb) 51(14), 2015
PMID: 25574527

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