Carbon–Carbon Bond-Forming Enzymes for the Synthesis of Non-natural Amino Acids
Author:
Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-61779-331-8_5.pdf
Reference23 articles.
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2. Liu JQ, Odani M, Yasuoka T, et al. (2000) Gene cloning and overproduction of low-specificity D-threonine aldolase from Alcaligenes xylosoxidans and its application for production of a key intermediate for parkinsonism drug. Appl Microbiol Biotechnol 54, 44–51.
3. Liu JQ, Odani M, Dairi T, et al. (1999) A new route to L-threo-3-[4-(methylthio)phenylserine], a key intermediate for the synthesis of antibiotics: recombinant low-specificity D-threonine aldolase-catalyzed stereospecific resolution. Appl Microbiol Biotechnol 51, 586–591.
4. Herbert RB, Wilkinson B, Ellames GJ, et al. (1993) Stereospecific lysis of a range of β-hydroxy-α-amino acids catalyzed by a novel aldolase from Streptomyces amakusaensis. Chem Commun 205–206.
5. Machajewski TD, and Wong C-H (2000) The catalytic asymmetric aldol reaction. Angew Chem Int Ed 39, 1353–1374.
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