Strategic single point mutation yields a solvent- and salt-stable transaminase from Virgibacillus sp. in soluble form
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-34434-3.pdf
Reference37 articles.
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2. Slabu, I., Galman, J. L., Richard, C., Lloyd, R. C. & Turner, N. J. Discovery, engineering, and synthetic application of transaminase biocatalysts. ACS Catal. 7, 8263–8284 (2017).
3. Gomm, A. & O'Reilly, E. Transaminases for chiral amine synthesis. Curr. Opin. Chem. Biol. 43, 106–112 (2018).
4. Ferrandi, E. E. & Monti, D. Amine transaminases in chiral amines synthesis: recent advances and challenges. World J. Microbiol. Biotechnol. 34, 13–23 (2018).
5. Savile, C. K. et al. Biocatalytic asymmetric synthesis of chiral amines from ketones applied to Sitagliptin manufacture. Science 329, 305–309 (2010).
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