Identification of a newly isolated Sphingomonas sp. LZ1 and its application to biosynthesize chiral alcohols
Author:
Affiliation:
1. School of Life Science, Hunan University of Science and Technology
2. Hunan Key Laboratory of Economic Crops Genetic Improvement and Integrated Utilization
Publisher
Microbiology Research Foundation
Subject
Applied Microbiology and Biotechnology,Microbiology
Link
https://www.jstage.jst.go.jp/article/jgam/66/5/66_2019.12.002/_pdf
Reference28 articles.
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2. Cui, Z. M., Zhang, J. D., Fan, X. J., Zheng, G. W., Chang, H. H. et al. (2017) Highly efficient bioreduction of 2-hydroxyacetophenone to (S)- and (R)-1-phenyl-1,2-ethanediol by two substrate tolerance carbonyl reductases with cofactor regeneration. J. Biotechnol., 243, 1–9.
3. Dascier, D., Kambourakis, S., Hua, L., Rozzell, J. D., and Stewart, J. D. (2014) Influence of cofactor regeneration strategies on preparative-scale, asymmetric carbonyl reductions by engineered Escherichia coli. Org. Process Res. Dev., 18, 793–800.
4. Gai, P., Tang, C. G., Liu, J. Y., Liu, Y., Zhang, C. et al. (2013) Asymmetric anti-Prelog reduction of 3,5-bis(trifluoromethyl)-acetophenone by Microbacterium oxydans C3. Chin. J. Appl. Environ. Biol., 19, 37–42.
5. Homann, M. J., Vail, R. B., Previte, E., Tamarez, M., Morgan, B. et al. (2004) Rapid identification of enantioselective ketone reductions using targeted microbial libraries. Tetrahedron, 60, 789–797.
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