期刊
CHEMBIOCHEM
卷 23, 期 15, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.202200335
关键词
amines; biocatalysis; enantioselectivity; enzyme; THF ketones; transaminases
资金
- Biotechnology and Biological Sciences Research Council
- Swiss National Science Foundation (SNSF) [200021_192274]
- Universitat Bern
- Johnson Matthey [BB/M008770/1]
- Swiss National Science Foundation (SNF) [200021_192274] Funding Source: Swiss National Science Foundation (SNF)
This study investigates the importance of enzymatic enantiopreference in biocatalysis, revealing that increasing substrate loadings can lead to the inversion of enantiopreference, and adjusting the ionic strength or co-solvent content in the reaction mixture can alter enantiopreference.
Enzymatic enantiopreference is one of the key advantages of biocatalysis. While exploring the synthesis of small cyclic (chiral amines) such as 3-aminotetrahydrofuran (THF-amine), using the (S)-selective transaminase from Halomonas elongata (HEwT), inversion of the enantiopreference was observed at increasing substrate loadings. In addition, the enantiopreference could be altered by variation of the ionic strength, or of the co-solvent content in the reaction mixture. For example, using otherwise identical reaction conditions, the presence of 2 M sodium chloride gave (R)-THF-amine (14 % ee), while the addition of 2.2 M isopropyl alcohol gave the (S)-enantiomer in 30 % ee. While the underlying cause is not currently understood, it appears likely that subtle changes in the structure of the enzyme cause the shift in enantiopreference and are worth exploring further.
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