Expanding chemistry through in vitro and in vivo biocatalysis
- PMID: 38961155
- DOI: 10.1038/s41586-024-07506-w
Expanding chemistry through in vitro and in vivo biocatalysis
Abstract
Living systems contain a vast network of metabolic reactions, providing a wealth of enzymes and cells as potential biocatalysts for chemical processes. The properties of protein and cell biocatalysts-high selectivity, the ability to control reaction sequence and operation in environmentally benign conditions-offer approaches to produce molecules at high efficiency while lowering the cost and environmental impact of industrial chemistry. Furthermore, biocatalysis offers the opportunity to generate chemical structures and functions that may be inaccessible to chemical synthesis. Here we consider developments in enzymes, biosynthetic pathways and cellular engineering that enable their use in catalysis for new chemistry and beyond.
© 2024. Springer Nature Limited.
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References
-
- Hönig, M., Sondermann, P., Turner, N. J. & Carreira, E. M. Enantioselective chemo- and biocatalysis: partners in retrosynthesis. Angew. Chem. Int. Ed. 56, 8942–8973 (2017). - DOI
-
- Romero, E. et al. Enzymatic late-stage modifications: better late than never. Angew. Chem. Int. Ed. 60, 16824–16855 (2021). - DOI
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