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Unnatural biosynthesis by an engineered microorganism with heterologously expressed natural enzymes and an artificial metalloenzyme.
- Source :
-
Nature chemistry [Nat Chem] 2021 Dec; Vol. 13 (12), pp. 1186-1191. Date of Electronic Publication: 2021 Oct 14. - Publication Year :
- 2021
-
Abstract
- Synthetic biology enables microbial hosts to produce complex molecules from organisms that are rare or difficult to cultivate, but the structures of these molecules are limited to those formed by reactions of natural enzymes. The integration of artificial metalloenzymes (ArMs) that catalyse unnatural reactions into metabolic networks could broaden the cache of molecules produced biosynthetically. Here we report an engineered microbial cell expressing a heterologous biosynthetic pathway, containing both natural enzymes and ArMs, that produces an unnatural product with high diastereoselectivity. We engineered Escherichia coli with a heterologous terpene biosynthetic pathway and an ArM containing an iridium-porphyrin complex that was transported into the cell with a heterologous transport system. We improved the diastereoselectivity and product titre of the unnatural product by evolving the ArM and selecting the appropriate gene induction and cultivation conditions. This work shows that synthetic biology and synthetic chemistry can produce, by combining natural and artificial enzymes in whole cells, molecules that were previously inaccessible to nature.<br /> (© 2021. The Author(s), under exclusive licence to Springer Nature Limited.)
- Subjects :
- Bacterial Proteins chemistry
Bacterial Proteins genetics
Cytochrome P-450 Enzyme System chemistry
Cytochrome P-450 Enzyme System genetics
Escherichia coli genetics
Escherichia coli metabolism
Iridium chemistry
Mesoporphyrins chemistry
Metabolic Engineering
Stereoisomerism
Sulfolobus solfataricus enzymology
Terpenes chemistry
Bacterial Proteins metabolism
Cytochrome P-450 Enzyme System metabolism
Terpenes metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1755-4349
- Volume :
- 13
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Nature chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 34650235
- Full Text :
- https://doi.org/10.1038/s41557-021-00801-3