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The Biosynthetic Logic of Polyketide Diversity
Abstract
Molecular Lego: Polyketides represent a highly diverse group of natural products with structurally intriguing carbon skeletons (see picture) which are assembled from simple acyl building blocks. A combination of chemical, biochemical, and genetics studies have provided exciting new insights into the programming of polyketide assembly and the sophisticated enzymatic machineries involved. This review highlights recent developments in the field.magnified image Polyketides constitute one of the major classes of natural products. Many of these compounds or derivatives thereof have become important therapeutics for clinical use; in contrast, various polyketides are infamous food‐spoiling toxins or virulence factors. What is particularly remarkable about this heterogeneous group of compounds comprising of polyethers, polyenes, polyphenols, macrolides, and enediynes is that they are mainly derived from one of the simplest building blocks available in nature: acetic acid. Investigations at the chemical, genetic, and biochemical levels have shed light on the biosynthetic programs that lead to the large structural diversity of polyketides .This review highlights recently unveiled biosynthetic mechanisms to generate highly diverse and complex molecules.
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Cites
RifamycinMode of Action, Resistance, and Biosynthesis
Floss, H. G., & Yu, T.-W. (2005) · Chemical Reviews · doi:10.1021/cr030112j · Cited by 547
Cited by
Rocha-Martin, J., Harrington, C., Dobson, A., & O'Gara, F. (2014) · Marine Drugs · doi:10.3390/md12063516 · Cited by 84
Combining Stable Isotope Labeling and Molecular Networking for Biosynthetic Pathway Characterization
Klitgaard, A., Nielsen, J. B., Frandsen, R. J. N., Andersen, M. R., & Nielsen, K. F. (2015) · Analytical Chemistry · doi:10.1021/acs.analchem.5b01934 · Cited by 54
Docking Domain Engineering in a Modular Polyketide Synthase and Its Impact on Structure and Function
Buyachuihan, L., Zhao, Y., Schelhas, C., & Grininger, M. (2023) · ACS Chemical Biology · doi:10.1021/acschembio.3c00074 · Cited by 15
Repurposing a Fully Reducing Polyketide Synthase toward 2-Methyl Guerbet-like Lipids
Herrera, M. A., McColm, S., Craigie, L.-M., Simpson, J., Brown, F., Clarke, D. J., Carr, R., & Campopiano, D. J. (2024) · ACS Catalysis · doi:10.1021/acscatal.4c04714 · Cited by 1
Metadata
- Authors
- Hertweck, C.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2009-06-09
- Volume
- 48
- Issue
- 26
- Pages
- 4688-4716
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2159489517
- Cited by
- 1,346
- References
- 1
- FWCI
- 38.63
- Type
- journal article
- Language
- en
- Open access
- closed
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