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Recent Advances in Discovery, Structure, Bioactivity, and Biosynthesis of trans -AT Polyketides.
- Source :
-
Journal of agricultural and food chemistry [J Agric Food Chem] 2024 Oct 02; Vol. 72 (39), pp. 21318-21343. Date of Electronic Publication: 2024 Sep 20. - Publication Year :
- 2024
-
Abstract
- Bacterial trans -acyltransferase polyketide synthases ( trans -AT PKSs) are among the most complex enzymes, which are responsible for generating a wide range of natural products, identified as trans -AT polyketides. These polyketides have received significant attention in drug development due to their structural diversity and potent bioactivities. With approximately 300 synthesized molecules discovered so far, trans -AT PKSs are found widespread in bacteria. Their biosynthesis pathways exhibit considerable genetic diversity, leading to the emergence of numerous enzymes with novel mechanisms, serving as a valuable resource for genetic engineering aimed at modifying small molecules' structures and creating new engineered enzymes. Despite the systematic discussions on trans -AT polyketides and their biosynthesis in earlier studies, the continuous advancements in tools, methods, compound identification, and biosynthetic pathways require a fresh update on accumulated knowledge. This review seeks to provide a comprehensive discussion for the 27 types of trans -AT polyketides discovered within the last seven years, detailing their sources, structures, biological activities, and biosynthetic pathways. By reviewing this new knowledge, a more profound understanding of the trans -AT polyketide family can be achieved.
- Subjects :
- Bacterial Proteins metabolism
Bacterial Proteins genetics
Bacterial Proteins chemistry
Drug Discovery
Humans
Polyketides metabolism
Polyketides chemistry
Polyketide Synthases metabolism
Polyketide Synthases genetics
Polyketide Synthases chemistry
Bacteria metabolism
Bacteria genetics
Bacteria enzymology
Biosynthetic Pathways
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5118
- Volume :
- 72
- Issue :
- 39
- Database :
- MEDLINE
- Journal :
- Journal of agricultural and food chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 39302874
- Full Text :
- https://doi.org/10.1021/acs.jafc.4c03750