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Identification of Novel α-Pyrones from Conexibacter woesei Serving as Sulfate Shuttles.
- Source :
-
ACS chemical biology [ACS Chem Biol] 2019 Sep 20; Vol. 14 (9), pp. 1972-1980. Date of Electronic Publication: 2019 Aug 27. - Publication Year :
- 2019
-
Abstract
- Pyrones comprise a structurally diverse class of compounds. Although they are widespread in nature, their specific physiological functions remain unknown in most cases. We recently described that triketide pyrones mediate the sulfotransfer in caprazamycin biosynthesis. Herein, we report the identification of conexipyrones A-C, three previously unrecognized tetra-substituted α-pyrones, from the soil actinobacterium Conexibacter woesei . Insights into their biosynthesis via a type III polyketide synthase were obtained by feeding studies using isotope-enriched precursors. In vitro assays employing the genetically associated 3'-phosphoadenosine-5'-phosphosulfate (PAPS)-dependent sulfotransferase CwoeST revealed conexipyrones as the enzymes' genuine sulfate acceptor substrates. Furthermore, conexipyrones were determined to function as sulfate shuttles in a two-enzyme assay, because their sulfated derivatives were accepted as donor molecules by the PAPS-independent arylsulfate sulfotransferase (ASST) Cpz4 to yield sulfated caprazamycin intermediates.
- Subjects :
- Arylsulfotransferase metabolism
Bacterial Proteins genetics
Bacterial Proteins metabolism
Phosphoadenosine Phosphosulfate metabolism
Polyketide Synthases genetics
Pyrones isolation & purification
Streptomyces coelicolor genetics
Actinobacteria chemistry
Pyrones metabolism
Sulfuric Acid Esters metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1554-8937
- Volume :
- 14
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- ACS chemical biology
- Publication Type :
- Academic Journal
- Accession number :
- 31419109
- Full Text :
- https://doi.org/10.1021/acschembio.9b00455