Reconstitution of Iterative Thioamidation in Closthioamide Biosynthesis Reveals Tailoring Strategy for Nonribosomal Peptide Backbones
Abstract: Thioamide‐containing nonribosomal peptides (NRPs) are exceedingly rare. Recently the biosynthetic gene cluster for the thioamidated NRP antibiotic closthioamide (CTA) was reported, however, the enzyme responsible for and the timing of thioamide formation remained enigmatic. Here, genome editing, biochemical assays, and mutational studies are used to demonstrate that an Fe‐S cluster containing member of the adenine nucleotide α‐hydrolase protein superfamily (CtaC) is responsible for sulfur incorporation during CTA biosynthesis. However, unlike all previously characterized members, CtaC functions in a thiotemplated manner. In addition to prompting a revision of the CTA biosynthetic pathway, the reconstitution of CtaC provides the first example of a NRP thioamide synthetase. Finally, CtaC is used as a bioinformatic handle to demonstrate that thioamidated NRP biosynthetic gene clusters are more widespread than previously appreciated.
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Reconstitution of Iterative Thioamidation in Closthioamide Biosynthesis Reveals Tailoring Strategy for Nonribosomal Peptide Backbones ; volume:131 ; number:37 ; year:2019 ; pages:13148-13152 ; extent:5
Angewandte Chemie ; 131, Heft 37 (2019), 13148-13152 (gesamt 5)
- Creator
- DOI
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10.1002/ange.201905992
- URN
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urn:nbn:de:101:1-2022080106494757619203
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:24 AM CEST
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Associated
- Dunbar, Kyle L.
- Dell, Maria
- Molloy, Evelyn M.
- Kloss, Florian
- Hertweck, Christian
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Funktionalisierte Vinyloxirane durch reduktive Allylierung von Estern : stereoselektive Synthesen von Lamoxiren und Sphingoidbasen
Expanding the toolbox for engineering nonribosomal peptide synthetases
Photosensitizers Enable the Formation of Biphenyls with UV‐LEDs and Sunlight
Novel Biocatalysts from Specialized Metabolism
Novel Biocatalysts from Specialized Metabolism
Loss of Single‐Domain Function in a Modular Assembly Line Alters the Size and Shape of a Complex Polyketide
A Photochemical Macrocyclization Route to Asymmetric Strained (3.2) Paracyclophanes
Bacterial Isothiocyanate Biosynthesis by Rhodanese‐Catalyzed Sulfur Transfer onto Isonitriles
A Type III Polyketide Synthase Specific for Sporulating Negativicutes is Responsible for Alkylpyrone Biosynthesis
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Reconstitution of Iterative Thioamidation in Closthioamide Biosynthesis Reveals Tailoring Strategy for Nonribosomal Peptide Backbones
Funktionalisierte Vinyloxirane durch reduktive Allylierung von Estern : stereoselektive Synthesen von Lamoxiren und Sphingoidbasen
Expanding the toolbox for engineering nonribosomal peptide synthetases
Photosensitizers Enable the Formation of Biphenyls with UV‐LEDs and Sunlight
Novel Biocatalysts from Specialized Metabolism
Novel Biocatalysts from Specialized Metabolism
Loss of Single‐Domain Function in a Modular Assembly Line Alters the Size and Shape of a Complex Polyketide
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