Enzymatic Thioamide Formation in a Bacterial Antimetabolite Pathway |
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| Authors: | Agnieszka Litomska Dr Keishi Ishida Dr Kyle L Dunbar Marco Boettger Dr Sébastien Coyne Prof Dr Christian Hertweck |
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| Affiliation: | 1. http://www.leibniz‐hki.de;2. Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Chemistry and Infection Biology (HKI), Jena, Germany;3. Faculty of Biological Sciences, Friedrich Schiller University Jena, Jena, Germany |
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| Abstract: | 6‐Thioguanine (6TG) is a DNA‐targeting therapeutic used in the treatment of various cancers. While 6TG was rationally designed as a proof of concept for antimetabolite therapy, it is also a rare thioamide‐bearing bacterial natural product and critical virulence factor of Erwinia amylovorans, plant pathogens that cause fire blight. Through gene expression, biochemical assays, and mutational analyses, we identified a specialized bipartite enzyme system, consisting of an ATP‐dependent sulfur transferase (YcfA) and a sulfur‐mobilizing enzyme (YcfC), that is responsible for the peculiar oxygen‐by‐sulfur substitution found in the biosynthesis of 6TG. Mechanistic and phylogenetic studies revealed that YcfA‐mediated 6TG biosynthesis evolved from ancient tRNA modifications that support translational fidelity. The successful in vitro reconstitution of 6TG thioamidation showed that YcfA employs a specialized sulfur shuttle that markedly differs from universal RNA‐related systems. This study sheds light on underexplored enzymatic C?S bond formation in natural product biosynthesis. |
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| Keywords: | biosynthesis enzymes natural product nucleic acids thioamides |
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