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Diketopiperazine Formation in Fungi Requires Dedicated Cyclization and Thiolation Domains.


ABSTRACT: Cyclization of linear dipeptidyl precursors derived from nonribosomal peptide synthetases (NRPSs) into 2,5-diketopiperazines (DKPs) is a crucial step in the biosynthesis of a large number of bioactive natural products. However, the mechanism of DKP formation in fungi has remained unclear, despite extensive studies of their biosyntheses. Here we show that DKP formation en route to the fungal virulence factor gliotoxin requires a seemingly extraneous couplet of condensation (C) and thiolation (T) domains in the NRPS GliP. In vivo truncation of GliP to remove the CT couplet or just the T domain abrogated production of gliotoxin and all other gli pathway metabolites. Point mutation of conserved active sites in the C and T domains diminished cyclization activity of GliP in vitro and abolished gliotoxin biosynthesis in vivo. Verified NRPSs of other fungal DKPs terminate with similar CT domain couplets, suggesting a conserved strategy for DKP biosynthesis by fungal NRPSs.

SUBMITTER: Baccile JA 

PROVIDER: S-EPMC6764874 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Diketopiperazine Formation in Fungi Requires Dedicated Cyclization and Thiolation Domains.

Baccile Joshua A JA   Le Henry H HH   Pfannenstiel Brandon T BT   Bok Jin Woo JW   Gomez Christian C   Brandenburger Eileen E   Hoffmeister Dirk D   Keller Nancy P NP   Schroeder Frank C FC  

Angewandte Chemie (International ed. in English) 20190828 41


Cyclization of linear dipeptidyl precursors derived from nonribosomal peptide synthetases (NRPSs) into 2,5-diketopiperazines (DKPs) is a crucial step in the biosynthesis of a large number of bioactive natural products. However, the mechanism of DKP formation in fungi has remained unclear, despite extensive studies of their biosyntheses. Here we show that DKP formation en route to the fungal virulence factor gliotoxin requires a seemingly extraneous couplet of condensation (C) and thiolation (T)  ...[more]

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