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Abstract
A comparison of substrate-binding site amino acid residues in the C-methyltransferase (MT) domains of fungal nonreducing polyketide synthases (NR-PKSs) suggests that these residues are correlated with the methylation modes used by the PKSs. A PKS, designated as AsbPKS, with substrate-binding site residues distinct from those of other known PKSs is focused on. The characterization of AsbPKS revealed that it yields an isocoumarin derivative, anhydrosclerotinin B (1), the biosynthesis of which involves a previously unreported methylation pattern. This study demonstrates the utility of MT domain-focused genome mining for the discovery of PKSs with new functions. © 2024 The Authors. Small Methods published by Wiley-VCH GmbH.
| Original language | English |
|---|---|
| Article number | 2400107 |
| Journal | Small Methods |
| Volume | 8 |
| Issue number | 11 |
| Online published | 21 Apr 2024 |
| DOIs | |
| Publication status | Published - 20 Nov 2024 |
Funding
This work was supported by a General Research Fund grant from the Research Grants Council of Hong Kong (Project No. 11301321).
Research Keywords
- biosynthesis
- methyltransferase domains
- natural products
- polyketide synthases
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
RGC Funding Information
- RGC-funded
Fingerprint
Dive into the research topics of 'Methyltransferase Domain-Focused Genome Mining for Fungal Polyketide Synthases'. Together they form a unique fingerprint.Projects
- 1 Finished
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GRF: Broadening the Chemical Space of Fungal Meroterpenoids and the Enzymatic Repertoire for Their Biosynthesis
MATSUDA, Y. (Principal Investigator / Project Coordinator)
1/01/22 → 15/12/25
Project: Research
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