Mixing and Matching of Hybrid Megasynthases is a Hub for the Evolution of Metabolic Diversity in Cyanobacteria

Modular megasynthases, such as polyketide synthases (PKSs) and nonribosomal peptide synthetases (NRPSs), are molecular assembly lines that biosynthesize many pharmaceutically and ecologically important natural products. Understanding how these compounds evolve could inspire the artificial evolution of compound diversity by metabolic engineering. Over the past two decades, a number of seminal studies have significantly contributed to our understanding of natural product evolution. However, the evolution of NRPS and PKS assembly lines remains poorly understood, especially for NRPS/PKS hybrids. Here, we provide substantial evidence for a remarkable cluster-mixing event involving three cyanobacterial biosynthetic gene clusters (BGCs), resulting in the emergence of novel peptide-polyketide hybrids that were named minutumamides. By combining retro-evolutionary analysis with structure-guided genome mining, we could discover a potential evolutionary ancestor that links nostopeptolide and minutumamide biosynthesis. In addition, we were able to trace nostopeptolide-related module and domain blocks in various other biosynthetic pathways, indicating a surprisingly vivid mixing and matching of biosynthesis genes in the evolution of NRPS and cis-acyltransferase PKS/NRPS pathways, which was previously regarded as a unique feature of trans-acyltransferase (trans-AT) PKS. These remarkable insights into the evolutionary plasticity of NRPS-PKS assembly lines provide valuable guidance for pathway engineers looking for productive combinations that yield "nonnatural" hybrid natural products.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-04-17
DOI
https://doi.org/10.1002/anie.202502461
Citations
3
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
4.18

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article

Mixing and Matching of Hybrid Megasynthases is a Hub for the Evolution of Metabolic Diversity in Cyanobacteria

Elke Dittmann, Martin Baunach, Jonna E. Teikari, Christian Hertweck et al.
3 citations
Angewandte Chemie International Edition
Microbial Natural Products and Biosynthesis
4.18
article

Mixing and Matching of Hybrid Megasynthases is a Hub for the Evolution of Metabolic Diversity in Cyanobacteria

Elke Dittmann, Martin Baunach, Jonna E. Teikari, Christian Hertweck, Masahiro Murakami, Qi Sun, Keishi Ishida
article en
3 citations

Abstract

Modular megasynthases, such as polyketide synthases (PKSs) and nonribosomal peptide synthetases (NRPSs), are molecular assembly lines that biosynthesize many pharmaceutically and ecologically important natural products. Understanding how these compounds evolve could inspire the artificial evolution of compound diversity by metabolic engineering. Over the past two decades, a number of seminal studies have significantly contributed to our understanding of natural product evolution. However, the evolution of NRPS and PKS assembly lines remains poorly understood, especially for NRPS/PKS hybrids. Here, we provide substantial evidence for a remarkable cluster-mixing event involving three cyanobacterial biosynthetic gene clusters (BGCs), resulting in the emergence of novel peptide-polyketide hybrids that were named minutumamides. By combining retro-evolutionary analysis with structure-guided genome mining, we could discover a potential evolutionary ancestor that links nostopeptolide and minutumamide biosynthesis. In addition, we were able to trace nostopeptolide-related module and domain blocks in various other biosynthetic pathways, indicating a surprisingly vivid mixing and matching of biosynthesis genes in the evolution of NRPS and cis-acyltransferase PKS/NRPS pathways, which was previously regarded as a unique feature of trans-acyltransferase (trans-AT) PKS. These remarkable insights into the evolutionary plasticity of NRPS-PKS assembly lines provide valuable guidance for pathway engineers looking for productive combinations that yield "nonnatural" hybrid natural products.

Angewandte Chemie International EditionVol. 64(26)
University of Helsinki (FI), University of Bonn (DE), University of Potsdam (DE), Helsinki Institute of Physics (FI), Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) (DE), The University of Tokyo (JP), Friedrich Schiller University Jena (DE)
Deutsche Forschungsgemeinschaft
Responsible consumption and production
Openalex Percentile: Top 7%
Microbial Natural Products and Biosynthesis
4.18
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