Abstract

Type III polyketide synthases (PKSs) produce secondary metabolites with diverse biological activities, including antimicrobials. While they have been extensively studied in plants and bacteria, only a handful of type III PKSs from fungi has been characterized in the last 15 years. The exploitation of fungal type III PKSs to produce novel bioactive compounds requires understanding the diversity of these enzymes, as well as of their biosynthetic pathways. Here, phylogenetic and reconciliation analyses of 522 type III PKSs from 1,193 fungal genomes revealed complex evolutionary histories with massive gene duplications and losses, explaining their discontinuous distribution in the fungal tree of life. In addition, horizontal gene transfer events from bacteria to fungi and, to a lower extent, between fungi, could be inferred. Ancestral gene duplication events have resulted in the divergence of eight phylogenetic clades. Especially, two clades show ancestral linkage and functional co-evolution between a type III PKS and a reducing PKS genes. Investigation of the occurrence of protein domains in fungal type III PKS predicted gene clusters highlighted the diversity of biosynthetic pathways, likely reflecting a large chemical landscape. Type III PKS genes are most often located next to genes encoding cytochrome P450s, MFS transporters and transcription factors, defining ancestral core gene clusters. This analysis also allowed predicting gene clusters for the characterized fungal type III PKSs and provides working hypotheses for the elucidation of the full biosynthetic pathways. Altogether, our analyses provide the fundamental knowledge to motivate further characterization and exploitation of fungal type III PKS biosynthetic pathways.

Highlights

  • The genomic era has revealed that fungal genomes carry many more biosynthetic pathways than known compounds, demonstrating that the fungal kingdom has been an underexploited resource of secondary metabolites (SMs)

  • Fungal type III polyketide synthases (PKSs) protein sequences were retrieved from 1,193 fungal genomes available at the JGI Mycocosm repository (Grigoriev et al, 2014)

  • A total of 522 type III PKSs were found in only 407 fungal species (34% of all included genomes), 318 of these species carrying a single sequence and 89 having between two and five copies (Supplementary Tables S1–S3)

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Summary

Introduction

The genomic era has revealed that fungal genomes carry many more biosynthetic pathways than known compounds, demonstrating that the fungal kingdom has been an underexploited resource of secondary metabolites (SMs). Access to this hidden biodiversity is hampered by the strict regulation of SM biosynthetic pathways under specific conditions that are difficult to reproduce in the laboratory (Keller, 2019). Fungal Type III PKS Evolution (Keller, 2019). Type I iterative PKSs are multidomain megaenzymes that are responsible for the production of most fungal polyketide compounds (Herbst et al, 2018). While type I PKSs have been well characterized and found to be abundant in fungal genomes, only a handful of fungal type III PKSs have been characterized so far (Hashimoto et al, 2014; Sun et al, 2016; Ramakrishnan et al, 2018; Yan et al, 2018; Kaneko et al, 2019; Manoharan et al, 2019)

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