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Updated: Sep 26, 2026

From a Natural Product to Its Biosynthetic Gene Cluster: A Demonstration Using Polyketomycin from Streptomyces diastatochromogenes Tü6028
Published on: January 13, 2017
Comparative Phylogenomics Reveals Conserved Protoilludene Synthase Neighbourhoods and Unevenly Distributed
Huijun Su1, Ming Luo1, Yuhuan Miao1,2
1School of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, China.
Abstract:
Fungal biosynthetic gene clusters (BGCs) offer a genomic entry point for natural-product discovery, but predicted regions alone neither establish pathway activity nor identify metabolites. Armillaria is a useful model because chemically rich, forest-associated species span pathogenic and saprotrophic lifestyles. We analysed nine assemblies in a role-aware design: seven independent taxa with high completeness assessed using Benchmarking Universal Single-Copy Orthologs (BUSCO), an A. mellea BUSCO duplication-sensitivity sample and an A. solidipes intraspecific strain control for A. ostoyae. The analysis resolved a terpene-rich repertoire containing a shared but edge-robust gene cluster family (GCF) component alongside unevenly distributed candidate families. Targeted neighbourhood analysis recovered protoilludene synthase (PRO1) orthologs in all assemblies (92.2-100.0% amino-acid identity); the core neighbourhood was retained across the seven primary taxa, whereas flanking tailoring-associated genes varied. Notably, the A. gallica PRO1 ortholog lay 23,614 bp outside the nearest antiSMASH region. Thus, whole-region prediction can obscure pathway-centred conservation in basidiomycetes. The resulting framework prioritises reproducible candidates while reserving chemical identity, expression and ecological function for direct validation.
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