Related Experiment Video
Updated: Jul 20, 2026

Isolation of Culturable Yeasts and Molds from Soils to Investigate Fungal Population Structure
Published on: May 27, 2022
Phylogenomic analysis of non-ribosomal peptide synthetases in the genus Aspergillus
Robert A Cramer1, Jason E Stajich, Yvonne Yamanaka
1Duke University Medical Center, Department of Molecular Genetics and Microbiology, Durham, NC 27710, USA. rcramer@duke.edu
Abstract:
Fungi from the genus Aspergillus are important saprophytes and opportunistic human fungal pathogens that contribute in these and other diverse ways to human well-being. Part of their impact on human well-being stems from the production of small molecular weight secondary metabolites, which may contribute to the ability of these fungi to cause invasive fungal infections and allergic diseases. In this study, we identified one group of enzymes responsible for secondary metabolite production in five Aspergillus species, the non-ribosomal peptide synthetases (NRPS). Hidden Markov models were used to search the genome databases of A. fumigatus, A. flavus, A. terreus, A. nidulans, and A. oryzae for domains conserved in NRPS proteins. A genealogy of adenylation domains was utilized to identify orthologous and unique NRPS among the Aspergillus species examined, as well as gain an understanding of the potential evolution of Aspergillus NRPS. mRNA abundance of the 14 NRPS identified in the A. fumigatus genome was analyzed using real-time reverse transcriptase PCR in different environmental conditions to gain a preliminary understanding of the possible functions of the NRPSs' peptide products. Our results suggest that Aspergillus species contain conserved and unique NRPS genes with a complex evolutionary history. This result suggests that the genus Aspergillus produces a substantial diversity of non-ribosomally synthesized peptides. Further analysis of these genes and their peptide products may identify important roles for secondary metabolites produced by NRPS in Aspergillus physiology, ecology, and fungal pathogenicity.
Insights
Aspergillus fungi produce diverse secondary metabolites via non-ribosomal peptide synthetases (NRPS). This study reveals conserved and unique NRPS genes across five Aspergillus species, suggesting complex evolution and varied peptide products.
Area of Science:
- Mycology
- Biochemistry
- Genomics
Background:
- * Fungi in the genus *Aspergillus* are significant saprophytes and opportunistic human pathogens.
- * Their impact on human health is partly due to secondary metabolites, which can cause invasive infections and allergies.
- * Non-ribosomal peptide synthetases (NRPS) are key enzymes in producing these metabolites.
Purpose of the Study:
- * To identify and characterize NRPS enzymes across five *Aspergillus* species.
- * To understand the evolutionary history of NRPS genes within the *Aspergillus* genus.
- * To explore the potential functions of NRPS-derived peptides in *A. fumigatus*.
Main Methods:
- * Genome-wide searches using Hidden Markov Models to identify NRPS domains.
- * Phylogenetic analysis of adenylation domains to determine orthology and evolutionary relationships.
- * Real-time reverse transcriptase PCR to quantify NRPS mRNA abundance in *A. fumigatus* under various conditions.
Main Results:
- * Identification of conserved and unique NRPS genes across *A. fumigatus*, *A. flavus*, *A. terreus*, *A. nidulans*, and *A. oryzae*.
- * Evidence of a complex evolutionary history for *Aspergillus* NRPS.
- * *A. fumigatus* possesses 14 NRPS genes, with varying mRNA abundance suggesting diverse functional roles.
Conclusions:
- * *Aspergillus* species harbor a substantial diversity of NRPS genes.
- * These genes exhibit conserved and unique features, indicating complex evolutionary trajectories.
- * Further research into NRPS and their products is crucial for understanding *Aspergillus* biology, ecology, and pathogenicity.
Related Concept Videos
Fungal Phylum Ascomycota
Bacterial Phylum Actinobacteria
Microbial Phylogeny
Amino Acid Biosynthetic Pathways
Evolutionary Relationships through Genome Comparisons
Sulfur Assimilation
