Abstract

Cyanobacteria are an ancient lineage of slow-growing photosynthetic bacteria and a prolific source of natural products with diverse chemical structures and potent biological activities and toxicities. The chemical identification of these compounds remains a major bottleneck. Strategies that can prioritize the most prolific strains and novel compounds are of great interest. Here, we combine chemical analysis and genomics to investigate the chemodiversity of secondary metabolites based on their pattern of distribution within some cyanobacteria. Planktothrix being a cyanobacterial genus known to form blooms worldwide and to produce a broad spectrum of toxins and other bioactive compounds, we applied this combined approach on four closely related strains of Planktothrix. The chemical diversity of the metabolites produced by the four strains was evaluated using an untargeted metabolomics strategy with high-resolution LC–MS. Metabolite profiles were correlated with the potential of metabolite production identified by genomics for the different strains. Although, the Planktothrix strains present a global similarity in terms of a biosynthetic cluster gene for microcystin, aeruginosin, and prenylagaramide for example, we found remarkable strain-specific chemodiversity. Only few of the chemical features were common to the four studied strains. Additionally, the MS/MS data were analyzed using Global Natural Products Social Molecular Networking (GNPS) to identify molecular families of the same biosynthetic origin. In conclusion, we depict an efficient, integrative strategy for elucidating the chemical diversity of a given genus and link the data obtained from analytical chemistry to biosynthetic genes of cyanobacteria.

Highlights

  • Cyanobacteria are an ancient lineage of bacteria that colonize a broad range of habitats, from soil to oceans, and play important roles in the global nitrogen and carbon cycles [1]

  • The four strains of Planktothrix were selected on their green (Pasteur Culture of Cyanobacteria (PCC) 10110, PCC 7805, and NIVA CYA 126/8) vs. red (PCC 7821) morphotypes and their characteristics to produce (PCC 10110, PCC 7821, and NIVA CYA 126/8) or not (PCC 7805) microcystins (Table S1)

  • Our results demonstrate the efficiency of the Global Natural Products Social Molecular Networking (GNPS)-based analysis of the global chemical diversity of Planktothrix metabolites, that remarkably represent a large set of cyclic or non-cyclic peptides biosynthesized by RIPP or polyketide synthase (PKS)/non-ribosomal peptide synthetase (NRPS) pathways

Read more

Summary

Introduction

Cyanobacteria are an ancient lineage of bacteria that colonize a broad range of habitats, from soil to oceans, and play important roles in the global nitrogen and carbon cycles [1] They are well known for the production of toxins, and to form toxic blooms in freshwater bodies around the world, posing a threat to human health [2,3,4]. Isolated by means of traditional bioactivity-guided screening techniques [8], these compounds present promising therapeutic potential, with anticancer, multidrug-reversing, antifungal, antibacterial, anti-inflammatory, antiviral, and potent enzyme-inhibiting bioactivities [9,10] These molecules can be respectively assigned to a diverse panel of structural classes, including peptides, polyketides, alkaloids, lipids, and terpenes [10,11]. These complex metabolites are commonly synthesized on enzymatic assembly lines of non-ribosomal and ribosomal biosynthetic pathways namely the non-ribosomal peptide synthetase (NRPS) and the polyketide synthase (PKS) enzyme systems [12], or the ribosomally synthesized and post-translationally modified peptide (RiPP) pathways [13]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call