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Advisor(s)
Abstract(s)
Two novel natural products, the polyketide cuniculene and the peptide antibiotic aquimarin,
were recently discovered from the marine bacterial genus Aquimarina. However, the diversity of the
secondary metabolite biosynthetic gene clusters (SM-BGCs) in Aquimarina genomes indicates a far
greater biosynthetic potential. In this study, nine representative Aquimarina strains were tested for
antimicrobial activity against diverse human-pathogenic and marine microorganisms and subjected
to metabolomic and genomic profiling. We found an inhibitory activity of most Aquimarina strains
against Candida glabrata and marine Vibrio and Alphaproteobacteria species. Aquimarina sp. Aq135 and
Aquimarina muelleri crude extracts showed particularly promising antimicrobial activities, amongst
others against methicillin-resistant Staphylococcus aureus. The metabolomic and functional genomic
profiles of Aquimarina spp. followed similar patterns and were shaped by phylogeny. SM-BGC and
metabolomics networks suggest the presence of novel polyketides and peptides, including cyclic
depsipeptide-related compounds. Moreover, exploration of the ‘Sponge Microbiome Project’ dataset
revealed that Aquimarina spp. possess low-abundance distributions worldwide across multiple
marine biotopes. Our study emphasizes the relevance of this member of the microbial rare biosphere
as a promising source of novel natural products. We predict that future metabologenomics studies of
Aquimarina species will expand the spectrum of known secondary metabolites and bioactivities from
marine ecosystems.
Description
Keywords
Bioactivity screening Biosynthetic gene clusters Metabolic networks Microbial diversity Natural products The Sponge Microbiome Project
Citation
Marine Drugs 20 (7): 423 (2022)
Publisher
MDPI