Bioinformatic, phylogenetic and chemical analysis of the UV‐absorbing compounds scytonemin and mycosporine‐like amino acids from the microbial mat communities of Shark Bay, Australia

  • Paul M. D'Agostino
    School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney New South Wales Australia
  • Jason N. Woodhouse
    School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney New South Wales Australia
  • Heng Tai Liew
    School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney New South Wales Australia
  • Luděk Sehnal
    Research Centre for Toxic Compounds in the Environment, Faculty of Science Masaryk University Kamenice 5, 625 00, Brno Czech Republic
  • Russel Pickford
    Bioanalytical Mass Spectrometry Facility, Mark Wainwright Analytical Centre University of New South Wales Sydney New South Wales Australia
  • Hon Lun Wong
    School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney New South Wales Australia
  • Brendan P. Burns
    School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney New South Wales Australia
  • Brett A. Neilan
    School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney New South Wales Australia

説明

<jats:title>Summary</jats:title><jats:p>Shark Bay, Western Australia is a World Heritage area with extensive microbial mats and stromatolites. Microbial communities that comprise these mats have developed a range of mitigation strategies against changing levels of photosynthetically active and ultraviolet radiation, including the ability to biosynthesise the UV‐absorbing natural products scytonemin and mycosporine‐like amino acids (MAAs). To this end, the distribution of photoprotective pigments within Shark Bay microbial mats was delineated in the present study. This involved amplicon sequencing of bacterial 16S rDNA from communities at the surface and subsurface in three distinct mat types (smooth, pustular and tufted), and correlating this data with the chemical and molecular distribution of scytonemin and MAAs. Employing UV spectroscopy and MS/MS fragmentation, mycosporine‐glycine, asterina and an unknown MAA were identified based on typical fragmentation patterns. Marker genes for scytonemin and MAA production (<jats:italic>scyC</jats:italic> and <jats:italic>mysC</jats:italic>) were amplified from microbial mat DNA and placed into phylogenetic context against a broad screen throughout 363 cyanobacterial genomes. Results indicate that occurrence of UV screening compounds is associated with the upper layer of Shark Bay microbial mats, and the occurrence of scytonemin is closely dependent on the abundance of cyanobacteria.</jats:p>

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