Unique Biosynthetic Pathway in Bloom-Forming Cyanobacterial Genus Microcystis Jointly Assembles Cytotoxic Aeruginoguanidines and Microguanidines.
Claire PancraceKeishi IshidaEnora BriandDouglas Gatte PichiAnnika R WeizArthur GuljamowThibault ScalvenziNathalie SassoonChristian HertweckElke DittmannMuriel GuggerPublished in: ACS chemical biology (2018)
The cyanobacterial genus Microcystis is known to produce an elaborate array of structurally unique and biologically active natural products, including hazardous cyanotoxins. Cytotoxic aeruginoguanidines represent a yet unexplored family of peptides featuring a trisubstituted benzene unit and farnesylated arginine derivatives. In this study, we aimed at assigning these compounds to a biosynthetic gene cluster by utilizing biosynthetic attributes deduced from public genomes of Microcystis and the sporadic distribution of the metabolite in axenic strains of the Pasteur Culture Collection of Cyanobacteria. By integrating genome mining with untargeted metabolomics using liquid chromatography with mass spectrometry, we linked aeruginoguanidine (AGD) to a nonribosomal peptide synthetase gene cluster and coassigned a significantly smaller product to this pathway, microguanidine (MGD), previously only reported from two Microcystis blooms. Further, a new intermediate class of compounds named microguanidine amides was uncovered, thereby further enlarging this compound family. The comparison of structurally divergent AGDs and MGDs reveals an outstanding versatility of this biosynthetic pathway and provides insights into the assembly of the two compound subfamilies. Strikingly, aeruginoguanidines and microguanidines were found to be as widespread as the hepatotoxic microcystins, but the occurrence of both toxin families appeared to be mutually exclusive.
Keyphrases
- mass spectrometry
- liquid chromatography
- high resolution mass spectrometry
- genome wide
- escherichia coli
- high resolution
- tandem mass spectrometry
- healthcare
- gas chromatography
- copy number
- high performance liquid chromatography
- risk assessment
- mental health
- simultaneous determination
- nitric oxide
- emergency department
- amino acid
- late onset
- gene expression
- ms ms
- electronic health record