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Illuminating the dark metabolome of Pseudo-nitzschia-microbiome associations.
Koester, Irina; Quinlan, Zachary A; Nothias, Louis-Félix; White, Margot E; Rabines, Ariel; Petras, Daniel; Brunson, John K; Dührkop, Kai; Ludwig, Marcus; Böcker, Sebastian; Azam, Farooq; Allen, Andrew E; Dorrestein, Pieter C; Aluwihare, Lihini I.
  • Koester I; Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, USA.
  • Quinlan ZA; Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, USA.
  • Nothias LF; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, California, USA.
  • White ME; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, California, USA.
  • Rabines A; Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, USA.
  • Petras D; Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, USA.
  • Brunson JK; Microbial and Environmental Genomics Group, J. Craig Venter Institute, La Jolla, California, USA.
  • Dührkop K; Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, USA.
  • Ludwig M; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, California, USA.
  • Böcker S; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, California, USA.
  • Azam F; Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, USA.
  • Allen AE; Microbial and Environmental Genomics Group, J. Craig Venter Institute, La Jolla, California, USA.
  • Dorrestein PC; Chair for Bioinformatics, Friedrich Schiller University, Jena, Germany.
  • Aluwihare LI; Chair for Bioinformatics, Friedrich Schiller University, Jena, Germany.
Environ Microbiol ; 24(11): 5408-5424, 2022 11.
Article en En | MEDLINE | ID: mdl-36222155
ABSTRACT
The exchange of metabolites mediates algal and bacterial interactions that maintain ecosystem function. Yet, while thousands of metabolites are produced, only a few molecules have been identified in these associations. Using the ubiquitous microalgae Pseudo-nitzschia sp., as a model, we employed an untargeted metabolomics strategy to assign structural characteristics to the metabolites that distinguished specific diatom-microbiome associations. We cultured five species of Pseudo-nitzschia, including two species that produced the toxin domoic acid, and examined their microbiomes and metabolomes. A total of 4826 molecular features were detected by tandem mass spectrometry. Only 229 of these could be annotated using available mass spectral libraries, but by applying new in silico annotation tools, characterization was expanded to 2710 features. The metabolomes of the Pseudo-nitzschia-microbiome associations were distinct and distinguished by structurally diverse nitrogen compounds, ranging from simple amines and amides to cyclic compounds such as imidazoles, pyrrolidines and lactams. By illuminating the dark metabolomes, this study expands our capacity to discover new chemical targets that facilitate microbial partnerships and uncovers the chemical diversity that underpins algae-bacteria interactions.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diatomeas / Microbiota Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diatomeas / Microbiota Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Año: 2022 Tipo del documento: Article