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Microbial metabolomics in open microscale platforms

Author

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  • Layla J. Barkal

    (University of Wisconsin-Madison
    Carbone Cancer Center, University of Wisconsin-Madison)

  • Ashleigh B. Theberge

    (University of Wisconsin-Madison
    Carbone Cancer Center, University of Wisconsin-Madison
    University of Wisconsin-Madison)

  • Chun-Jun Guo

    (University of Southern California)

  • Joe Spraker

    (University of Wisconsin-Madison)

  • Lucas Rappert

    (University of Wisconsin-Madison)

  • Jean Berthier

    (CEA-University Grenoble-Alpes)

  • Kenneth A. Brakke

    (Susquehanna University)

  • Clay C. C. Wang

    (University of Southern California
    University of Southern California)

  • David J. Beebe

    (University of Wisconsin-Madison
    Carbone Cancer Center, University of Wisconsin-Madison)

  • Nancy P. Keller

    (University of Wisconsin-Madison
    University of Wisconsin-Madison)

  • Erwin Berthier

    (University of Wisconsin-Madison
    Carbone Cancer Center, University of Wisconsin-Madison)

Abstract

The microbial secondary metabolome encompasses great synthetic diversity, empowering microbes to tune their chemical responses to changing microenvironments. Traditional metabolomics methods are ill-equipped to probe a wide variety of environments or environmental dynamics. Here we introduce a class of microscale culture platforms to analyse chemical diversity of fungal and bacterial secondary metabolomes. By leveraging stable biphasic interfaces to integrate microculture with small molecule isolation via liquid–liquid extraction, we enable metabolomics-scale analysis using mass spectrometry. This platform facilitates exploration of culture microenvironments (including rare media typically inaccessible using established methods), unusual organic solvents for metabolite isolation and microbial mutants. Utilizing Aspergillus, a fungal genus known for its rich secondary metabolism, we characterize the effects of culture geometry and growth matrix on secondary metabolism, highlighting the potential use of microscale systems to unlock unknown or cryptic secondary metabolites for natural products discovery. Finally, we demonstrate the potential for this class of microfluidic systems to study interkingdom communication between fungi and bacteria.

Suggested Citation

  • Layla J. Barkal & Ashleigh B. Theberge & Chun-Jun Guo & Joe Spraker & Lucas Rappert & Jean Berthier & Kenneth A. Brakke & Clay C. C. Wang & David J. Beebe & Nancy P. Keller & Erwin Berthier, 2016. "Microbial metabolomics in open microscale platforms," Nature Communications, Nature, vol. 7(1), pages 1-11, April.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10610
    DOI: 10.1038/ncomms10610
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