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Microbial metabolomics in open microscale platforms

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...

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Autores principales: Barkal, Layla J., Theberge, Ashleigh B., Guo, Chun-Jun, Spraker, Joe, Rappert, Lucas, Berthier, Jean, Brakke, Kenneth A., Wang, Clay C. C., Beebe, David J., Keller, Nancy P., Berthier, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742997/
https://www.ncbi.nlm.nih.gov/pubmed/26842393
http://dx.doi.org/10.1038/ncomms10610
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author Barkal, Layla J.
Theberge, Ashleigh B.
Guo, Chun-Jun
Spraker, Joe
Rappert, Lucas
Berthier, Jean
Brakke, Kenneth A.
Wang, Clay C. C.
Beebe, David J.
Keller, Nancy P.
Berthier, Erwin
author_facet Barkal, Layla J.
Theberge, Ashleigh B.
Guo, Chun-Jun
Spraker, Joe
Rappert, Lucas
Berthier, Jean
Brakke, Kenneth A.
Wang, Clay C. C.
Beebe, David J.
Keller, Nancy P.
Berthier, Erwin
author_sort Barkal, Layla J.
collection PubMed
description 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.
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spelling pubmed-47429972016-03-04 Microbial metabolomics in open microscale platforms Barkal, Layla J. Theberge, Ashleigh B. Guo, Chun-Jun Spraker, Joe Rappert, Lucas Berthier, Jean Brakke, Kenneth A. Wang, Clay C. C. Beebe, David J. Keller, Nancy P. Berthier, Erwin Nat Commun Article 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. Nature Publishing Group 2016-02-04 /pmc/articles/PMC4742997/ /pubmed/26842393 http://dx.doi.org/10.1038/ncomms10610 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Barkal, Layla J.
Theberge, Ashleigh B.
Guo, Chun-Jun
Spraker, Joe
Rappert, Lucas
Berthier, Jean
Brakke, Kenneth A.
Wang, Clay C. C.
Beebe, David J.
Keller, Nancy P.
Berthier, Erwin
Microbial metabolomics in open microscale platforms
title Microbial metabolomics in open microscale platforms
title_full Microbial metabolomics in open microscale platforms
title_fullStr Microbial metabolomics in open microscale platforms
title_full_unstemmed Microbial metabolomics in open microscale platforms
title_short Microbial metabolomics in open microscale platforms
title_sort microbial metabolomics in open microscale platforms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742997/
https://www.ncbi.nlm.nih.gov/pubmed/26842393
http://dx.doi.org/10.1038/ncomms10610
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