Summary of Study ST001881

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001186. The data can be accessed directly via it's Project DOI: 10.21228/M8DD61 This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST001881
Study TitleNMR Predator Cues Target Signaling Pathways in Toxic Algal Metabolome (Non-polar metabolites)
Study Type1H NMR Metabolomics to elucidate signaling pathway
Study SummaryMetabolomics investigation of the phytoplankton Alexandrium minutum with and without copepod cues in order to explore cell signaling involved in toxin induction.
Institute
Georgia Institute of Technology
DepartmentSchool of Biological Sciences, School of Chemistry and Biochemistry, Center for Microbial Dynamics and Infection, Parker H. Petit Institute for Bioengineering and Bioscience
LaboratoryKubanek Lab
Last NameBrown
First NameEmily
Address950 Atlantic Dr Atlanta, Georgia USA 30332
Emailjulia.kubanek@biosci.gatech.edu
Phone404-894-8424
Submit Date2021-07-19
Num Groups2
Total Subjects40
Study CommentsPart 2 of 3. This part includes NMR analysis of non-polar metabolites using oPLSDA. Parts 1 and 3 inlcude NMR analysis of polar metabolites and the corresponding mass spectrometry metabolomics for both polar and non-polar metabolites.
Raw Data AvailableYes
Raw Data File Type(s)fid
Analysis Type DetailNMR
Release Date2021-07-27
Release Version1
Emily Brown Emily Brown
https://dx.doi.org/10.21228/M8DD61
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001186
Project DOI:doi: 10.21228/M8DD61
Project Title:Predator Cues Target Signaling Pathways in Toxic Algal Metabolome
Project Type:Metabolomics to elucidate signaling pathway
Project Summary:Early detection of predators is critical to the survival of all living organisms. For phytoplankton, recognition and response to chemical cues from predators, as evidence of predation risk, is particularly crucial. The phytoplankton Alexandrium minutum upregulates its toxicity when exposed to copepodamides, a suite of compounds released by copepod predators. However, how A. minutum perceives these predatory cues and what metabolic pathways are involved in initiating toxin induction remains unknown. In this study LC/MS and NMR-based metabolomics uncovered subtle physiological responses of A. minutum to copepodamides, including dysregulation of valine biosynthesis and enhancement of butanoate metabolism and arginine biosynthesis. While we have yet to identify a chemoreceptor directly activated by copepod cues, based on the results of inhibition experiments detection of copepodamides appears to disrupt the activity of serine/threonine phosphatases leading to increased jasmonic acid biosynthesis and signaling, which leads to amplified gonyautoxin biosynthesis in A. minutum. This study is an important step toward a better understanding of chemosensory ecology of predator-prey interactions in phytoplankton.
Institute:Georgia Institute of Technology
Department:School of Biological Sciences, School of Chemistry and Biochemistry, Center for Microbial Dynamics and Infection, Parker H. Petit Institute for Bioengineering and Bioscience
Laboratory:Kubanek Lab
Last Name:Brown
First Name:Emily
Address:950 Atlantic Dr Atlanta, GA, 30332, USA
Email:julia.kubanek@biosci.gatech.edu
Phone:404-894-8424
Project Comments:This study has 3 parts: 2 NMR (polar and non-polar metabolites) and MS
Contributors:Emily R. Brown, Sam G. Moore, David A. Gaul, and Julia Kubanek
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