Summary of Study ST001880
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.
Study ID | ST001880 |
Study Title | NMR Predator Cues Target Signaling Pathways in Toxic Algal Metabolome (Polar metabolites) |
Study Type | 1H NMR Metabolomics to elucidate signaling pathway |
Study Summary | Metabolomics 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 |
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, Georgia USA 30332 |
julia.kubanek@biosci.gatech.edu | |
Phone | 404-894-8424 |
Submit Date | 2021-07-15 |
Num Groups | 2 |
Total Subjects | 40 |
Study Comments | Part 1 of 3. This part includes NMR analysis of polar metabolites using oPLSDA. Parts 2 and 3 inlcude NMR analysis of nonpolar metabolites and the corresponding mass spectrometry metabolomics for both polar and non-polar metabolites. |
Raw Data Available | Yes |
Raw Data File Type(s) | fid |
Analysis Type Detail | NMR |
Release Date | 2021-07-27 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
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 |
Subject:
Subject ID: | SU001960 |
Subject Type: | Other organism |
Subject Species: | Alexandrium minutum |
Taxonomy ID: | 39455 |
Genotype Strain: | CCMP 113 |
Gender: | Not applicable |
Factors:
Subject type: Other organism; Subject species: Alexandrium minutum (Factor headings shown in green)
mb_sample_id | local_sample_id | Treatment |
---|---|---|
SA175050 | Control 16 | Control |
SA175051 | Control 14 | Control |
SA175052 | Control 13 | Control |
SA175053 | Control 17 | Control |
SA175054 | Control 19 | Control |
SA175055 | Control 1 | Control |
SA175056 | Control 20 | Control |
SA175057 | Control 12 | Control |
SA175058 | Control 18 | Control |
SA175059 | Control 15 | Control |
SA175060 | Control 5 | Control |
SA175061 | Control 4 | Control |
SA175062 | Control 11 | Control |
SA175063 | Control 2 | Control |
SA175064 | Control 6 | Control |
SA175065 | Control 3 | Control |
SA175066 | Control 7 | Control |
SA175067 | Control 10 | Control |
SA175068 | Control 9 | Control |
SA175069 | Control 8 | Control |
SA175070 | Copepodamide 15 | Copepodamide |
SA175071 | Copepodamide 14 | Copepodamide |
SA175072 | Copepodamide 13 | Copepodamide |
SA175073 | Copepodamide 16 | Copepodamide |
SA175074 | Copepodamide 19 | Copepodamide |
SA175075 | Copepodamide 12 | Copepodamide |
SA175076 | Copepodamide 20 | Copepodamide |
SA175077 | Copepodamide 18 | Copepodamide |
SA175078 | Copepodamide 17 | Copepodamide |
SA175079 | Copepodamide 1 | Copepodamide |
SA175080 | Copepodamide 5 | Copepodamide |
SA175081 | Copepodamide 4 | Copepodamide |
SA175082 | Copepodamide 3 | Copepodamide |
SA175083 | Copepodamide 2 | Copepodamide |
SA175084 | Copepodamide 6 | Copepodamide |
SA175085 | Copepodamide 7 | Copepodamide |
SA175086 | Copepodamide 10 | Copepodamide |
SA175087 | Copepodamide 9 | Copepodamide |
SA175088 | Copepodamide 8 | Copepodamide |
SA175089 | Copepodamide 11 | Copepodamide |
Showing results 1 to 40 of 40 |
Collection:
Collection ID: | CO001953 |
Collection Summary: | Alexandrium minutum cells were collected by vacuum filtration onto GF/F filters and quenched with liquid nitrogen. Frozen cells with filters were stored in foil (previously muffled for 3 h at 450 °C) at -80 °C until extraction. |
Collection Protocol Filename: | Predator_Cues_Target_Signaling_Pathways_in_Toxic_Algal_Metabolome_protocol.pdf |
Sample Type: | Algae |
Collection Method: | Filtration and Freeze |
Storage Conditions: | -80℃ |
Treatment:
Treatment ID: | TR001972 |
Treatment Summary: | Twice, first at the start of the experiment and again 24 h later, 1.5 mL of either 0.2 µM copepodamides (copepod cue) in DMSO (treatment, n=20) or DMSO alone (control, n=20) were added aseptically to 300 mL cultures of Alexandrium minutum resulting in a final concentration of 1 nM copepodamides. |
Treatment Protocol Filename: | Predator_Cues_Target_Signaling_Pathways_in_Toxic_Algal_Metabolome_protocol.pdf |
Sample Preparation:
Sampleprep ID: | SP001966 |
Sampleprep Summary: | Polar extracts were dissolved at a concentration equivalent to 1.70 x 10^7 A. minutum cells mL-1 in 90:10 H2O/D2O (99.96% atom D2O; Cambridge Isotope Labs) with 0.2 mM phosphate buffer (pH 7.4) and 0.25 mM 3 (trimethylsilyl)propionic 2,2,3,3d 4 acid (TMSP), as internal standard, for 1H NMR spectroscopy analysis. The media blank extract was prepared in the smallest volume of solvent possible (175 µL). Particulates were excluded by briefly centrifuging the samples and then carefully transferring the extracts into 3 mm NMR tubes. The extracts were analyzed using a Bruker Avance IIIHD 800 MHz NMR spectrometer equipped with a 3 mm triple resonance broadband cryoprobe. Spectra for the polar extracts were acquired using a 1D water presaturation (Bruker zgpr pulse sequence) with a spectral width of 12 kHz centered at 3758.36 Hz, with a relaxation delay 3 s, over 480 scans. |
Sampleprep Protocol Filename: | Predator Cues Target Signaling Pathways in Toxic Algal Metabolome_protocol.pdf |
Extract Storage: | -80℃ |
Analysis:
Analysis ID: | AN003046 |
Analysis Type: | NMR |
Results File: | Preprocessed_binned_polar_NMRmetabolomics.txt |
Units: | area under the curve |
NMR:
NMR ID: | NM000211 |
Analysis ID: | AN003046 |
Instrument Name: | Bruker Avance IIIHD |
Instrument Type: | FT-NMR |
NMR Experiment Type: | 1D-1H |
Spectrometer Frequency: | 800 MHz |
NMR Probe: | 3 mm triple resonance broadband cryoprobe |
NMR Solvent: | 90:10 H2O/D2O (99.96% atom D2O; Cambridge Isotope Labs) with 0.2 mM phosphate buffer (pH 7.4) and 0.25 mM 3-(trimethylsilyl)propionic-2,2,3,3d4-acid |
NMR Tube Size: | 3 mm |
Pulse Sequence: | zgpr |
Number Of Scans: | 480 |
Relaxation Delay: | 3s |
Spectral Width: | 12 kHz |
Baseline Correction Method: | Spline |
Binned Increment: | 0.005 ppm |