Summary of Study ST000103
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 PR000095. The data can be accessed directly via it's Project DOI: 10.21228/M8S88T This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST000103 |
Study Title | 2D-INADEQUATE NMR study of C. elegans metabolome |
Study Type | Heats Shock Worms |
Study Summary | 2D INADEQUATE NMR datasets were collected from the endo and exo metabolome of heat shocked and control C. elegans |
Institute | University of Florida |
Department | Department of Biochemistry and Molecular Biology and Southeastern Center for Integrated Metabolomics (SECIM) |
Laboratory | Arthur Edison |
Last Name | Chaevien |
First Name | Clendinen |
Address | R3-226 Academic Research Building, Department of Biochemistry & Molecular Biology, PO Box 100245, Gainesville, FL 32610-0245 |
csclendinen@ufl.edu | |
Phone | 352-392-4535 |
Submit Date | 2014-09-25 |
Num Groups | 2 |
Total Subjects | 4 |
Raw Data Available | Yes |
Raw Data File Type(s) | fid |
Uploaded File Size | 3.1 G |
Analysis Type Detail | NMR |
Release Date | 2016-06-18 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000095 |
Project DOI: | doi: 10.21228/M8S88T |
Project Title: | 13C Metabolomics using INADEQUATE |
Project Summary: | Demonstrate a method using high-sensitivity NMR to identify an unknown metabolite from a fraction isolated from an IROA LC-MS experiment. |
Institute: | University of Florida |
Department: | Department of Biochemistry and Molecular Biology and Southeastern Center for Integrated Metabolomics (SECIM) |
Laboratory: | Edison |
Last Name: | Edison |
First Name: | Arthur |
Email: | aedison@ufl.edu |
Phone: | 352-392-4535 |
Subject:
Subject ID: | SU000122 |
Subject Type: | Invertebrate |
Subject Species: | Caenorhabditis elegans |
Taxonomy ID: | 6239 |
Genotype Strain: | Wild Type (N2) |
Gender: | Hermaphrodites |
Species Group: | Invertebrate |
Factors:
Subject type: Invertebrate; Subject species: Caenorhabditis elegans (Factor headings shown in green)
mb_sample_id | local_sample_id | Incubation Temperature |
---|---|---|
SA005669 | Control_2 | 22 C |
SA005670 | Control_3 | 22 C |
SA005671 | Control_4 | 22 C |
SA005672 | Control_1 | 22 C |
SA005673 | HS_4 | 33 C |
SA005674 | HS_2 | 33 C |
SA005675 | HS_3 | 33 C |
SA005676 | HS_1 | 33 C |
Showing results 1 to 8 of 8 |
Collection:
Collection ID: | CO000105 |
Collection Summary: | Supernatant (exometabolome) and worm pellet (endometabolome) were collected from each flask via centrifugation. The supernatant was filtered using a 20 ?m nylon syringe filter and lyophilized. The worm pellets were homogenized using a Biospec Mini-Beadbeater 8 in 80% methanol and dried. |
Sample Type: | Whole worm extract |
Collection Location: | University of Florida |
Storage Conditions: | -80 celsius |
Treatment:
Treatment ID: | TR000123 |
Treatment Summary: | Two generations of wild-type C. elegans (N2) were fed 99% labeled e. coli. Upon reaching the young adult stage, 4 replicates of 1 million worms each were designated as the experimental population and were treated to a 30 minute heat shock by incubating at 33 °C in the absence of food. After 30 minutes of heat shock, the experimental populations were incubated at room temperature (22 °C) for an additional 1.5 hours. In addition 4 additional replicates of 1 million worms each were designated as the control population and was incubated at room temperature (22 °C) 2 hours in the absence of food. |
Sample Preparation:
Sampleprep ID: | SP000118 |
Sampleprep Summary: | Exometabolome samples were resuspended in 50 ul of Dueterium Oxide (D2O) and the Endometabolome were resuspended in 50 ul of Deuterated Methanol (MeOD). |
Processing Method: | Lyophilization |
Extract Storage: | -80 celsius |
Sample Resuspension: | 50 microliters of D2O or MeOD |
Analysis:
Analysis ID: | AN000171 |
Laboratory Name: | Arthur Edison |
Analysis Type: | NMR |
Analysis Comments: | Data was processed in NMRpipe |
Software Version: | VNMRJ |
Operator Name: | Chaevien Clendinen |
Chromatography ID: | CH000117 |
Num Factors: | 2 |
NMR:
NMR ID: | NM000038 |
Analysis ID: | AN000171 |
Instrument Name: | Agilent VNMRS-600 |
Instrument Type: | FT-NMR |
NMR Experiment Type: | 2D-INADEQUATE |
Spectrometer Frequency: | 600 MHz |
NMR Probe: | 1.5 mm HTS probe |
NMR Solvent: | D2O and MeOD |
NMR Tube Size: | 1.5 mm |
Pulse Sequence: | INADEQUATEAD |
Pulse Width: | 15.6 |
Power Level: | 37 |
Receiver Gain: | 60 |
Temperature: | 23 |
Number Of Scans: | 4 |
Dummy Scans: | 32 |
Acquisition Time: | 0.067 |
Relaxation Delay: | 3 sec |
Spectral Width: | 30487.8 Hz |
Num Data Points Acquired: | 4096 |
Real Data Points: | 2048 |
Zero Filling: | 2x |
Apodization: | Lorentz-to-Gaussian |
Baseline Correction Method: | POLY |