Summary of Study ST000001

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 PR000001. The data can be accessed directly via it's Project DOI: 10.21228/M8159B This work is supported by NIH grant, U2C- DK119886.

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Study IDST000001
Study TitleFatb Induction Experiment (FatBIE)
Study TypeGenotype treatment
Study SummaryThis experiment tests the consequence of a mutation at the FatB gene (At1g08510) in the wound-response of Arabidopsis. The FatB mutant allele (fatb KD J. Ohlrogge (Plant Cell 2003, Vol 15, 1020-1033)) was obtained from Dr. Katayonn Dehesh, University of California, Davis, Davis, CA. This allele is in the Ws background.The standardized growth conditions are as follows: 1. Seeds (between 14 and 16) are sown on media in 100 x 100 x 15mm square Falcon Petri Dishes (Fisher Scientific, catalogue #08-757-11A). Seeds were arranged on the plates in a single horizontal line at the 1-cm mark from the top of the plate.2. Each plate contains between 20 and 25-ml of sterile MS media containing 0.1% (w/v) sucrose.3. Prior to sowing, seeds were sterilized by treating for 1 minute at room temperature with a 300-l solution of 50% (v/v) ethanol, this solution was removed and replaced with a 300-l solution consisting of 1% (v/v) Tween 20 (Fischer BioReagents, catalogue #BP33750), and 50% (v/v) bleach solution (Clorox), and incubated at room temperature for 10-minutes. The seeds were then washed with three changes of 0.3-ml of sterile water.
Institute
University of California, Davis
DepartmentDavis Genome Center
LaboratoryFiehn
Last NameKind
First NameTobias
Address451 E. Health Sci. Drive, Davis, CA 95616, USA
Emailtkind@ucdavis.edu
Submit Date2013-01-15
Num Groups4
Total Subjects24
Raw Data AvailableNo
Analysis Type DetailGC-MS
Release Date2013-02-14
Release Version1
Tobias Kind Tobias Kind
https://dx.doi.org/10.21228/M8159B
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Treatment:

Treatment ID:TR000001
Treatment:Abiotic
Treatment Route:Wounded
Treatment Dose:Ten punches
Treatment Doseduration:3 min wounding period; 2 h response perioid before harvest
Plant Growth Support:Fourteen to sixteen seeds were sown on 2025 ml of sterile Murashige and Skoog basal salt mixture (MS medium) containing 0.1% w/v sucrose and 1 liquid vitamin solution (Sigma, http://www.sigmaaldrich.com/) containing 15 g l)1 bacto agar (BD) in 100 100 15 mm square Falcon Petri dishes (Thermo Fisher Scientific; http:// www.thermofisher.com). Seeds were arranged on the plates in a single horizontal line 1 cm from the top of the plate. Prior to sowing, seeds were sterilized by treating for 1 min at room temperature with 300 ll of 50% v/v ethanol; this solution was then removed and replaced by 300 ll of a solution consisting of 1% v/v Tween-20 (Thermo Fisher Scientific) and 50% v/v bleach (Clorox; http://www.clorox. com), and incubated at room temperature for 10 min. The seeds were then washed with three changes of 0.3 ml of sterile water. After sowing the seeds, the plates were wrapped using micropore tape (3 M Health Care; http://www.3m.com), and then stored horizontally for 4 days at 4 C in the dark. On the 5th day, plates were moved to the growth room, and held in a vertical position in Plexiglass holders for 12 days.
Plant Growth Location:Controlled-environment facility at Iowa State University, Nikolau laboratory.
Plant Plot Design:Each genotype and replicate were grown on individual plates and placed randomly in the Plexiglass holders.
Plant Light Period:24 h day at 82 micromol/m**2 s (light source Sylvania; http://www.sylvania.com), F34CW/SS/ECO/RP)
Plant Humidity:Day 100%, night 100%
Plant Temp:Day 24 C, night 24 C
Plant Watering Regime:No further watering, plates remained closed
Plant Nutritional Regime:MS medium without further fertilizers
Plant Estab Date:2006-09-25
Plant Harvest Date:2006-10-11
Plant Growth Stage:Boyes 1.11.4
Plant Metab Quench Method:Immersion in liquid nitrogen within 1 min after harvest
Plant Harvest Method:Petri plates were opened and the aerial portions of the plants were cut
Plant Storage:-70 C for 1 day, then shipping on dry ice and storage at -80 C for 2 weeks
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