Metabolomics Workbench : NIH Data Repository

MB Sample ID: SA168226

Local Sample ID:	GATp10GLN-3-neg-PRM
Subject ID:	SU001888
Subject Type:	Plant
Subject Species:	Arabidopsis thaliana
Taxonomy ID:	3702
Genotype Strain:	Col-0
Age Or Age Range:	10 day old seedlings
Gender:	Not applicable

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Treatment:

Treatment ID:	TR001901
Treatment Summary:	Wild-type Arabidopsis ecotype Columbia and gat1_2.1 T-DNA insertion lines were used for Gln and Glu treatments. Plants were grown on vertical plates at 22 °C under continuous light (ca. 70 μmol m-2 s-2), as previously described by Ivanov et al. (2012) on a defined nutrient medium containing a final concentration of 10 mM potassium phosphate (pH 6.5), 5 mM KNO3, 2 mM MgSO4, 1 mM CaCl2, 125 μg FeNaEDTA, micronutrients (50 mM H3BO3, 12 mM MnSO4, 1 mM ZnCl2, 1 mM CuSO4 and 0.2 mM Na2MoO4), 1% sucrose and 1% agar [28]. Ten-day old seedlings were transferred to plates containing the same medium without nitrogen as control or 10 mM Gln as sole N source. After 2 h, root tissue was harvested, frozen in liquid N2 and stored at -80 °C until total metabolite extractions was carried out. For growth in Gln and Glu, the same media and growth conditions were used with the exception of 5 mM KNO3 being substituted with either 2 mM Gln or 2 mM Glu and tissue was collected after 10 days.

Treatment ID:

TR001901

Treatment Summary:

Wild-type Arabidopsis ecotype Columbia and gat1_2.1 T-DNA insertion lines were used for Gln and Glu treatments. Plants were grown on vertical plates at 22 °C under continuous light (ca. 70 μmol m-2 s-2), as previously described by Ivanov et al. (2012) on a defined nutrient medium containing a final concentration of 10 mM potassium phosphate (pH 6.5), 5 mM KNO3, 2 mM MgSO4, 1 mM CaCl2, 125 μg FeNaEDTA, micronutrients (50 mM H3BO3, 12 mM MnSO4, 1 mM ZnCl2, 1 mM CuSO4 and 0.2 mM Na2MoO4), 1% sucrose and 1% agar [28]. Ten-day old seedlings were transferred to plates containing the same medium without nitrogen as control or 10 mM Gln as sole N source. After 2 h, root tissue was harvested, frozen in liquid N2 and stored at -80 °C until total metabolite extractions was carried out. For growth in Gln and Glu, the same media and growth conditions were used with the exception of 5 mM KNO3 being substituted with either 2 mM Gln or 2 mM Glu and tissue was collected after 10 days.