Summary of Study ST004388

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 PR002781. The data can be accessed directly via it's Project DOI: 10.21228/M8626Q This work is supported by NIH grant, U2C- DK119886.

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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 IDST004388
Study TitleUntargeted metabolomics to unravel the adaptations of the desert shrub Haloxylon salicornicum
Study SummaryThis study investigated the metabolic adjustments of the desert shrub Haloxylon salicornicum during drought and subsequent recovery after rewatering. An untargeted metabolomics approach using Orbitrap GC–MS was employed to profile the primary metabolites accumulated in shoots and roots in response to 15 days of water withholding followed by 15 days of rewatering. Six-month-old H. salicornicum seedlings grown in pots were divided into two groups: control plants irrigated every other day and drought-stressed plants subjected to water withholding for 15 days. Shoots and roots were sampled from four seedlings in each group, while the remaining seedlings from both control and drought-stressed treatments were rewatered for an additional 15 days for recovery assessment. Comparisons of the metabolic profiles were made between control and drought-stressed seedlings after 15 days of treatment, and between rewatered and control seedlings after 15 days of recovery. Drought exposure induced the accumulation of 25 metabolites in shoots and 24 in roots, among which eight compounds, γ-aminobutyrate, glutathione, cystine, valine, leucine, ribitol, succinate, and N-acetylputrescine were consistently upregulated in both organs. These shared metabolites collectively represent an integrated drought-response strategy involving stress signal transduction, antioxidant defense, and osmotic adjustment to sustain cellular homeostasis under drought. Shoots specifically accumulated metabolites such as oleic acid and galacturonate, which are implicated in cuticle biosynthesis and cell wall remodeling, as well as amino acids and tricarboxylic acids supporting energy supply and C-N balance under drought. In contrast, roots exhibited elevated levels of sugar alcohols contributing to osmotic adjustment, along with increased accumulation of UDP-glucuronate, which reinforces cell wall rigidity. Following rehydration, seedlings did not fully return to the pre-stress metabolic state but displayed partial recovery characterized by renewed carbohydrate metabolism and sustained levels of stress-related metabolites.
Institute
Sultan Moulay Slimane University
Last NameEzzine
First NameHasna
AddressBzou, Azilal, Morocco
Emailhasnaezzine1@gmail.com
Phone+212648297165
Submit Date2025-11-13
Raw Data AvailableYes
Raw Data File Type(s)mzML, raw(Thermo)
Analysis Type DetailGC-MS
Release Date2025-12-15
Release Version1
Hasna Ezzine Hasna Ezzine
https://dx.doi.org/10.21228/M8626Q
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR002781
Project DOI:doi: 10.21228/M8626Q
Project Title:Desert plant metabolomics
Project Type:Untargeted metabolomics
Project Summary:This project aims to identify the primary metabolites involved in desert plant adaptations to desert harshness
Institute:Sultan Moulay Slimane University
Department:Biology & Geology department
Laboratory:Polyvalent team in Research & development
Last Name:Ezzine
First Name:Hasna
Address:Bzou, Azilal, Morocco
Email:hasnaezzine1@gmail.com
Phone:+212648297165

Subject:

Subject ID:SU004547
Subject Type:Plant
Subject Species:Haloxylon salicornicum
Taxonomy ID:454511

Factors:

Subject type: Plant; Subject species: Haloxylon salicornicum (Factor headings shown in green)

mb_sample_id local_sample_id Sample source Treatment
SA520983CR4Root Control 15D
SA520984CR1Root Control 15D
SA520985CR2Root Control 15D
SA520986CR3Root Control 15D
SA520987CMR3Root Control 1M
SA520988CMR4Root Control 1M
SA520989CMR2Root Control 1M
SA520990CMR1Root Control 1M
SA520991DR1Root Drought
SA520992DR2Root Drought
SA520993DR3Root Drought
SA520994DR4Root Drought
SA520995RR1Root Recovery
SA520996RR3Root Recovery
SA520997RR4Root Recovery
SA520998RR2Root Recovery
SA520999CS1Shoot Control 15D
SA521000CS4Shoot Control 15D
SA521001CS2Shoot Control 15D
SA521002CS3Shoot Control 15D
SA521003CMS3Shoot Control 1M
SA521004CMS4Shoot Control 1M
SA521005CMS2Shoot Control 1M
SA521006CMS1Shoot Control 1M
SA521007DS4Shoot Drought
SA521008DS3Shoot Drought
SA521009DS2Shoot Drought
SA521010DS1Shoot Drought
SA521011RS1Shoot Recovery
SA521012RS2Shoot Recovery
SA521013RS3Shoot Recovery
SA521014RS4Shoot Recovery
Showing results 1 to 32 of 32

Collection:

Collection ID:CO004540
Collection Summary:Shoot and root tissues were immediately frozen in liquid nitrogen during sampling befoe being freeze-dried and powdered
Sample Type:plant tissue

Treatment:

Treatment ID:TR004556
Treatment Summary:Haloxylon salicornicum seedlings were grown in pots containing 75% of sand and 25% of peat moss. The seedlings were divided into two groups: control plants irrigated every other day and drought-stressed plants subjected to water withholding for 15 days. Shoots and roots were sampled from four seedlings in each group, while the remaining seedlings from both control and drought-stressed treatments were rewatered for an additional 15 days for recovery assessment.

Sample Preparation:

Sampleprep ID:SP004553
Sampleprep Summary:Approximately 30 mg of the powdered tissue was transferred to 2 mL Eppendorf tubes containing a few 0.5 mm glass beads, and 1 mL of M1 (methyl-tert-bethyl ether/ methanol; 3:1) was added. The mixture was then homogenized in the Bead Blaster 24R (Benchmark Scientific) by subjecting it to 3 cycles of shaking at 4 °C for 1.5 minutes, followed by an immediate sonication at 0 °C for 20 min. A 650 µL of the phase separation solution M2 (water/methanol; 3:1) was added, and the homogenate was immediately vortexed for 1 min and then centrifuged at 20,000 rpm for 2 min.

Combined analysis:

Analysis ID AN007331
Chromatography ID CH005563
MS ID MS007025
Analysis type MS
Chromatography type GC
Chromatography system Thermo Scientific Exploris GC 240
Column Thermo Scientific Trace GOLD TG-5SilMS (30 m × 0.25 mm, 0.25 um)
MS Type EI
MS instrument type Orbitrap
MS instrument name Thermo Orbitrap Exploris 240
Ion Mode POSITIVE
Units peak intensity

Chromatography:

Chromatography ID:CH005563
Instrument Name:Thermo Scientific Exploris GC 240
Column Name:Thermo Scientific Trace GOLD TG-5SilMS (30 m × 0.25 mm, 0.25 um)
Column Temperature:250 °C
Flow Gradient:-
Flow Rate:1.2 mL/min
Solvent A:-
Solvent B:-
Chromatography Type:GC

MS:

MS ID:MS007025
Analysis ID:AN007331
Instrument Name:Thermo Orbitrap Exploris 240
Instrument Type:Orbitrap
MS Type:EI
MS Comments:The mass spectrometer was operated in positive electron ion mode within a mass-to-charge (m/z) scan range of 35-700, at a temperature of 300 °C, with an orbitrap resolution of 60,000 (FWHM, measured at m/z 200)
Ion Mode:POSITIVE
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