Summary of Study ST002215

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 PR001415. The data can be accessed directly via it's Project DOI: 10.21228/M8TD74 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 IDST002215
Study TitleTime course GCMS based untargeted metabolomics in the presence of glucose and glycerol
Study SummaryOur preliminary analysis identifies that glycerol enhanced DHA accumulation in native isolate Aurantiochytrium limacinum. To evaluate temporal changes in the presence of glycerol, time-course metabolite profiling was done in the presence of glycerol and glucose at three different time-points i.e., 0, 48 and 96 h using GC-MS. We identified nearly 40 metabolites, among which metabolites belonging to pentose phosphate pathway, TCA cycle and amino acid metabolism were significantly differentially regulated which suggests its role in glycerol induced DHA accumulation.
Institute
International Centre for Genetic Engineering and Biotechnology
Last NameJutur
First NamePannaga Pavan
AddressOmics of Algae Lab, 2nd Floor, New Building, ICGEB, Aruna Asaf Ali Marg, New Delhi
Emailjppavan@gmail.com
Phone01126741358
Submit Date2022-06-22
Raw Data AvailableYes
Raw Data File Type(s)mzdata.xml
Analysis Type DetailLC-MS
Release Date2023-06-27
Release Version1
Pannaga Pavan Jutur Pannaga Pavan Jutur
https://dx.doi.org/10.21228/M8TD74
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001415
Project DOI:doi: 10.21228/M8TD74
Project Title:Multi-omics analysis of Aurantiochytrium limacinum
Project Type:Time course GCMS based untargeted metabolomics in the presence of glucose and glycerol
Project Summary:To evaluate temporal changes in the presence of glycerol, time-course metabolite profiling was done in the presence of glycerol and glucose at three different time-points i.e., 0, 48 and 96 h using GCMS.
Institute:International Centre for Genetic Engineering and Biotechnology
Department:Omics of Algae
Last Name:Jutur
First Name:Pannaga Pavan
Address:Omics of Algae Group, ICGEB campus, Aruna Asaf Ali Marg, New Delhi, Delhi, 110070, India
Email:jppavan@icgeb.res.in
Phone:26781358

Subject:

Subject ID:SU002301
Subject Type:Other organism
Subject Species:Aurantiochytrium limacinum

Factors:

Subject type: Other organism; Subject species: Aurantiochytrium limacinum (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA211884D0_1Glucose
SA211885D4_Glucose_1Glucose
SA211886D4_Glucose_2Glucose
SA211887D4_Glucose_3Glucose
SA211888D2_Glucose_3Glucose
SA211889D2_Glucose_1Glucose
SA211890D0_2Glucose
SA211891D2_Glucose_2Glucose
SA211892D0_3Glucose
SA211893D4_Glycerol_3Glycerol
SA211894D4_Glycerol_2Glycerol
SA211895D2_Glycerol_2Glycerol
SA211896D2_Glycerol_1Glycerol
SA211897D2_Glycerol_3Glycerol
SA211898D4_Glycerol_1Glycerol
Showing results 1 to 15 of 15

Collection:

Collection ID:CO002294
Collection Summary:Marine thraustochytrid Aurantiochytrium limacinum was a native isolate obtained as a generous gift from ICT-Mumbai, India. It was cultivated in YPD medium with the optimized concentration of 3% (w/v) glucose and glycerol at 20 C for a duration of 96 h.
Sample Type:Cultured cells

Treatment:

Treatment ID:TR002313
Treatment Summary:It was cultivated in YPD medium with the optimized concentration of 3% (w/v) glucose and glycerol at 20 C for a duration of 96 h.
Treatment:Glucose and Glycerol

Sample Preparation:

Sampleprep ID:SP002307
Sampleprep Summary:Quenched cells were resuspended in 1 mL of ice-cold methanol/ethanol/chloroform(2:6:2), followed by sonication of resuspended cells in sonication bath for 15 min. Later, these samples were centrifuged at 10,000×g for 15 min at 4 °C to get rid of cell debris. The supernatant was filtered using a 0.2-µm filter. One hundred microlitres of supernatant was taken and dried under nitrogen stream. The dried leftover was dissolved in 10 µL of freshly prepared methoxyamine hydrochloride solution (40 mg mL−1 in pyridine) and incubated at 30 °C for 90 min with shaking. To the above solution, 90 µL of N-methyl-N-(trimethylsilyl)trifluoroacetamide was added and incubated at 37 °C for 30 min. The samples were centrifuged at 14,000×g for 3 min, and the supernatant was taken for the GC-MS/MS analysis.
Processing Storage Conditions:Described in summary
Sample Derivatization:MSTFA
Sample Spiking:Nonadecanoic acid

Combined analysis:

Analysis ID AN003624
Analysis type MS
Chromatography type GC
Chromatography system Agilent 7890A
Column Agilent DB5-MS (30m x 0.25mm, 0.25um)
MS Type ESI
MS instrument type Triple quadrupole
MS instrument name Agilent 7890A
Ion Mode POSITIVE
Units Area

Chromatography:

Chromatography ID:CH002679
Instrument Name:Agilent 7890A
Column Name:Agilent DB5-MS (30m x 0.25mm, 0.25um)
Chromatography Type:GC

MS:

MS ID:MS003375
Analysis ID:AN003624
Instrument Name:Agilent 7890A
Instrument Type:Triple quadrupole
MS Type:ESI
MS Comments:Mass Hunter
Ion Mode:POSITIVE
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