Summary of Study ST001103

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 PR000738. The data can be accessed directly via it's Project DOI: 10.21228/M88X0P This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

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Study IDST001103
Study TitleContinuous in vivo metabolism by NMR
Study SummaryMetabolomics relies on analytical methods to provide holistic information about metabolites, their distributions across samples, and their underlying dynamic properties. The latter is gaining increasing attention due to advances in modeling and new analytical methods that provide dense time-series data. We extended high-resolution-magic angle spinning (HR-MAS) NMR—an established technique to measure metabolites from tissues and live organisms—into a flexible, untargeted, and continuous recording of in vivo metabolism. We call this technique “continuous in vivo metabolism by NMR” (CIVM-NMR). We used isotope-edited CIVM-NMR to reproduce a recent amino acid flux result in chronic lymphoid leukemia cells. We then collected untargeted CIVM-NMR datasets for Neurospora crassa, a classic multicellular model of biochemistry, genetics, and metabolism. CIVM-NMR requires virtually no sample preparation and allows for continuous collection of data over hours to days at ~4-min temporal resolution with little noise. CIVM-NMR provided real-time measurements that unambiguously reproduced the direction of flux of branched-chain amino acid accumulation in leukemia cells. It also revealed the dynamics of central carbon metabolism, amino acid metabolism, energy storage molecules, and lipid and cell wall precursors in N. crassa. CIVM-NMR is simple and readily adapted to different types of cells and microorganisms, making it ideally suited to experimentally complement kinetic models of metabolism for diverse biological systems.
Institute
University of Georgia
Last NameJudge
First NameMichael
Address315 Riverbend Rd., Edison Lab, Athens, GA, 30605, USA
Emailjudgemt@uga.edu
Phone7046771037
Submit Date2018-11-27
Num Groups2
Total Subjects6
Raw Data AvailableYes
Raw Data File Type(s)fid
Analysis Type DetailNMR
Release Date2019-07-17
Release Version1
Michael Judge Michael Judge
https://dx.doi.org/10.21228/M88X0P
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000738
Project DOI:doi: 10.21228/M88X0P
Project Title:Continuous in vivo metabolism by NMR
Project Summary:Metabolomics relies on analytical methods to provide holistic information about metabolites, their distributions across samples, and their underlying dynamic properties. The latter is gaining increasing attention due to advances in modeling and new analytical methods that provide dense time-series data. We extended high-resolution-magic angle spinning (HR-MAS) NMR—an established technique to measure metabolites from tissues and live organisms—into a flexible, untargeted, and continuous recording of in vivo metabolism. We call this technique “continuous in vivo metabolism by NMR” (CIVM-NMR). We used isotope-edited CIVM-NMR to reproduce a recent amino acid flux result in chronic lymphoid leukemia cells. We then collected untargeted CIVM-NMR datasets for Neurospora crassa, a classic multicellular model of biochemistry, genetics, and metabolism. CIVM-NMR requires virtually no sample preparation and allows for continuous collection of data over hours to days at ~4-min temporal resolution with little noise. CIVM-NMR provided real-time measurements that unambiguously reproduced the direction of flux of branched-chain amino acid accumulation in leukemia cells. It also revealed the dynamics of central carbon metabolism, amino acid metabolism, energy storage molecules, and lipid and cell wall precursors in N. crassa. CIVM-NMR is simple and readily adapted to different types of cells and microorganisms, making it ideally suited to experimentally complement kinetic models of metabolism for diverse biological systems.
Institute:University of Georgia
Department:Genetics; Biochemistry and Molecular Biology
Laboratory:Arthur S. Edison
Last Name:Judge
First Name:Michael
Address:315 Riverbend Rd., Edison Lab, Athens, GA, 30605, USA
Email:judgemt@uga.edu
Phone:7046771037
Funding Source:NSF 1713746; NSF ERC 1648035 (CMaT); Georgia Research Alliance
Contributors:Michael T. Judge, Yue Wu, Fariba Tayyari, John Glushka, Ayuna Hattori, Takahiro Ito, Jonathan Arnold, Arthur S. Edison

Subject:

Subject ID:SU001147
Subject Type:Fungi
Subject Species:Neurospora crassa
Taxonomy ID:5141
Genotype Strain:bd1859

Factors:

Subject type: Fungi; Subject species: Neurospora crassa (Factor headings shown in green)

mb_sample_id local_sample_id Condition
SA075125aer_4aerobic
SA075126aer_6aerobic
SA075127aer_5aerobic
SA075128anaer_12anaerobic
SA075129anaer_10anaerobic
SA075130anaer_11anaerobic
Showing results 1 to 6 of 6

Collection:

Collection ID:CO001141
Collection Summary:Mycelia were added with fresh media to a 4mm zirconia HR-MAS rotor with a sealed cap (anaerobic) or a cap with a drilled hole (aerobic). Sample was spun at 6KHz, and spectra were collected continuously over the course of 12h (4.2 min resolution).
Sample Type:mycelia in media

Treatment:

Treatment ID:TR001161
Treatment Summary:Time series were taken on aerobic and anaerobic cultures

Sample Preparation:

Sampleprep ID:SP001154
Sampleprep Summary:Mycelia were added to the HR-MAS rotor with fresh media containing 1mM DSS as a reference.

Analysis:

Analysis ID:AN001793
Analysis Type:NMR
Num Factors:2

NMR:

NMR ID:NM000136
Analysis ID:AN001793
Instrument Name:Bruker NEO
Instrument Type:FT-NMR
NMR Experiment Type:1D 1H
Spectrometer Frequency:600 MHz
NMR Probe:4mm CMP HR-MAS Probe
NMR Solvent:Vogels Media containing 5% D2O and 1mM DSS
NMR Tube Size:5mm
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