Summary of Study ST001852

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 PR001168. The data can be accessed directly via it's Project DOI: 10.21228/M8QT2F 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 IDST001852
Study TitleScreening of unique bile acid metabolizing bacteria
Study SummaryWe incubated individual bacterial strains at pH 7 or pH 9 with either CDCA, LCA, or 3-oxo-Δ4-LCA as starting substrates. Culture supernatants were collected after 48 hours and 14 bile acids were measured by targeted metabolomics.
Institute
Keio University School of Medicine
DepartmentDept of Microbiology and Immunology
Last NameKoji
First NameAtarashi
Address35 Shinanomachi, Shinjuku-ku, Tokyo, JAPAN
Emailkojiatarashi@keio.jp
Phone0353633769
Submit Date2021-06-24
Raw Data AvailableYes
Raw Data File Type(s)lcd
Analysis Type DetailLC-MS
Release Date2021-07-07
Release Version1
Atarashi Koji Atarashi Koji
https://dx.doi.org/10.21228/M8QT2F
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN003000
Analysis type MS
Chromatography type Reversed phase
Chromatography system Shimadzu CBM20A
Column InertSustain C18
MS Type ESI
MS instrument type Triple quadrupole
MS instrument name Shimadzu LCMS-8040
Ion Mode UNSPECIFIED
Units uM

Chromatography:

Chromatography ID:CH002225
Chromatography Summary:2 μL of the solution was injected to LC/ESI-MS/MS (LC-MS8040 tandem mass spectrometer, equipped with an ESI probe and Nexera X2 ultra-high-pressure liquid chromatography system; Shimadzu). A separation column, InertSustain C18 (150 mm × 2.1 mm ID, 2 μm particle size; GL Sciences Inc.), was utilized at 40 °C. Mixture A (10 mM ammonium acetate, 0.01% formic acid, and 20% acetonitrile) and mixture B (30% acetonitrile and 70% methanol) were used as the eluent, and the separation was carried out by linear gradient elution at a flow rate of 0.2 mL/min. The mobile phase composition was gradually changed as follows: Mixture A:B (80:20, v/v) for 0.1 min, (48:52, v/v) for 0.1-1 min, (30:70, v/v) for 1-27 min, (0:100, v/v) for 27-27.1 min, (0:100, v/v) for 27.1-33 min, (80:20, v/v) for 33-33.1 min, and (80:20 v/v) for 33.1-83 min. The total run time was 38 min.
Instrument Name:Shimadzu CBM20A
Column Name:InertSustain C18
Column Temperature:40
Flow Gradient:The mobile phase composition was gradually changed as follows: Mixture A:B (80:20, v/v) for 0.1 min, (48:52, v/v) for 0.1-1 min, (30:70, v/v) for 1-27 min, (0:100, v/v) for 27-27.1 min, (0:100, v/v) for 27.1-33 min, (80:20, v/v) for 33-33.1 min, and (80:20 v/v) for 33.1-83 min. The total run time was 38 min.
Flow Rate:0.2ml/min
Solvent A:20% acetonitrile/80% water; 0.01% formic acid; 10mM ammonium acetate
Solvent B:30% acetonitrile/70% methanol
Chromatography Type:Reversed phase
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