Summary of Study ST001511

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 PR001018. The data can be accessed directly via it's Project DOI: 10.21228/M83T2V This work is supported by NIH grant, U2C- DK119886.

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

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.

Show all samples  |  Perform analysis on untargeted data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST001511
Study TitleSymbiotic bacteria-derived organic acids
Study SummaryMetabolomic profiles of six bacteria and K. oxytoca were compared to identify candidate metabolites that may prevent B. bassiana infection of D. antiqua.
Institute
Qilu University of Technology (Shandong Academy of Sciences)
Last NameZhou
First NameFangyuan
AddressNo. 28789 Jingshidong Road, Jinan, Shandong, 250103, China
Emailfangyuan_zhou@163.com
Phone+8618511761347
Submit Date2020-09-10
Raw Data AvailableYes
Raw Data File Type(s)wiff
Analysis Type DetailLC-MS
Release Date2022-01-02
Release Version1
Fangyuan Zhou Fangyuan Zhou
https://dx.doi.org/10.21228/M83T2V
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Combined analysis:

Analysis ID AN002504 AN002505
Analysis type MS MS
Chromatography type HILIC HILIC
Chromatography system Unspecified Unspecified
Column Waters Acquity BEH Amide (150 x 2.1mm,1.7um) Waters Acquity BEH Amide (150 x 2.1mm,1.7um)
MS Type EI EI
MS instrument type QTOF QTOF
MS instrument name ABI Sciex 5600+ TripleTOF ABI Sciex 5600+ TripleTOF
Ion Mode POSITIVE NEGATIVE
Units peak area peak area

Chromatography:

Chromatography ID:CH001831
Chromatography Summary:All samples from the nine groups were analyzed by a LC-MS system. First, all chromatographic separations were performed using an ultra-performance liquid chromatography (UPLC) system (SCIEX, UK) equipped with an ACQUITY UPLC BEH Amide column (100 mm×2.1 mm, 1.7 µm, Waters, UK) for the reversed-phase separation. The column oven was maintained at 35 °C. The flow rate was 0.4 mL/min and the mobile phase consisted of solvent A (25 mM ammonium acetate) and solvent B (isopropanol: acetonitrile =9:1 + 0.1% formic acid). Gradient elution conditions were set as follows: 0-0.5 min, 95% B; 0.5-9.5 min, 95% to 65% B; 9.5-10.5 min, 65%-40% B; 10.5-12 min, 40% B; 12-12.2 min, 40%-95% B; and 12.2-15 min, 95% B. The injection volume for each sample was 4 µL.
Instrument Name:Unspecified
Column Name:Waters Acquity BEH Amide (150 x 2.1mm,1.7um)
Column Temperature:35
Flow Gradient:0-0.5 min, 95% B; 0.5-9.5 min, 95% to 65% B; 9.5-10.5 min, 65%-40% B; 10.5-12 min, 40% B; 12-12.2 min, 40%-95% B; and 12.2-15 min, 95% B.
Flow Rate:0.4 mL/min
Solvent A:100% water; 25 mM ammonium acetate
Solvent B:90% isopropanol/10% acetonitrile; 0.1% formic acid
Chromatography Type:HILIC
  logo