Summary of Study ST001326

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 PR000903. The data can be accessed directly via it's Project DOI: 10.21228/M8ZQ3Z 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.

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Study IDST001326
Study TitleUntargeted lipidome changes in Chlamydomonas reinhardtii treated with small molecules containing adamantane structures
Study SummaryA study to investigate the effect of small molecule lipid inducing compounds that leads to hyper accumulation of lipids in N replete cells of Chlamydomonas reinhardtii. These compounds were identified through a high throughput screening designed for that purpose. During that screening, we screened 43,783 compounds and identified 367 primary hits. These 367 hits were further retested using a 8-point dilution series (from 0.25 to 30 uM) and verified the activity of 250 compounds that induce the hyper lipid accumulating phenotype in algae. Once the hit compounds were identified and confirmed, we then performed extensive chemoinformatics analysis to look for common scaffolds and identified several common substructures. We then selected 15 top performing compounds from 5 diverse structural groups and tested biochemical parameters such as growth, lipid accumulating capacity, effect on photosynthetic rates, respiration rates, oxygen consumption rates, analysis of different lipid species to quantify and identify fatty acid species using GC-MS. To understand the global changes in the lipidome, 2 structurally similar compounds were selected and compared with cells grown without compounds as control for untargeted lipidome analysis.
Institute
University of Nebraska-Lincoln
DepartmentDepartment of Biochemistry
Last NameWase
First NameNishikant
AddressDepartment of Biochemistry, 1901 VINE STREET
Emailnishikant.wase@gmail.com
Phone4023109931
Submit Date2020-03-09
Raw Data AvailableYes
Raw Data File Type(s)mzXML
Analysis Type DetailLC-MS
Release Date2020-04-03
Release Version1
Nishikant Wase Nishikant Wase
https://dx.doi.org/10.21228/M8ZQ3Z
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN002208
Analysis type MS
Chromatography type Reversed phase
Chromatography system Agilent 1200 Series HPLC
Column ACE 5 C8-300 (100 x 2.1mm)
MS Type ESI
MS instrument type FT-ICR
MS instrument name Bruker Solarix FT-ICR-MS
Ion Mode POSITIVE
Units intesity
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