Summary of Study ST000569

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 PR000417. The data can be accessed directly via it's Project DOI: 10.21228/M8531V This work is supported by NIH grant, U2C- DK119886.

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

Study ID	ST000569
Study Title	Effect of minimal and complex media on the metabolite profiles
Study Summary	Media dependent intracellular metabolite changes of microorganisms
Institute	Graduate school of Korea University
Last Name	Kim
First Name	Jungyeon
Address	145, Anam-ro, Seongbuk-gu, Seoul, Seoul, 02841, Korea, South
Email	kim131812@korea.ac.kr
Phone	821082248015
Submit Date	2017-03-07
Study Comments	Each class means,Intracellular metabolites of E.coli cultivated in M9 Intracellular metabolites of E.coli cultivated in LB Intracellular metabolites of S.cerevisiae cultivated in YNB Intracellular metabolites of S.cerevisiae cultivated in YPD.
Raw Data Available	Yes
Raw Data File Type(s)	peg
Analysis Type Detail	GC-MS
Release Date	2017-07-10
Release Version	1

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Treatment:

Treatment ID:	TR000605
Treatment Summary:	E. coli MG1655 was cultivated in a 100-ml working volume in 250 ml flasks at 37 °C, with shaking at 200 rpm. The culture media for E. coli MG1655 were minimal M9 medium (Difco Laboratories, Detroit, MI) and complex Luria broth (Difco Laboratories). S. cerevisiae BY4741 was cultivated in a 100-ml working volume in 250 ml flasks at 30 °C, with shaking at 200 rpm. The culture media were a minimal medium of the yeast nitrogen base broth (Difco Laboratories) and a complex medium of YP broth (Difco Laboratories). All media contained 2% (w/v) glucose as a sole carbon source.

Treatment ID:

TR000605

Treatment Summary:

E. coli MG1655 was cultivated in a 100-ml working volume in 250 ml flasks at 37 °C, with shaking at 200 rpm. The culture media for E. coli MG1655 were minimal M9 medium (Difco Laboratories, Detroit, MI) and complex Luria broth (Difco Laboratories). S. cerevisiae BY4741 was cultivated in a 100-ml working volume in 250 ml flasks at 30 °C, with shaking at 200 rpm. The culture media were a minimal medium of the yeast nitrogen base broth (Difco Laboratories) and a complex medium of YP broth (Difco Laboratories). All media contained 2% (w/v) glucose as a sole carbon source.