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Sample GSM1419894 Query DataSets for GSM1419894
Status Public on Jul 18, 2014
Title GLBRCE1_SynH_LT_Stat1_rep327_1
Sample type RNA
 
Source name GLBRCE1, SynH_LT, Stat1
Organism Escherichia coli
Characteristics strain: GLBRCE1
medium: SynH_LT
growth phase: Stat1
biological replicate: 327
technical replicate: 1
Treatment protocol Cells (10 ml) for transcriptomic analysis were collected into tubes containing 1.25 ml ice-cold 5% (vol/vol) unbuffered phenol in ethanol (EP) and pelleted by centrifugation (10,000 g, 4°C, 3 min). To remove residual traces of hydrolysate, cell pellets were twice resuspended in ice-cold GMM plus 0.125 volume of EP, repelleted, then flash frozen in dry ice-ethanol, and stored at -80°C.
Growth protocol Fermentations were carried out in 3 L bioreactors (Applikon Biotechnology) containing 2.45 L of ACSH or SynH media, and cultures were diluted into ACSH or SynH with initial OD at 0.2, grown anaerobically overnight, and then inoculated into bioreactors to a starting OD600 of 0.2
Extracted molecule total RNA
Extraction protocol RNA was obtained from cells pellets by lysozyme treatment and phenol-chloroform extraction, analyzed by agarose gel electrophoresis to confirm integrity, quantified using a Nanodrop spectrophotometer (Thermo Scientific), and stored at -80°C
Label Cy3
Label protocol cDNA labeling protocol was conducted according to the manufacturer’s instructions (Roche NimbleGen)
 
Hybridization protocol hybridization protocol was conducted according to the manufacturer’s instructions (Roche NimbleGen)
Scan protocol Hybridized arrays were scanned with a NimbleGen MS 200 microarray scanner, and the probe signal intensities were determined using NimbleScan v 2.6 (Roche NimbleGen).
Description Exp327_V1_T4
Data processing Probe signal intensities were preprocessed using robust multichip averaging (RMA) in the program ArrayStar (DNASTAR), and the resulting gene expression signals were quantile-normalized across all samples using the normalize.quantiles function in the Bioconductor package for R.
 
Submission date Jun 25, 2014
Last update date Jul 18, 2014
Contact name Robert C Landick
E-mail(s) landick@bact.wisc.edu
Phone (608) 265-8475
Organization name University of Wisconsin - Madison
Department Great Lakes Bioenergy Research Center
Street address 1550 Linden Dr
City Madison
State/province WI
ZIP/Postal code 53706
Country USA
 
Platform ID GPL14649
Series (2)
GSE58806 Aromatic inhibitors derived from ammonia-pretreated lignocellulose hinder bacterial ethanologenesis by activating regulatory circuits controlling inhibitor efflux and detoxification (I)
GSE58927 Aromatic inhibitors derived from ammonia-pretreated lignocellulose hinder bacterial ethanologenesis by activating regulatory circuits controlling inhibitor efflux and detoxification

Data table header descriptions
ID_REF
VALUE RMA-normalized, averaged gene-level signal intensity, quantile-normalized across all samples

Data table
ID_REF VALUE
b0001071000000001 3.109147097
b0002071000000002 47.59780863
b0003071000000003 39.65301579
b0004071000000004 24.37018721
b0005071000000005 1.670927103
b0006071000000006 0.829370404
b0007071000000007 1.069724103
b0008071000000008 11.66118621
b0009071000000009 1.516398579
b0010071000000010 1.116088444
b0011071000000011 0.601656623
b0013071000000012 0.57562904
b0014071000000013 35.20423941
b0015071000000014 11.0997075
b0016071000000015 4.968316268
b0018071000000016 0.491796432
b0019071000000018 2.379981486
b0020071000000019 1.223019647
b0021071000000020 4.504732998
b0022071000000021 5.089238396

Total number of rows: 4254

Table truncated, full table size 124 Kbytes.




Supplementary file Size Download File type/resource
GSM1419894_Exp327_V1_T4_320070A04_renamed.pair.gz 1.0 Mb (ftp)(http) PAIR
Processed data included within Sample table

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