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Sample GSM256870 Query DataSets for GSM256870
Status Public on Jul 15, 2008
Title Ecoli_untreated_-5min_rep3
Sample type RNA
 
Source name Untreated E. coli -5 minute
Organism Escherichia coli K-12
Characteristics MG1655
Treatment protocol Antibiotics were added to final concentration of 10 ug/ml cefsulodin and 0.03 ug/ml mecillinam when the culture reached an OD of approximately 0.2. In the case of the combination treatment the same concentrations were used but the antibiotics were measured and mixed prior to addition.
Growth protocol Cultures of MG1655 were grown overnight at 37°C for 14-16 hours Cultures of SEA113 (MG1655) were grown in LB at 37°C overnight (14-18 hrs) with rotation. The overnight cultures were diluted in fresh media to an OD600 of 0.02 and grown at 37°C with shaking in a gyrotary water bath until an OD600 of 0.2, at which point antibiotics were added.
Extracted molecule total RNA
Extraction protocol Samples were collected from both the treated and untreated cultures 5 minutes before treatment as well as 5, 20 and 40 minutes after treatment. The 40 minute time point was immediately before cell growth slowed due to antibiotic treatment. 10 ml of culture was added to an ice-cold 5% phenol/ethanol solution to stop further transcription. RNA was extracted using the hot phenol method of extraction.
Label biotin
Label protocol Biotinylated cDNA were prepared according to the standard Affymetrix protocol from 20 ug total RNA (Expression Analysis Technical Manual).
 
Hybridization protocol Labeled cDNA was hybridized according to the Affymetrix manual for E. coli Antisense chips and were washed and stained in the GeneChip Fluids Station 400
Scan protocol Chips were scanned with the GCS3000 scanner
Description Gene expression data from untreated E. coli cells
Data processing The data were analyzed with the robust multichip averaging (RMA) program in the Simpleaffy package for the Bioconductor statistics environment. Genes with significant changes in gene expression were identified using the significance analysis of microarrays (SAM) program using two-way paired comparison with a false discovery rate of 0.958 % for cef/mec.
 
Submission date Jan 12, 2008
Last update date Jan 12, 2008
Contact name Mary Elizabeth Laubacher
E-mail(s) mel23@psu.edu
Phone 814-863-1075
Organization name Pennsylvania State University
Department Biochemistry Microbiology and Molecular Biology
Lab Ades
Street address 317 S Frear
City University Park
State/province PA
ZIP/Postal code 16802
Country USA
 
Platform ID GPL199
Series (2)
GSE10158 Expression of Escherichia coli treated with cefsulodin and mecillinam, alone and in combination
GSE10160 Expression of Escherichia coli treated with cefsulodin and mecillinam

Data table header descriptions
ID_REF
VALUE RMA Signal

Data table
ID_REF VALUE
aas_b2836_at 8.867800514
aat_b0885_at 8.659061828
abc_b0199_at 9.763985179
abrB_b0715_at 7.877635646
accA_b0185_at 10.49621854
accB_b3255_at 13.25447845
accC_b3256_at 11.73609181
accD_b2316_at 11.03755179
aceA_b4015_at 7.602925373
aceB_b4014_at 8.705040693
aceE_b0114_at 13.80748373
aceF_b0115_at 13.46937276
aceK_b4016_at 7.848701348
ackA_b2296_at 13.78673361
acnA_b1276_at 8.227006654
acnB_b0118_at 9.143211954
acpD_b1412_at 8.146484593
acpP_b1094_at 13.89772091
acpS_b2563_at 9.276336605
acrA_b0463_at 11.82284342

Total number of rows: 7312

Table truncated, full table size 228 Kbytes.




Supplementary file Size Download File type/resource
GSM256870.CEL.gz 1.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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