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Sample GSM256896 Query DataSets for GSM256896
Status Public on Jul 15, 2008
Title Ecoli_treated_mecillinam0.03_40min_rep2
Sample type RNA
 
Source name Treated E. coli 0.03 ug/ml mecillinam 40 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 E. coli cells treated with 0.03 ug/ml mecillinam
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 8.831442034
aat_b0885_at 8.715243471
abc_b0199_at 8.513813473
abrB_b0715_at 7.722063424
accA_b0185_at 10.3117613
accB_b3255_at 12.64757553
accC_b3256_at 10.89368995
accD_b2316_at 11.27763439
aceA_b4015_at 9.682173193
aceB_b4014_at 10.06052593
aceE_b0114_at 11.5713
aceF_b0115_at 11.18808307
aceK_b4016_at 7.996197929
ackA_b2296_at 11.50959834
acnA_b1276_at 8.316307403
acnB_b0118_at 9.919331827
acpD_b1412_at 8.467626211
acpP_b1094_at 13.76798249
acpS_b2563_at 9.539607662
acrA_b0463_at 10.92588875

Total number of rows: 7312

Table truncated, full table size 228 Kbytes.




Supplementary file Size Download File type/resource
GSM256896.CEL.gz 1.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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