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Sample GSM1608470 Query DataSets for GSM1608470
Status Public on Jul 28, 2015
Title ST rpoN_compl biol1 over ST rpoN biol2
Sample type RNA
 
Channel 1
Source name rpoN-comp complemented mutant cells grown statically until OD(600nm)=0.2
Organism Bacillus cereus ATCC 14579
Characteristics strain derivative: ΔrpoN-comp
Treatment protocol Cells were harvested at above mentioned timepoints (see overall design) without any additional treatment.
Growth protocol Liquid cultures of B. cereus ATCC14579 WT, ΔrpoN and ΔrpoN-comp strains were grown in BHI with aeration (200rpm) and statically in Erlenmeyer flasks at 30°C.
Extracted molecule total RNA
Extraction protocol Cultures were spinned down, resuspended in 1 ml TRI reagent (Ambion) and snap frozen in liquid nitrogen. RNA was extracted according to the RNAwiz (Ambion) protocol using Chloroform/isopropanol extraction. Residual DNA was enzymatically removed using the TURBO DNA-free (Ambion) kit following the instructions of the manufacturer.
Label cy5
Label protocol Cy3 and Cy5 labeling of the cDNA was performed with CyScribe Post-Labeling kit (GE Healthcare)
 
Channel 2
Source name rpoN deletion mutant cells grown statically until OD(600nm)=0.2
Organism Bacillus cereus ATCC 14579
Characteristics strain derivative: ΔrpoN
Treatment protocol Cells were harvested at above mentioned timepoints (see overall design) without any additional treatment.
Growth protocol Liquid cultures of B. cereus ATCC14579 WT, ΔrpoN and ΔrpoN-comp strains were grown in BHI with aeration (200rpm) and statically in Erlenmeyer flasks at 30°C.
Extracted molecule total RNA
Extraction protocol Cultures were spinned down, resuspended in 1 ml TRI reagent (Ambion) and snap frozen in liquid nitrogen. RNA was extracted according to the RNAwiz (Ambion) protocol using Chloroform/isopropanol extraction. Residual DNA was enzymatically removed using the TURBO DNA-free (Ambion) kit following the instructions of the manufacturer.
Label cy3
Label protocol Cy3 and Cy5 labeling of the cDNA was performed with CyScribe Post-Labeling kit (GE Healthcare)
 
 
Hybridization protocol Hybridization was performed as described in Mols et al., 2013.
Scan protocol Slides were scanned with Agilent G2505C scanner
Description Expression profiles of the rpoN deletion mutant (ΔrpoN) and the complemented strain (ΔrpoN-comp) were compared to the parental strain (WT) at static growth
Data processing Data were normalized using Lowess normalisation as available in MicroPrep and corrected for inter-slide differences. Median intensity of the different probes per gene and biological replicate was selected as the gene expression intensity.
 
Submission date Feb 12, 2015
Last update date Jul 28, 2015
Contact name Jos Boekhorst
E-mail(s) [email protected]
Organization name NIZO food research
Street address Kernhemseweg 2
City Ede
ZIP/Postal code 6718 ZB
Country Netherlands
 
Platform ID GPL19768
Series (1)
GSE65894 Transcriptome comparison between Bacillus cereus ATCC 14579 wildtype (WT), RpoN (Sigma 54) deletion mutant and the complemented strain.

Data table header descriptions
ID_REF
VALUE log2 of normalized ratio (Cy5/Cy3)
PRE_VALUE Normalized ratio (Cy5/Cy3)

Data table
ID_REF VALUE PRE_VALUE
BC0001 1.2852 2.437240216
BC0002 1.5726 2.974391185
BC0003 -0.1831 0.880786573
BC0004 0.0082 1.005732842
BC0005 0.0272 1.019004643
BC0006 0.7471 1.678415352
BC0012 -2.2998 0.203094769
BC0013 -0.0535 0.96361554
BC0014 1.7942 3.468281601
BC0015 0.3196 1.247951268
BC0016 0.5017 1.41589829
BC0017 1.1592 2.233259944
BC0019 0.2190 1.163894384
BC0020 3.0424 8.238533693
BC0021 2.2531 4.766926928
BC0022 -0.7294 0.60314548
BC0023 -0.1985 0.871456999
BC0024 -1.8456 0.278241761
BC0025 -0.7108 0.610995604
BC0026 -0.5331 0.691078038

Total number of rows: 5270

Table truncated, full table size 134 Kbytes.




Supplementary file Size Download File type/resource
GSM1608470_US22502548_251734310075_S01_GE2_107_Sep09_2_2.txt.gz 3.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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