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Sample GSM1181939 Query DataSets for GSM1181939
Status Public on Jul 09, 2013
Title Control_Tme_30_rep1
Sample type RNA
 
Source name Control
Organism Acetivibrio thermocellus ATCC 27405
Characteristics strain: ATCC 27405
time: 30
treatment: Control
Treatment protocol Clostridium thermocellum was grown in batch fermentation to an OD600 of approximately 0.5 before treatment with either 3.95 g.L-1 ethanol, 3 g.L-1 furfural or the elevated temperature of 68°C. Total RNA was recovered at 10, 30, 60, and 120 min post-treatment for comparison with untreated controls.
Growth protocol Batch fermentations were conducted in approximately 4 L of MTC medium in 7.5 L BioFlo110 biopreactors (New Brunswick Scientific, Edison, NJ) fitted with agitation, pH and temperature probes and controls as described previously (Yang et al., 2008).
Extracted molecule total RNA
Extraction protocol Briefly, samples were harvested by centrifugation and the TRIzol reagent (Invitrogen, Carlsbad, CA) was used to extract total cellular RNA. Each total RNA preparation was treated with RNase-free DNase I (Ambion, Austin, TX) to digest residual chromosomal DNA and subsequently purified with the Qiagen RNeasy Mini kit in accordance with the instructions from the manufacturer. Total cellular RNA was quantified at OD260 and OD280 with a NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE) and the RNA quality was checked with Agilent Bioanalyzer (Agilent, CA). The purified RNA with good quality from each sample was used as the template to generate ds-cDNA using Invitrogen ds-cDNA synthesis kit (Invitrogen, CA).
Label Cy3
Label protocol The labeling, hybridization, and scanning following NimbleGen company's protocols.
 
Hybridization protocol The labeling, hybridization, and scanning following NimbleGen company's protocols.
Scan protocol The labeling, hybridization, and scanning following NimbleGen company's protocols.
Description Control_Tme_30
Data processing Statistical analysis was done with JMP Genomics 4.0 software (SAS Institute, Cary, NC). The data were subsequently normalized using the Loess normalization algorithm within JMP Genomics. An analysis of variance (ANOVA) was performed to determine differential expression levels between conditions and time points using the FDR testing method (p < 0.05).
 
Submission date Jul 08, 2013
Last update date Jul 09, 2013
Contact name Charlotte Wilson
Organization name ORNL
Department Biosciences Bldg 1520
Lab 329
Street address 1 Bethel Valley Road
City Oak Ridge
State/province Tennessee
ZIP/Postal code 37831-6342
Country New Zealand
 
Platform ID GPL15992
Series (1)
GSE40402 Clostridium thermocellum Transcriptomic Profiles after Exposure to Furfural or Heat Stress

Data table header descriptions
ID_REF
VALUE Loess normalized, average gene level intensity signal, log2 transformed

Data table
ID_REF VALUE
Cthe_0001P00032 11.5889038
Cthe_0001P00341 12.20214877
Cthe_0001P00600 12.49964303
Cthe_0001P00639 12.09400053
Cthe_0001P00934 12.75142517
Cthe_0001P01496 11.94043427
Cthe_0001P01513 12.44637737
Cthe_0002P00024 12.21987387
Cthe_0002P00033 12.1321483
Cthe_0002P00043 12.62530387
Cthe_0002P00136 11.99007273
Cthe_0002P00222 11.68901557
Cthe_0002P00473 12.46595167
Cthe_0002P00632 11.50391533
Cthe_0003P00219 11.44978627
Cthe_0003P00280 11.97052647
Cthe_0003P00466 11.32305653
Cthe_0003P00468 11.0627403
Cthe_0003P00470 11.07159573
Cthe_0003P00472 10.98246047

Total number of rows: 21335

Table truncated, full table size 575 Kbytes.




Supplementary file Size Download File type/resource
GSM1181939_296044_A1_Grid.pair.txt.gz 2.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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