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Series GSE21402 Query DataSets for GSE21402
Status Public on Oct 01, 2010
Title Expression analysis of Sphingomonas paucimobilis sp. EPA505 during biodegradation kinetics of various PAHs and detection of gene in a contaminated soil S3
Platform organism Sphingomonas paucimobilis
Sample organisms Sphingomonas paucimobilis; uncultured organism
Experiment type Expression profiling by array
Summary Studying eight enzymes involved in the degradation of polycyclic aromatic hydrocarbons from the model strain Sphingomonas paucimobilis sp. EPA505 using a designed microarray of 8,048 probes. During the biodegradation kinetics with phenanthrene, fluoranthene or a mix of both pollutants, we identified the targeted set of genes induced by these pollutants, compared to basal expression detected with glucose.
Hybridizing total DNA extracted from S3, we show the efficiency of our probe design to study a complex environment. Despite the relative small size of our probes (23-mers), their sensitivity is reliable as we can detect the presence of genes in this complex mixture.
Obtained results are further described in Sébastien Terrat, Eric Peyretaillade, Olivier Gonçalves, Eric Dugat-Bony, Fabrice Gravelat, and Pierre Peyret. 2010 - Studying the ‘Unkown’ with Metabolic Design, a new probe design software for explorative functional microarrays development. Nucleic Acids Research (submited).
 
Overall design A 17 chip study was realized using total RNA recovered from separate cultures of Sphingomonas paucimobilis sp. EPA505 with phenanthrene, fluoranthene or a mix of these both pollutants as sole carbon and energy source. A negative kinetic expermient was realized with glucose as sole carbon and energy source. Each chip measures the expression level of 8 genes from Sphingomonas paucimobilis sp. EPA505 with 23-mer probes (a total of 8,048 probes) using a new design approach. We also assess metabolic capacities of microbial communities in an aromatic hydrocarbons contaminated soil named S3. Each probe was spotted in triplicate, and a total of 8,863 random probes was used to determine the background noise.
 
Contributor(s) TERRAT S, PEYRETAILLADE E, GONCALVES O, DUGAT-BONY E, GRAVELAT F, PEYRET P
Citation(s) 20860850
Submission date Apr 20, 2010
Last update date Mar 22, 2012
Contact name TERRAT Sebastien
E-mail(s) sebastien.terrat@gmail.com
Phone 33(0)473407604
Fax 33(0)473407670
Organization name UMR CNRS 6023
Department Génomique Intégrée des Interactions Microbiennes
Lab Laboratoire Microorganismes : Génome et Environnement
Street address 24, avenue des Landais, Campus des Cézeaux
City AUBIERE
ZIP/Postal code 63171
Country France
 
Platforms (1)
GPL10343 Nimblegen_Custom_PAH_array_V01
Samples (17)
GSM534815 EPA505_Glucose_3h
GSM534816 EPA505_Glucose_6h
GSM534817 EPA505_Glucose_10h
Relations
BioProject PRJNA126403

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE21402_RAW.tar 188.4 Mb (http)(custom) TAR (of PAIR)
Processed data included within Sample table

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