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Series GSE287362 Query DataSets for GSE287362
Status Public on Jan 21, 2025
Title Gross transcriptomic analysis of Pseudomonas putida for diagnosing environmental shifts
Organism Pseudomonas putida KT2440
Experiment type Expression profiling by high throughput sequencing
Summary The biological regime of Pseudomonas putida (and any other bacterium) under given environmental conditions results from the hierarchical expression of sets of genes that become turned on and off in response to one or more physicochemical signals. In some cases, such signals are clearly defined, but in many others, cells are exposed to a whole variety of ill-defined inputs that occur simultaneously. Transcriptomic analyses of bacteria passed from a reference condition to a complex niche can thus expose both the type of signals that they experience during the transition and the functions involved in adaptation to the new scenario. In this article, we describe a complete protocol for generation of transcriptomes aimed at monitoring the physiological shift of P. putida between two divergent settings using as a simple case study the change between homogeneous, planktonic lifestyle in a liquid medium and growth on the surface of an agar plate. To this end, RNA was collected from P. putidaKT2440 cells at various times after growth in either condition, and the genome-wide transcriptional outputs were analysed. While the role of individual genes needs to be verified on a case-by-case basis, a gross inspection of the resulting profiles suggested cells that are cultured on solid media consistently had a higher translational and metabolic activity, stopped production of flagella and were conspicuously exposed to a strong oxidative stress. The herein described methodology is generally applicable to other circumstances for diagnosing lifestyle determinants of interest.
 
Overall design 100 microL of an over night culture of Pseudomonas putida KT2440 was cultured in M9 minimal media supplemented with 0.2 % (v/w) citrate in the following conditions: 5 mL of liquid media during 6 hours, 12 hours or 24 hours incubation, and solid media (25 mL of 1.5% (v/w) agar plate) during 6 hours, 12 hours or 24 hours incubation. RNA was collected and sent for RNASeq service in two biological replicates per condition. Each time point ( 6, 12 and 24 hours) were used to contrast results for liquid and solid media in order to check what genes are transcribed differentially in cells exposed to a solid surface vs cells that live in a liquid media.
 
Contributor(s) Hueso-Gil Á, Calles B, O'Toole GA, de Lorenzo V
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Submission date Jan 17, 2025
Last update date Jan 21, 2025
Contact name Ángeles Hueso-Gil
E-mail(s) [email protected]
Phone +34915854517
Organization name Centro Nacional de Biotecnología (CNB, CSIC)
Department Systems Biology
Lab Environmental Microbiology
Street address c/ Darwin 3
City Madrid
State/province Madrid
ZIP/Postal code 28049
Country Spain
 
Platforms (1)
GPL25301 Illumina HiSeq 2500 (Pseudomonas putida KT2440)
Samples (12)
GSM8744910 Pseudomonas putida KT2440, liquid media, 6 hours, rep1
GSM8744911 Pseudomonas putida KT2440, liquid media, 6 hours, rep2
GSM8744912 Pseudomonas putida KT2440, solid media, 6 hours, rep1
Relations
BioProject PRJNA1212213

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Supplementary file Size Download File type/resource
GSE287362_SOL12hvsLIQ12h_Annotated_modif.csv.gz 362.9 Kb (ftp)(http) CSV
GSE287362_SOL24hvsLIQ24h_Annotated_modif.csv.gz 398.6 Kb (ftp)(http) CSV
GSE287362_SOL6hvsLIQ6h_Annotated_modif.csv.gz 366.9 Kb (ftp)(http) CSV
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