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Items: 1 to 20 of 508

1.

Complete Genome Sequencing and Transcriptome Analysis of aniline-degrading strain T1

(Submitter supplied) The aniline-degrading strain T1 can efficiently degrade aniline, however, it is not clear which key genes are associated with aniline degradation, and we have adopted a genome-wide and transcriptomic approach to fully understand the microbial degradation mechanism of aniline.
Organism:
Pseudomonas veronii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34605
6 Samples
Download data: TXT
Series
Accession:
GSE269992
ID:
200269992
2.

Differential expression of Pseudomonas fluorescens SBW25 during growth using glucose or MHPP as carbon sources

(Submitter supplied) Identify genes involved in catabolism of the compound Methyl 3-(4-hydroxyphenyl)propionate
Organism:
Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33279
8 Samples
Download data: CSV
Series
Accession:
GSE228022
ID:
200228022
3.

Role of quorum sensing of Hafnia alvei H4 in co-culture with Pseudomonas fluorescens ATCC13525 analyzed by biological and transcriptomic

(Submitter supplied) transcriptomics was used to explore the regulation mechanism of QS in dual-species spoilage at mRNA molecular level.
Organism:
Hafnia alvei; Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33855
6 Samples
Download data: TXT
Series
Accession:
GSE245811
ID:
200245811
4.

Evolutionary innovation through transcription factor rewiring in microbes is shaped by levels of transcription factor activity, expression, and existing connectivity

(Submitter supplied) The survival of a population during environmental shifts depends on whether the rate of phenotypic adaptation keeps up with the rate of changing conditions. A common way to achieve this is via change to gene regulatory network (GRN) connections – known as rewiring – that facilitate novel interactions and innovation of transcription factors. To understand the success of rapidly adapting organisms, we therefore need to determine the rules that create and constrain opportunities for GRN rewiring. more...
Organism:
Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29078
15 Samples
Download data: CSV, TXT
Series
Accession:
GSE228016
ID:
200228016
5.

YAMAT-seq of mature tRNA pools in the bacterium Pseudomonas fluorescens SBW25 and derivatives.

(Submitter supplied) Mature tRNA pools were measured using an adaptation of YAMAT-seq (Shigematsu et al., 2017; doi:10.1093/nar/gkx005 ) and further described in (Ayan et al., 2020; doi:10.7554/eLife.57947) in eight strains dervied from the model bacterium, Pseudomonas fluorescens SBW25. The aim of the experiment was to determine the effect on the mature tRNA pool of (i) removing multi-copy tRNA genes by genetic engineering, and (ii) duplicating tRNA genes during a subsequent, compensatory evolution experiment. more...
Organism:
Pseudomonas fluorescens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL28120
24 Samples
Download data: XLSX
Series
Accession:
GSE196705
ID:
200196705
6.

The ColR/S two-component system is a conserved determinant of host association across Pseudomonas species

(Submitter supplied) Members of the bacterial genus Pseudomonas form associations with diverse hosts. Comparative transcriptomics revealed that the ColR regulon has diverged between P. aeruginosa and P. fluorescens and deleting components of the ColR regulon revealed strain-specific, but not host-specific, requirements for ColR-dependent genes.
Organism:
Pseudomonas aeruginosa; Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21297 GPL31044
24 Samples
Download data: TXT
Series
Accession:
GSE190448
ID:
200190448
7.

Virulence, cellular masking, and grazing resistance in the struggle to survive under long term protozoan predation; the genetics of survival

(Submitter supplied) Purpose: Generalist protozoan predators change the pace of evolution in microbial communities, but investigations into the molecular consequences of predation for the genomic evolution of defence or coadaptation are scarce. We have previously performed a 90-day co-evolution experiment to address these effects using the bacterium Pseudomonas fluorescens SBW25 on solid media in the presence and absence of a wild Acanthamoeba sp. more...
Organism:
Acanthamoeba sp.; Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL32161 GPL28120
24 Samples
Download data: TXT
Series
Accession:
GSE206989
ID:
200206989
8.

Dynamic mode decomposition of transcriptome dynamics and optimal sensor placement for discovery of genetic reporters

(Submitter supplied) Accelerating the design of synthetic biological circuits for biosensing requires expanding the currently available genetic toolkit. Although whole-cell biosensors have been successfully engineered and deployed, particularly in applications such as environmental and medical diagnostics, novel sensing applications necessitate the discovery and optimization of novel biosensors. Here we develop a data-driven approach that combines dynamic mode decomposition and observability analysis to extract salient, endogenous genetic sensors for analytes of interest from dynamic gene expression profiles. more...
Organism:
Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL31044
40 Samples
Download data: JSON, TSV
Series
Accession:
GSE200822
ID:
200200822
9.

Protozoan predation drives rapid adaptive divergence by selecting for tuned cellulose production and amyloid fibrils in Pseudomonas fluorescens SBW25

(Submitter supplied) Purpose: Protozoan predators affect the structure of bacterial communities, but investigations into how predation influences bacterial evolution and antagonistic behaviours are scarce. We performed a 20-day predator-prey evolution experiment on solid media to investigate the adaptive traits that arise in bacterial prey under continuous protozoan predation. Methods: Pseudomonas fluorescens SBW25 and a wild Acanthamoeba sp. more...
Organism:
Acanthamoeba sp.; Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL32161 GPL28120
24 Samples
Download data: TXT
Series
Accession:
GSE200723
ID:
200200723
10.

Next Generation Sequencing Facilitates Quantitative Analysis of Transcriptomes of Wild Type and invF Deficient Mutant of Pseudomonas fluorescens 2P24

(Submitter supplied) InvF, an AraC-type transcriptional activator, regulated the expression of genes that encoded the secreted effector molecules SipABCD, SigD, SptP, and SopE in Salmonella typhimurium. However, it seems that almost all effector homologs were lost in P. fluorescens 2P24. To identify the InvF regulon in strain 2P24, the invF deficient mutant 2P24ΔinvF was constructed, and we implemented transcriptome sequencing (RNA-seq). more...
Organism:
Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30468
12 Samples
Download data: TXT
Series
Accession:
GSE181272
ID:
200181272
11.

Convergent transcriptional responses to acquisition and amelioration of different conjugative plasmids

(Submitter supplied) Aim: to identify the transcriptional responses to acquisition of conjugative megaplasmids by Pseudomonas fluorescens, and how these effects are impacted by known compensatory mutations. Full abstract TBC.
Organism:
Pseudomonas [fluorescens] SBW25
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28611
30 Samples
Download data: CSV
Series
Accession:
GSE151570
ID:
200151570
12.

Identifying candidate genes whose expression is regulated by CbrAB and NtrBC in Pseudomonas fluorescens SBW25

(Submitter supplied) Histidine is a good source of nutrient for many bacteria, but its utilization poses a significant challenge as it delivers excess nitrogen over carbon. The rate of histidine catabolism (hut) must thus be tightly regulated. Here, in Pseudomonas fluorescens SBW25, we show that the CbrAB two-component system directly activates the transcription of hut genes, while mediating succinate-induced carbon catabolite repression of hut at the translational level via the CbrAB-CrcYZ-Hfq/Crc regulatory cascade. more...
Organism:
Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28231
2 Samples
Download data: CSV
Series
Accession:
GSE160152
ID:
200160152
13.

YAMAT-seq of mature tRNA pools in the bacterium Pseudomonas fluorescens SBW25 and derivatives

(Submitter supplied) Mature tRNA pools were measured using an adaptation of Y-shaped Adapter-ligated MAture tRNA sequencing (YAMAT-seq) (Shigematsu et al., 2017) in nine strains derived from the model bacterium, Pseudomonas fluorescens SBW25. The aim of the experiment was to determine the effect on the mature tRNA pool of (i) removing the single-copy serCGA gene by genetic engineering, and (ii) duplicating the serTGA gene during a subsequent, compensatory evolution experiment. more...
Organism:
Pseudomonas fluorescens
Type:
Other
Platform:
GPL28120
27 Samples
Download data: XLSX
Series
Accession:
GSE144791
ID:
200144791
14.

Determination of carbon metabolism response regulators regulons in several Pseudomonas species by DAP-seq

(Submitter supplied) We identified binding sites genome-wide for carbon metabolism transcriptional response regulators in Pseudomonas stutzeri RCH2, Pseudomonas putida KT2240, Pseudomonas fluorescens FW300-N2E2 and FW300-N2C3 by DNA-affinity-purified (DAP) sequencing.
Organism:
Pseudomonas fluorescens; Pseudomonas putida; Stutzerimonas stutzeri
Type:
Other
Platforms:
GPL29080 GPL29079 GPL29078
96 Samples
Download data: WIG
Series
Accession:
GSE157075
ID:
200157075
15.

Iron deficiency response of interactions between Brachypodium and Pseudomonas fluorescens SBW25 under controlled growth conditions.

(Submitter supplied) The goal of this study was to evaluate the molecular mechanisms by which Brachypodium distachyon grown with and without Pseudomonas fluorescens (P. fluorescens) strain SBW25 respond to Fe deprivation. Fe deprivation induced Brachypodium secretion of phytosiderophores and reduced biomass production while inoculation with P. fluorescens resulted in alterations of extracellular metabolite abundances. Results provide insight into the role of iron in interactions between a host plant and root associated bacteria.
Organism:
Pseudomonas fluorescens; Brachypodium distachyon
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL29168 GPL29167
30 Samples
Download data: TXT
Series
Accession:
GSE158273
ID:
200158273
16.

Identifying candidate genes whose expression is regulated by the HutC transcriptional repressor in Pseudomonas fluorescens SBW25

(Submitter supplied) HutC in Pseudomonas is a representative member of the HutC/GntR family of transcriptional regulators, which possess a N-terminal winged helix-turn-helix (wHTH) DNA-binding domain and a C-terminal substrate binding domain. HutC is generally known to represses expression of histidine utilization (hut) genes through binding to the PhutU promoter with urocanate (the first intermediate of the histidine degradation pathway) as the direct inducer. more...
Organism:
Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28231
2 Samples
Download data: CSV
Series
Accession:
GSE146488
ID:
200146488
17.

RNA-seq data showing the effects of rpoD mutation t1682c in Pseudomonas fluorescens

(Submitter supplied) We report RNA-seq data for four Pseudomonas fluorescens SBW25 types: SBW25 (wild type) and dervied types 6A4, 6B4-Cap- and 6B4-Cap+. The aim of the study is to see the effect of a mutation in rpoD (carried by 6B4) on the transcriptome.
Organism:
Pseudomonas [fluorescens] SBW25
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25322
12 Samples
Download data: TXT
Series
Accession:
GSE116490
ID:
200116490
18.

Definition of global transcriptional variation in wild type Pseudomonas fluorescens Pf0-1 and its phosphorothioate modification (PT) deficient mutant by RNA-seq analysis

(Submitter supplied) To determine whether PT modifications are involved in the epigenetic control of specific genes, RNA-seq analysis was conducted to define global transcriptional changes in early log-phase cultures of wild-type pf0-1 and the PT modifacation related genes(dndBCDE) deletion mutant TT-5. Compared with wild-type pf0-1, a total of ten genes in TT-5 exhibited differential expression of greater than 2-fold (log2-ratio>1 or <-1, p-value<0.05, FDR≤0.001), including 6 up-regulated genes and 4 down-regulated genes (Table 1). more...
Organism:
Pseudomonas fluorescens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24598
2 Samples
Download data: XLS
Series
Accession:
GSE110489
ID:
200110489
19.

Divalent cations promote the transfer of the IncP-7 plasmid pCAR1 among different Pseudomonas hosts

(Submitter supplied) An incompatibility P-7 plasmid pCAR1 can be efficiently transferred among artificial microcosms in the presence of divalent cations Ca2+ and Mg2+. One on one mating assays between Pseudomonas strains with different plasmids showed that the promotion of transfer efficiency by divalent cations was also found in other plasmids including pB10 and NAH7, whereas the impacts were larger in IncP-7 plasmids. more...
Organism:
Pseudomonas; Pseudomonas fluorescens Pf0-1; Pseudomonas putida KT2440
Type:
Expression profiling by genome tiling array
Platforms:
GPL8298 GPL8296 GPL6591
24 Samples
Download data: BAR, CEL
Series
Accession:
GSE97565
ID:
200097565
20.

Transcriptional responses of Pseudomonas veronii 1YdBTEX2 to the exposure to laboratory induced matric and solute stresses

(Submitter supplied) We study the transcriptional reactions of bacteria interesting for biodegradation under laboratory conditions that mimic water stress. We compared the transcriptomes of cultures growing exponential phase under optimal conditions versus their responses to an osmotic shock of 30 min in exponential phase. The osmotic shock consisted in a reduction of water potential induced by salt (NaCl, solute stress) or by polyethylene glycol (PEG8000, matric stress). more...
Organism:
Pseudomonas veronii 1YdBTEX2
Type:
Expression profiling by array
Platform:
GPL20216
12 Samples
Download data: TXT
Series
Accession:
GSE69022
ID:
200069022
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