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Items: 1 to 20 of 9592

1.

Broad-spectrum tolerance to disinfectant-mediated bacterial killing due to mutation of the PheS aminoacyl tRNA synthetase

(Submitter supplied) Disinfectants are essential tools for controlling infectious diseases and maintaining sterile conditions in many medical and food-industry settings. Recent work revealed that a deficiency in the PTS carbohydrate phosphor transfer system confers pan-tolerance to killing by diverse disinfectant types through its interaction with the cAMP-CRP regulatory network. The present work characterized a new pan-tolerance mutant obtained by enrichment using phenol as a lethal probe and an Escherichia coli PTS null mutant as a parental strain. more...
Organism:
Escherichia coli K-12
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26856
4 Samples
Download data: TXT
Series
Accession:
GSE282610
ID:
200282610
2.

Genetic properties underlying transcriptional plasticity and evolvability in E. coli

(Submitter supplied) The rate and direction of phenotypic evolution depends on the availability of phenotypic variants induced either genetically or environmentally for selection act upon. Theoretical suggest that genetic interactions between genes governing phenotypes could explain how the bias in phenotypic variability arises. However, it remains unknown whether the phenotypic variability is explained by real known genetic interactions as expected. more...
Organism:
Escherichia coli str. K-12 substr. MG1655; Escherichia coli
Type:
Expression profiling by array
Platform:
GPL18948
16 Samples
Download data: TXT
Series
Accession:
GSE260863
ID:
200260863
3.

Highly multiplexed spatial transcriptomics in bacteria

(Submitter supplied) Single-cell decisions made in complex environments underlie many bacterial phenomena. Image-based, transcriptomics approaches offer an avenue to study such behaviors, yet these approaches have been hindered by the massive density of bacterial mRNA. To overcome this challenge, we combine 1000-fold volumetric expansion with multiplexed error robust fluorescence in situ hybridization (MERFISH) to create bacterial-MERFISH, a method enabling high-throughput, spatially resolved profiling of thousands of operons within individual bacteria. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21117 GPL26592
3 Samples
Download data: FASTA, SF
Series
Accession:
GSE268480
ID:
200268480
4.

Chaperone saturation mediates translation and protein folding efficiency

(Submitter supplied) Whether the emergence of a nascent protein from the ribosome and the formation of structural elements are synchronized has been a longstanding question. Paradoxically, kinetically efficient translation can induce mis-folding and aggregation despite the presence of molecular chaperones, which in Escherichia coli are induced by unfolded protein via σ32. The molecular mechanisms mediating translation efficiency and protein folding efficiency remain poorly understood. more...
Organism:
Escherichia coli str. K-12 substr. MG1655; Escherichia coli
Type:
Other; Expression profiling by high throughput sequencing
Platforms:
GPL18956 GPL18133
30 Samples
Download data: TSV
Series
Accession:
GSE104303
ID:
200104303
5.

Ribosome collisions trigger subunit splitting in E. coli

(Submitter supplied) Although many clinically important antibiotics inhibit bacterial ribosomes, the mechanisms by which bacterial cells rescue ribosomes stalled by antibiotics remain poorly understood. Ribosome stalling leads to collisions that recruit ribosome quality control (RQC) factors that recycle the ribosome subunits and target nascent proteins for degradation. Surprisingly, loss of known RQC factors in E. coli does not lead to significant antibiotic sensitivity, even though antibiotics stall ribosomes and induce collisions, suggesting the existence of additional, uncharacterized RQC mechanisms. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL21117
6 Samples
Download data: WIG
Series
Accession:
GSE270401
ID:
200270401
6.

RNC-seq of S1K247Q and S1WT

(Submitter supplied) RNC-seq experiment of the simulated acetylation mutant S1K247Q of S1 protein
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26592
6 Samples
Download data: TXT
Series
Accession:
GSE254167
ID:
200254167
7.

RNA-seq of S1K247Q and S1WT

(Submitter supplied) RNA-seq experiment of the simulated acetylation mutant S1K247Q of S1 protein
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26592
6 Samples
Download data: TXT
Series
Accession:
GSE254165
ID:
200254165
8.

Genome concentration limits cell growth and modulates proteome composition in Escherichia coli

(Submitter supplied) Defining the cellular factors that drive growth rate and proteome composition is essential for understanding and manipulating cellular systems. In bacteria, ribosome concentration is known to be a constraining factor of cell growth rate, while gene concentration is usually assumed not to be limiting. Here, using single-molecule tracking, quantitative single-cell microscopy, and modeling, we show that genome dilution in Escherichia coli cells arrested for DNA replication results in a decrease in the concentration of active RNA polymerases and ribosomes. more...
Organism:
Caulobacter vibrioides; Escherichia coli K-12
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34296
8 Samples
Download data: BIGWIG
Series
Accession:
GSE261497
ID:
200261497
9.

De novo gene synthesis by an antiviral reverse transcriptase

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other; Expression profiling by high throughput sequencing
Platform:
GPL21117
75 Samples
Download data: BED, BW
Series
Accession:
GSE270164
ID:
200270164
10.

De novo gene synthesis by an antiviral reverse transcriptase [RNA-seq]

(Submitter supplied) Bacteria defend themselves from viral predation using diverse immune systems, many of which sense and target foreign nucleic acids. Defense-associated reverse transcriptase (DRT) systems provide an intriguing counterpoint to this immune strategy by instead leveraging DNA synthesis, but the identities and functions of their DNA products remain largely unknown. Here we show that DRT2 systems execute an unprecedented immunity mechanism that involves de novo gene synthesis via rolling-circle reverse transcription of a non-coding RNA (ncRNA). more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21117
3 Samples
Download data: BED
Series
Accession:
GSE270162
ID:
200270162
11.

De novo gene synthesis by an antiviral reverse transcriptase [RIP-seq]

(Submitter supplied) Bacteria defend themselves from viral predation using diverse immune systems, many of which sense and target foreign nucleic acids. Defense-associated reverse transcriptase (DRT) systems provide an intriguing counterpoint to this immune strategy by instead leveraging DNA synthesis, but the identities and functions of their DNA products remain largely unknown. Here we show that DRT2 systems execute an unprecedented immunity mechanism that involves de novo gene synthesis via rolling-circle reverse transcription of a non-coding RNA (ncRNA). more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL21117
36 Samples
Download data: BW
Series
Accession:
GSE270161
ID:
200270161
12.

De novo gene synthesis by an antiviral reverse transcriptase [cDIP-seq]

(Submitter supplied) Bacteria defend themselves from viral predation using diverse immune systems, many of which sense and target foreign nucleic acids. Defense-associated reverse transcriptase (DRT) systems provide an intriguing counterpoint to this immune strategy by instead leveraging DNA synthesis, but the identities and functions of their DNA products remain largely unknown. Here we show that DRT2 systems execute an unprecedented immunity mechanism that involves de novo gene synthesis via rolling-circle reverse transcription of a non-coding RNA (ncRNA). more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL21117
36 Samples
Download data: BW
Series
Accession:
GSE270160
ID:
200270160
13.

The DNA damage response of Escherichia coli: differential gene expression after replication inhibition by azidothymidine

(Submitter supplied) We examined the DNA damage response of bacterium E. coli using the replication inhibitor azidothyimdine (AZT), and RNA-Seq analysis. We confirm the induction of classic SOS loci by AZT and identify several genes, including many of the pyrimidine pathway, that are induced dependent on LexA cleavage, but have not been previously demonstrated to be DNA damage-inducible. Despite a strong dependence on LexA, these genes lack LexA boxes and their regulation by LexA is likely to be indirect via unknown factors. more...
Organism:
Escherichia coli K-12
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24020
16 Samples
Download data: TSV
Series
Accession:
GSE263906
ID:
200263906
14.

RNA polymerase stalling-derived genome instability underlies ribosomal antibiotic efficacy and resistance evolution

(Submitter supplied) Bacteria often evolve antibiotic resistance through mutagenesis. However, the processes causing the mutagenesis have not been fully resolved. Here we found that a broad range of ribosome-targeting antibiotics caused mutations through an underexplored pathway. Focusing on the clinically important aminoglycoside gentamicin, we found that the translation inhibitor caused genome-wide premature stalling of RNA polymerase (RNAP) in a loci-dependent manner. more...
Organism:
Escherichia coli BW25113
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27123
24 Samples
Download data: CSV, XLSX
Series
Accession:
GSE240474
ID:
200240474
15.

Systematic Study on the Three-Dimensional Genome of Escherichia Coli and Its Thermal Adaptation Mechanism (RNA-Seq)

(Submitter supplied) Total RNA was extracted and sequenced from Escherichia coli cultured to log phase and stable phase at 37 ° C and 45 ° C, respectively. The transcriptome data of Escherichia coli under four different growth conditions were obtained.
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24659
12 Samples
Download data: TXT
Series
Accession:
GSE211824
ID:
200211824
16.

Systematic Study on the Three-Dimensional Genome of Escherichia Coli and Its Thermal Adaptation Mechanism (3C-Seq)

(Submitter supplied) Chromosome conformation capture and sequencing experiments were carried out at 37℃ and 45℃ for E. coli in logarithmic phase and stable phase, respectively. Three-dimensional DNA interaction data of E. coli under four different growth conditions and control group were obtained
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL24659
10 Samples
Download data: TXT
Series
Accession:
GSE211823
ID:
200211823
17.

Spatial Chromosome Organization and Adaptation of Escherichia coli under Heat Stress

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24659
22 Samples
Download data: TXT
Series
Accession:
GSE211825
ID:
200211825
18.

Genome-scale CRISPRi screen identifies pcnB repression conferring improved physiology for overproduction of free fatty acids in Escherichia coli II

(Submitter supplied) Microbial physiology plays a pivotal role in construction of a superior microbial cell factory for efficient production of desired products. Here we identified pcnB repression through genome-scale CRISPRi modulation combining fluorescence-activated cell sorting (FACS) and next-generation sequencing (NGS), which confers improved physiology for free fatty acids (FFAs) overproduction in Escherichia coli. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL26592
5 Samples
Download data: XLSX
Series
Accession:
GSE267827
ID:
200267827
19.

Genome-scale CRISPRi screen identifies pcnB repression conferring improved physiology for overproduction of free fatty acids in Escherichia coli

(Submitter supplied) Microbial physiology plays a pivotal role in construction of a superior microbial cell factory for efficient production of desired products. Here we identified pcnB repression through genome-scale CRISPRi modulation combining fluorescence-activated cell sorting (FACS) and next-generation sequencing (NGS), which confers improved physiology for free fatty acids (FFAs) overproduction in Escherichia coli. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34485
6 Samples
Download data: XLS
Series
Accession:
GSE267710
ID:
200267710
20.

Motility-activating mutations upstream of flhDC reduce acid shock survival of Escherichia coli

(Submitter supplied) Many neutralophilic bacterial species try to evade acid stress with an escape strategy, which is reflected in the increased expression of genes coding for flagellar components. Extremely acid-tolerant bacteria, such as Escherichia coli, survive the strong acid stress, e.g. in the stomach of vertebrates. Recently, we were able to show that the induction of motility genes in E. coli is strictly dependent on the degree of acid stress, i.e. more...
Organism:
Escherichia coli BW25113; Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL32899 GPL34252
12 Samples
Download data: XLSX
Series
Accession:
GSE260455
ID:
200260455
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