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Links from GEO DataSets

Items: 10

1.

cAMP phosphodiesterase CpdA of Corynebacterium glutamicum: identification, characterization, influence on cAMP level, growth, and global expression, and transcriptional activation by GlxR

(Submitter supplied) DNA microarrays were applied to investigate the effect of cpdA deletion (del) or overexpression (over) on the global gene expression of C. glutamicum cells. For overexpression of cpdA the gene was cloned into plasmid pEKEx2 under control of the IPTG-inducible tac promoter, which was induced by addition of 250 µM IPTG.
Organism:
Escherichia coli; Bacillus subtilis subsp. subtilis str. 168; Corynebacterium glutamicum; Gluconobacter oxydans
Type:
Expression profiling by array
Platform:
GPL20268
6 Samples
Download data: GPR
Series
Accession:
GSE81004
ID:
200081004
2.

Chip-chip from C. glutamicum wild type expressing GlxR tagged with Strep Tag II and cyaB deletion strain expressing GlxR tagged with Strep Tag II.

(Submitter supplied) Corynebacterium glutamicum GlxR is a homolog of the cAMP receptor protein. Although over 200 GlxR binding sites in the C. glutamicum genome are predicted in silico, studies on the GlxR physiological function have been hindered by the severe growth defects of a glxR mutant. This study comprehensively identified the GlxR regulon by chromatin immunoprecipitation in conjunction with microarray (ChIP-chip) analyses. more...
Organism:
Corynebacterium glutamicum
Type:
Genome binding/occupancy profiling by array
Platform:
GPL11651
7 Samples
Download data: GPR
Series
Accession:
GSE26870
ID:
200026870
3.

The influence of acetate in the medium to the global gene expression of C. glutamicum wild type (WT) and the C. glutamicum ΔcyaB mutant (ΔcyaB)

(Submitter supplied) The cAMP-dependent transcriptional regulator GlxR serves as a central hub in the regulatory network of the actinobacterial model organism Corynebacterium glutamicum and controls expression of ~10% of all genes. The consequences of a lowered cAMP level are mostly unkown. A single gene (cyaB) for a cAMP-synthesizing adenylate cyclase was identified and it had been reported that a cyaB mutant grows like the wild type on glucose, but has a strong growth defect in the presence of acetate. more...
Organism:
Corynebacterium glutamicum ATCC 13032
Type:
Expression profiling by array
Platform:
GPL9860
3 Samples
Download data: GPR, XLSX
Series
Accession:
GSE140408
ID:
200140408
4.

Comparison of Corynebacterium glutamicum ATCC13032ΔftsR with ATCC13032

(Submitter supplied) In summary, we have identified and characterized FtsR as a transcriptional activator of the essential cell division protein FtsZ in C. glutamicum, providing a novel regulatory player in the process of cell division.
Organism:
Escherichia coli; Corynebacterium glutamicum; Corynebacterium glutamicum ATCC 13032; Bacillus subtilis subsp. subtilis str. 168; Gluconobacter oxydans
Type:
Expression profiling by array
Platform:
GPL16989
3 Samples
Download data: GPR
Series
Accession:
GSE107921
ID:
200107921
5.

Regulation of the pstSCAB operon in Corynebacterium glutamicum by the regulator of acetate metabolism RamB

(Submitter supplied) <Background> The pstSCAB operon of Corynebacterium glutamicum, which encodes an ABC transport system for uptake of phosphate (Pi), is induced during the P i starvation response. The two-component regulatory system PhoRS is involved in this response, but partial Pi starvation induction of pstSCAB in a ∆phoRS mutant indicated the involvement of additional regulator(s). Regulation of pstSCAB also involves the global transcriptional regulator GlxR. more...
Organism:
Corynebacterium glutamicum ATCC 13032
Type:
Expression profiling by array
Platform:
GPL19905
2 Samples
Download data: CSV
Series
Accession:
GSE67012
ID:
200067012
6.

RNA sequencing of ATCC 17978hm Acineotbacter baumannii strain and CpdA mutant

(Submitter supplied) Difference in RNA expression levels between Acinetobacter baumannii cells expressing high and low levels of cyclic AMP
Organism:
Acinetobacter baumannii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19644
2 Samples
Download data: TXT
Series
Accession:
GSE64935
ID:
200064935
7.

Determination of transcriptional start sites in the presence of GABA for Corynebacterium glutamicum

(Submitter supplied) In this study, we analyzed the regulation of ƴ-aminobutyrate (GABA) utilization in Corynebacterium glutamicum by the PucR-type transcriptional regulator GabR and by alternative nitrogen and carbon sources.
Organism:
Corynebacterium glutamicum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29058
1 Sample
Download data: XLS
Series
Accession:
GSE156688
ID:
200156688
8.

Comparison of Corynebacterium glutamicum

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Gluconobacter oxydans; Pseudomonas putida; Corynebacterium glutamicum; Escherichia coli; Bacillus subtilis subsp. subtilis str. 168
Type:
Expression profiling by array
Platform:
GPL22794
8 Samples
Download data: GPR
Series
Accession:
GSE138829
ID:
200138829
9.

Comparison of Corynebacterium glutamicum with GABA or glucose as carbon source

(Submitter supplied) γ-Aminobutyric acid (GABA) is a non-proteinogenic amino acid and widespread in nature from microorganisms to plants and animals. DNA microarray analysis revealed that the transcription of gabTDP was strongly increased in C. glutamicum wild type grown with GABA and urea compared to the same strain cultivated with glucose and urea. Remarkably, the presence of ammonia partially inhibited growth on GABA, and the reasons for it were also investigated in this study.
Organism:
Escherichia coli; Corynebacterium glutamicum; Bacillus subtilis subsp. subtilis str. 168; Pseudomonas putida; Gluconobacter oxydans
Type:
Expression profiling by array
Platform:
GPL22794
4 Samples
Download data: GPR
Series
Accession:
GSE138828
ID:
200138828
10.

Comparison of C. glutamicum growing with GABA as carbon source in the presence or absence of (NH4)2SO4.

(Submitter supplied) γ-Aminobutyric acid (GABA) is a non-proteinogenic amino acid and widespread in nature from microorganisms to plants and animals. DNA microarray analysis revealed that the transcription of gabTDP was strongly increased in C. glutamicum wild type grown with GABA and urea compared to the same strain cultivated with glucose and urea. Remarkably, the presence of ammonia partially inhibited growth on GABA, and the reasons for it were also investigated in this study.
Organism:
Pseudomonas putida; Gluconobacter oxydans; Escherichia coli; Corynebacterium glutamicum; Bacillus subtilis subsp. subtilis str. 168
Type:
Expression profiling by array
Platform:
GPL22794
4 Samples
Download data: GPR
Series
Accession:
GSE138827
ID:
200138827
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