GEO DataSets

(Submitter supplied) Active segregation of DNA in bacteria is catalyzed by cytomotive structures. Mediators of subcellular plasmid positioning are Walker-type ATPases (ParA), actin-like proteins, or tubulin homologs. These motor proteins are coupled to the DNA via adaptor proteins that recognize specific DNA motifs. Here, we describe that a temperate phage, CGP3, integrated into the genome of Corynebacterium glutamicum ATCC 13032 encodes an actin-like protein, AlpC. more...

Organism:

Escherichia coli; Corynebacterium glutamicum; Corynebacterium glutamicum ATCC 13032; Bacillus subtilis subsp. subtilis str. 168; Gluconobacter oxydans

Type:

Expression profiling by array

Platform:

GPL16988

3 Samples

Download data: GPR

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.

Organism:

Escherichia coli; Corynebacterium glutamicum; Bacillus subtilis subsp. subtilis str. 168; Gluconobacter oxydans; Corynebacterium glutamicum ATCC 13032

Type:

Expression profiling by array

Platforms:

GPL16988 GPL16989

9 Samples

Download data: GPR

(Submitter supplied) Active segregation of DNA in bacteria is catalyzed by cytomotive structures. Mediators of subcellular plasmid positioning are Walker-type ATPases (ParA), actin-like proteins, or tubulin homologs. These motor proteins are coupled to the DNA via adaptor proteins that recognize specific DNA motifs. Here, we describe that a temperate phage, CGP3, integrated into the genome of Corynebacterium glutamicum ATCC 13032 encodes an actin-like protein, AlpC. more...

Organism:

Escherichia coli; Corynebacterium glutamicum; Corynebacterium glutamicum ATCC 13032; Bacillus subtilis subsp. subtilis str. 168; Gluconobacter oxydans

Type:

Expression profiling by array

Platform:

GPL16989

6 Samples

Download data: GPR

(Submitter supplied) DNA microarrays were applied to investigate the transcriptome of C. glutamicum cells and to identify potential target genes under CgpS countersilencing conditions. The silencing activity of CgpS was reduced by overexpression of the N-terminal part, which was placed under the control of the inducible tac promoter in the pAN6 plasmid. The expression of the N terminal part was induced with 100 µM IPTG.

Organism:

Corynebacterium glutamicum; Gluconobacter oxydans; Bacillus subtilis subsp. subtilis str. 168; Escherichia coli

Type:

Expression profiling by array

Platform:

GPL20268

3 Samples

Download data: GPR