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Links from GEO DataSets

Items: 20

1.

luxS-Dependent Gene Regulation in Escherichia coli K-12 Revealed by Genomic Expression Profiling (II)

(Submitter supplied) The bacterial quorum-sensing autoinducer 2 (AI-2) has received intense interest because the gene for its synthase, luxS, is common among a large number of bacterial species. We have identified luxS-controlled genes in Escherichia coli under two different growth conditions using DNA microarrays. Twenty-three genes were affected by luxS deletion in the presence of glucose, and 63 genes were influenced by luxS deletion in the absence of glucose. more...
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platform:
GPL199
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE9587
ID:
200009587
2.

luxS-Dependent Gene Regulation in Escherichia coli K-12 Revealed by Genomic Expression Profiling

(Submitter supplied) The bacterial quorum-sensing autoinducer 2 (AI-2) has received intense interest because the gene for its synthase, luxS, is common among a large number of bacterial species. We have identified luxS-controlled genes in Escherichia coli under two different growth conditions using DNA microarrays. Twenty-three genes were affected by luxS deletion in the presence of glucose, and 63 genes were influenced by luxS deletion in the absence of glucose. more...
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platform:
GPL199
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE9582
ID:
200009582
3.

Expression profile for early stationary phase E. coli W3110 expression profile

(Submitter supplied) Quorum signal uptake is an indispensable part of quorum sensing regulations. The coperative regulation of uptake repressor and kinase precisely signale the cells for quorum sensing uptake and terminate the quorum sensing signal production. We use the DNA microarray to detail the E. coli quorum sensing uptake reuglations and related gene regulations. Keywords: specific growth
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platform:
GPL199
6 Samples
Download data
Series
Accession:
GSE9203
ID:
200009203
4.

Expression data of Actinobacillus pleuropneumoniae 4074 and the ΔluxS mutant of Actinobacillus pleuropneumoniae 4074

(Submitter supplied) LuxS is an enzyme involved in the activated methyl cycle and the by-product autoinducer 2 (AI-2) was a quorum sensing signal in some species. In our previous study, the functional LuxS in AI-2 production was verified in the porcine respiratory pathogen Actinobacillus pleuropneumoniae. Enhanced biofilm formation and reduced virulence were observed in the luxS mutant. To comprehensively understand the luxS function, in this study, the transcriptional profiles were compared between the A. more...
Organism:
Actinobacillus pleuropneumoniae
Type:
Expression profiling by array
Platform:
GPL9691
16 Samples
Download data: TXT
Series
Accession:
GSE19056
ID:
200019056
5.

E. coli BW25113 yncC vs wt biofilm cells in LB 15h 37C and MG1655 yncC vs wt colony cells in LB plates 15h 37C

(Submitter supplied) E. coli K-12 BW25113 mutant strain yncC expression in biofilm cells relative to E. coli wild-type strain expression in biofilm cells. All samples were cultured in LB with glasswool at 37C for 15 hours and E. coli K-12 MG1655 mutant yncC colony cells vs wild type colony cells in LB plates 15h 37C. Quorum-sensing signal autoinducer 2 (AI-2) stimulates Escherichia coli biofilm formation through the motility regulator MqsR that induces expression of the putative transcription factor encoded by yncC. more...
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platforms:
GPL3154 GPL199
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE8706
ID:
200008706
6.

Escherichia coli K-12: luxS mutant LW12 vs. wild type W3110

(Submitter supplied) Transcripitonal profiling of Escherichia coli K-12 comparing luxS mutant LW12 with wild type W3110
Organism:
Escherichia coli
Type:
Expression profiling by array
Platform:
GPL8609
2 Samples
Download data: TXT
Series
Accession:
GSE20606
ID:
200020606
7.

Salmonella enterica Typhimurium grown with and without glucose

(Submitter supplied) Cell to cell communication in bacteria to regulate various cellular processes with respect to their population density is termed quorum sensing and is achieved using signaling molecules called autoinducers. LuxS, which is involved in the synthesis of the autoinducer molecule-2 (AI-2), is conserved in several Gram-positive and Gram-negative bacteria including the enteric pathogen Salmonella Typhimurium. more...
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. LT2; Salmonella enterica subsp. enterica serovar Typhi str. Ty2; Salmonella enterica subsp. enterica serovar Typhimurium; Salmonella enterica subsp. enterica serovar Typhi str. CT18
Type:
Expression profiling by array
Platforms:
GPL5096 GPL5069
44 Samples
Download data: GPR
Series
Accession:
GSE7558
ID:
200007558
8.

Expression data of S. mutans in semi synthetic medium with 0.5% sucrose

(Submitter supplied) The autoinducer-2 (AI-2) group of signalling molecules represent a new type of cell-cell communication since they are produced by many phylogenetic groups of bacteria as the by product of a metabolic transformation carried out by the luxS enzyme. To separate the metabolic function of the luxS enzyme from the signalling role of AI-2, we carried out a global transcriptome analysis of a luxS null mutant of Streptococcus mutans UA159, an important cariogenic bacterium and crucial component of the dental plaque biofilm community. more...
Organism:
Streptococcus mutans; Streptococcus mutans UA159
Type:
Expression profiling by array
Platform:
GPL4031
44 Samples
Download data
Series
Accession:
GSE5451
ID:
200005451
9.

Escherichia coli strain 8624 and Escherichia coli strain VS94 with signaling molecules

(Submitter supplied) These E. coli strains were grown with various signaling molecules and the expression profiles were determined. Keywords: addition of quorum and host hormone signals
Organism:
Escherichia coli
Type:
Expression profiling by array
Platform:
GPL3154
5 Samples
Download data: CEL, CHP
Series
Accession:
GSE7439
ID:
200007439
10.

AI-2-dependent gene regulation in Staphylococcus epidermidis

(Submitter supplied) Autoinducer 2 (AI-2), a widespread by-product of the LuxS-catalyzed S-ribosylhomocysteine cleavage reaction in the activated methyl cycle, has been suggested to serve as an intra- and interspecies signaling molecule, but in many bacteria AI-2 control of gene expression is not completely understood. Particularly, we have a lack of knowledge about AI-2 signaling in the important human pathogens Staphylococcus aureus and S. more...
Organism:
Coxiella burnetii; Rickettsia rickettsii; Chlamydia pneumoniae AR39; Borreliella burgdorferi B31; Coxiella burnetii RSA 493; Chlamydia trachomatis D/UW-3/CX; Staphylococcus epidermidis; Chlamydia muridarum; Staphylococcus epidermidis RP62A; Chlamydia caviae GPIC; Staphylococcus haemolyticus JCSC1435; Staphylococcus epidermidis ATCC 12228; Staphylococcus aureus subsp. aureus MW2; Granulibacter bethesdensis
Type:
Expression profiling by array
Platform:
GPL4692
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE9427
ID:
200009427
11.

Differential gene expression of ydgG mutant

(Submitter supplied) The E. coli Genechip antisense genome array was used to study the differential gene expression profile of E. coli K12 ydgG mutant compared to its isogenic wild type in a mature biofilm. Keywords: E. coli K12 antisense chip
Organism:
Escherichia coli K-12; Escherichia coli
Type:
Expression profiling by array
Platform:
GPL199
2 Samples
Download data
Series
Accession:
GSE3514
ID:
200003514
12.

AI-2 quorum sensing in *Yersinia pestis*

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platforms:
GPL10439 GPL10017
54 Samples
Download data: TXT
Series
Accession:
GSE30342
ID:
200030342
13.

Transcriptional analysis of temperature regulation in Yersinia pestis

(Submitter supplied) Temperature is a key environmental factor for facultative pathogens during the host adaptation response. To assess the functional role of temperature in Yersinia pestis, a microarray study was conducted comparing the Δpgm (pigmentation-negative) R88 strain grown at 37°C or 30°C.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10439
6 Samples
Download data: TXT
Series
Accession:
GSE30333
ID:
200030333
14.

Transcriptional analysis of AI-2 treatment in Yersinia pestis at 30°C

(Submitter supplied) Yersinia pestis, the etiological agent of plague, is able to sense cell density by quorum sensing. The function of quorum sensing in Y. pestis is not clear. Here, the process of autoinducer-2 (AI-2) quorum sensing was investigated by comparing transcript profiles when AI-2 quorum-sensing signal is added in to control. The strain Δpgm (pigmentation-negative) mutant was used as wild type.The control consisted of cells grown and treated under the same conditions without added signals.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10439
6 Samples
Download data: TXT
Series
Accession:
GSE30237
ID:
200030237
15.

3 quorum sensing signals add in microarray comparison in Yersinia pestis at 30°C

(Submitter supplied) The quorum-sensing system has been linked to diverse phenotypes and regulatory changes in pathogenic bacteria. In strain CO92, the AI-2 signal is produced in a luxS-dependent manner, reaching maximal levels of 2.5 μM in late logarithmic growth, and both wild type and pigmentation mutant strains made equivalent levels of AI-2. Yersinia pestis CO92 possesses a chromosomal lsr locus encoding factors involved in the binding and import of AI-2, and confirming this assignment, an lsr deletion increased extracellular pools of AI-2. more...
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10017
6 Samples
Download data: TXT
Series
Accession:
GSE30109
ID:
200030109
16.

LuxS/AI-2 quorum sensing microarray comparison in Yersinia pestis at 30°C

(Submitter supplied) The AI-2 quorum-sensing system has been linked to diverse phenotypes and regulatory changes in pathogenic bacteria. In strain CO92, the AI-2 signal is produced in a luxS-dependent manner, reaching maximal levels of 2.5 μM in late logarithmic growth, and both wild type and pigmentation mutant strains made equivalent levels of AI-2. Y. pestis CO92 possesses a chromosomal lsr locus encoding factors involved in the binding and import of AI-2, and confirming this assignment, an lsr deletion increased extracellular pools of AI-2. more...
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10017
6 Samples
Download data: TXT
Series
Accession:
GSE30108
ID:
200030108
17.

Transcriptional analysis of luxS-null strain in Yersinia pestis CO92 at 37°C

(Submitter supplied) Yersinia pestis, the etiological agent of plague, is able to sense cell density by quorum sensing. The function of quorum sensing in Y. pestis is not clear. Here, the process of autoinducer 2 (AI-2) quorum sensing was investigated by comparing transcript profiles when luxS gene was knocked out. The luxS gene encodes S-ribosylhomocysteinase which can produce DPD, a precursor of AI-2. The strain ∆pgm (pigmentation-negative) mutant R88 was called wild type. more...
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10439
6 Samples
Download data: TXT
Series
Accession:
GSE22849
ID:
200022849
18.

Transcription analysis of AI-2 signal add in experiment in Yersinia pestis CO92 at 37°C

(Submitter supplied) Yersinia pestis, the etiological agent of plague, is able to sense cell density by quorum sensing. The function of quorum sensing in Y. pestis is not clear. Here, the process of autoinducer-2 (AI-2) quorum sensing was investigated by comparing transcript profiles when AI-2 quorum-sensing signal is added in. The strain ∆pgm(pigmentation-negative) mutant R88 was used as wild type. The control consisted of cells grown and treated under the same conditions without added signals.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10439
6 Samples
Download data: TXT
Series
Accession:
GSE22848
ID:
200022848
19.

Transcriptional analysis of AHLs signals add in experiment inYersinia pestis CO92 at 37°C

(Submitter supplied) Yersinia pestis, the etiological agent of plague, is able to sense cell density by quorum sensing. The function of quorum sensing in Y. pestis is not clear. Here, the process of AHL quorum sensing was investigated by comparing transcript profiles when two AHL quorum-sensing signals are added in. The strain ∆pgm (pigmentation-negative) mutant R88 was called wild type. The two AHLs signals are N-(3-Oxooctanoyl)-L-homoserine lactone and N-Hexanoyl-DL-homoserine lactone.The control consisted of cells grown and treated under the same conditions without added signals.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10439
6 Samples
Download data: TXT
Series
Accession:
GSE22847
ID:
200022847
20.

Transcriptional analysis of three quorum sensing signals add in experiment inYersinia pestis CO92 at 37°C

(Submitter supplied) Yersinia pestis, the etiological agent of plague, is able to sense cell density by quorum sensing. The function of quorum sensing in Y. pestis is not clear. Here, the process of quorum sensing was investigated by comparing transcript profiles when three quorum-sensing signals are added in. The strain ∆pgm (pigmentation-negative) mutant R88 was used as wild type. The three signals are AI-2, AHLs (N-(3-Oxooctanoyl)-L-homoserine lactone and N-Hexanoyl-DL-homoserine lactone).The control consisted of cells grown and treated under the same conditions without added signals.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10439
6 Samples
Download data: TXT
Series
Accession:
GSE22846
ID:
200022846
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