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Links from GEO DataSets

Items: 20

1.

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
2.

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
3.

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
4.

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:
GPL199 GPL3154
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE8706
ID:
200008706
5.

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
6.

Indole cell signaling occurs primarily at low temperatures in Escherichia coli

(Submitter supplied) We have shown the quorum-sensing signals acylhomoserine lactones (AHLs), autoinducer-2 (AI-2), and indole influence the biofilm formation of Escherichia coli. Here, we investigate how the environment, i.e., temperature, affects indole and AI-2 signaling in E. coli. We show in biofilms that indole addition leads to more extensive differential gene expression at 30°C (186 genes) than at 37°C (59 genes), that indole reduces biofilm formation (without affecting growth) more significantly at 25°C and 30°C than at 37°C, and that the effect is associated with the quorum-sensing protein SdiA. more...
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platforms:
GPL3154 GPL199
14 Samples
Download data: CEL, CHP
Series
Accession:
GSE9923
ID:
200009923
7.

E. coli K-12 yliH and yceP biofilm expression relative to wild type

(Submitter supplied) Expression in biofilm cells of mutants yceP and yliH relative to biofilm cells of E. coli K-12 wild type strain Keywords: comparison of strain expression profiles
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platform:
GPL199
4 Samples
Download data
Series
Accession:
GSE3937
ID:
200003937
8.

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
9.

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
10.

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
11.

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
12.

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
13.

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
14.

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
15.

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
16.

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
17.

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
18.

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
19.

Transcriptional analysis of quorum sensing deficient 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 quorum sensing was investigated by comparing transcript profiles when three quorum-sensing synthase genes are knocked out. Two strains, ∆pgm (pigmentation-negative) mutant R88 as treatment and quorum sensing null strain R115 with mutations (∆pgm, ∆ypeIR, ∆yspIR, and ∆luxS) as control, are used in this analysis.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10439
6 Samples
Download data: TXT
Series
Accession:
GSE21911
ID:
200021911
20.

Transcriptional analysis of quorum sensing null strain in Yersinia pestis CO92 at 30°C

(Submitter supplied) Yersinia pestis is the etiology of plague that 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 synthase genes are knocked out. Two strains, ∆pgm (pigmentation-negative) mutant R88 as treatment and 3XQS mutant with mutation (∆pgm, ∆ypeIR, ∆yspIR, and ∆luxS) R115 as control are used in this analysis.
Organism:
Yersinia pestis
Type:
Expression profiling by array
Platform:
GPL10017
6 Samples
Download data: TXT
Series
Accession:
GSE20217
ID:
200020217
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