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Status |
Public on Jan 08, 2016 |
Title |
Expression profile of Pseudomonas aeruginosa ΔgcsR PAO1 using RNA-Seq |
Organism |
Pseudomonas aeruginosa |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
The TyrR-like enhancer-binding protein GcsR (or PA2449) was shown to regulate the expression of genes required for glycine metabolism. In order to define the regulon of GcsR we compared the transcriptome of a gcsR deletion mutant of P. aeruginosa PAO1 with that of the wild-type using RNA-Seq.
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Overall design |
Strains were grown under glycine rich conditions (peptone broth) and their transcriptomes were compared using RNA-Seq.
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Contributor(s) |
Sarwar Z, Nomura CT |
Citation(s) |
27303730 |
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Submission date |
Jan 04, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Christopher T Nomura |
E-mail(s) |
[email protected]
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Phone |
315-470-6854
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Organization name |
SUNY-ESF
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Department |
Chemistry
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Lab |
336 Jahn
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Street address |
1 Forestry Dr.
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City |
Syracuse |
State/province |
New York |
ZIP/Postal code |
13210 |
Country |
USA |
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Platforms (1) |
GPL21297 |
Illumina NextSeq 500 (Pseudomonas aeruginosa) |
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Samples (4)
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Relations |
BioProject |
PRJNA307608 |
SRA |
SRP068065 |