|
Status |
Public on Apr 01, 2021 |
Title |
SC-BactRS-12S-SCR-342_S8_R1_001 |
Sample type |
SRA |
|
|
Source name |
∆chvI chvI(D52E)++
|
Organism |
Caulobacter vibrioides |
Characteristics |
strain: CB15 genotype: delta_chvI xylX::pMT585-chvI(D52E)
|
Growth protocol |
2 mL PYE cultures were inoculated with ∆chvI EV and ∆chvI chvI(D52E)++ cells and grown overnight. Cultures were diluted to OD660 = 0.001 in 2 mL fresh PYE and grown for 22.5 hours. Cultures were diluted to OD660 = 0.075 in 5 mL PYE + 0.15% xylose and grown for 3.5 hours before TRIzol extraction.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated from C. crescentus cell pellets using TRIzol per manufacturer protocol, followed by purification with a Qiagen RNeasy kit. RNA-seq libraries were prepared using an Illumina TruSeq stranded RNA kit and sequenced on an Illumina NextSEQ500 instrument
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|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
FastQ files from Illumina NextSEQ500 were processed using the CLC genomics workbench (Qiagen) RNA-seq data analysis pipeline. Reads were mapped to the coding regions of the Caulobacter crescentus NA1000 genome (accession CP001340) Genome_build: GenBank accession CP001340 Supplementary_files_format_and_content: Processed files report the results of expression analysis in CLC Genomics Workbench in tab-delimited .txt format.
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|
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Submission date |
Mar 15, 2021 |
Last update date |
Apr 02, 2021 |
Contact name |
Sean Crosson |
E-mail(s) |
[email protected]
|
Phone |
5178845345
|
Organization name |
Michigan State University
|
Department |
Dept. Microbiology and Molecular Genetics
|
Street address |
567 Wilson Rd
|
City |
East Lansing |
State/province |
Michigan |
ZIP/Postal code |
48824 |
Country |
USA |
|
|
Platform ID |
GPL24555 |
Series (1) |
GSE168965 |
Defining the transcriptional regulon of ChvI in Caulobacter crescentus |
|
Relations |
BioSample |
SAMN18315631 |
SRA |
SRX10348158 |