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SRX23536693: GSM8064136: Pss9644, experimental, HMM, rep 2; Pseudomonas syringae pv. syringae; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 11.7M spots, 3.5G bases, 1Gb downloads

External Id: GSM8064136_r1
Submitted by: University of Birmingham
Study: Transcriptome profiling of Pseudomonas syringae pv. syringae 9644 in rich media and hrp-inducing minimum media
show Abstracthide Abstract
Pseudomonas syringae pv. syringae 9644 (Pss9644) is a causal agent of bacterial cherry canker causing necrotic symptoms on leaves, fruits, gummosis and canker in woody tissues of sweet cherry (Prunus avium). To understand which virulent factor genes were expressed in vitro, Pss9644 was grown in rich media (King's B Broth) and minimum media (hrp-inducing minimum media). The latter mimics the in planta environment. Overall design: Pss9644 was grown in King's B broth overnight. Later, it was diluted (OD= 0.1) until grown to log phase (OD=0.6). Cells were washed and shaking incubated in King's B broth and hrp-inducing minimum media Cells were harvested after 5 hours post incubation. Total RNA was extracted. RNA samples underwent ribosomal depletion before sequencing.
Sample: Pss9644, experimental, HMM, rep 2
SAMN39832742 • SRS20385185 • All experiments • All runs
Library:
Name: GSM8064136
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA extraction protocol performed according to Moreno-Lopez et al. 2021 (https://doi.org/10.3390/microorganisms9071447) RNA was converted atNovogeneinto sequencing-ready libraries for Illumina sequencing using Illumina Ribo-Zero Plus rRNA Depletion Kit andNovogeneNGS Stranded RNA Library Prep Set (PT044)*. cDNA libraries were subjected to RNASeq, using an Illumina Novaseq 6000 system with 150-bp pair-end reads. Prokaryotic directional mRNA preparation (rRNA removal)
Runs: 1 run, 11.7M spots, 3.5G bases, 1Gb
Run# of Spots# of BasesSizePublished
SRR2787481111,657,2673.5G1Gb2024-04-07

ID:
31794091

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