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SRX23231235: GSM8019124: AP64, 4 hours after the shift to light, dark control rep1; Gemmatimonas phototrophica; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 7.2M spots, 673.1M bases, 204.4Mb downloads

External Id: GSM8019124_r1
Submitted by: Laboratory of Anoxygenic Phototrophs, Centre Algatech, Institute of Microbiology Czech Acad. Sci.
Study: Transcriptional response of Gemmatimonas phototrophica to changing light regimes [AP64_LowLight]
show Abstracthide Abstract
In this study, we provide a time-series analysis of the transcriptional response of Gemmatimonas phototrophica AP64T during the dark-to-light transition under aerobic and semiaerobic conditions. By analysing its transcriptome, focussing especially on PS-related genes, we tested the hypothesis that G. phototrophica might constitute an example of an anoxygenic phototroph on its evolutionary pathway from anaerobic to aerobic life-style. Overall design: G. phototrophica AP64T (= DSM 29774) was grown in an optimized liquid medium described earlier (Shivaramu et al., 2023) at 25°C. At the beginning of each experiment, the inoculum (approx. OD600 = 0.2) was diluted in 100 mL of a fresh medium to approx. OD600 = 0.03. Cultures were grown in triplicates aerobically in the dark until reaching approx. OD600 = 0.2. Then cultures were illuminated with photon flux density of 100 µmol photons m-2 s-1. Sampling was done 2, 4, and 8 hours after the light was switched on. Control cultures were kept in dark and sampled for each time point as a reference.
Sample: AP64, 4 hours after the shift to light, dark control rep1
SAMN39459290 • SRS20153966 • All experiments • All runs
Library:
Name: GSM8019124
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Cells from triplicate cultures were harvested by centrifugation, resuspended in 1 mL PGTX extraction solution (Pinto et al., 2009) and immediately frozen in liquid nitrogen. RNA was extracted as described earlier (Kopejtka et al., 2020). Libraries were generated according to the protocol of Shishkin et al. (2015) including rRNA removal with the RiboZero Kit (Illumina, USA) and sequenced on a NovaSeq 6000 (Illumina, USA) in paired-end mode with 100 cycles in total.
Runs: 1 run, 7.2M spots, 673.1M bases, 204.4Mb
Run# of Spots# of BasesSizePublished
SRR275620877,160,785673.1M204.4Mb2024-02-01

ID:
31393192

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