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SRX9405712: GSM4874062: S12_30min_2; Shewanella decolorationis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 8.3M spots, 1.7G bases, 1.2Gb downloads

Submitted by: NCBI (GEO)
Study: Molecular mechanism of zero valent iron-enhanced microbial azo reduction in Shewanella decolorationis S12
show Abstracthide Abstract
Here, we established a successive Fe0-enhanced microbe system to remove azo dye (a typical organic pollutant) by Shewanella decolorationis S12 (S. decolorationis S12, an effective azo dye degradation bacterium) and examined the gene expression time course (10, 30, 60, and 120 min) in whole genome transcriptional level. Comparing with the treatment without ZVI, approximately 8% genes affiliated with 10 different gene expression profiles in S. decolorationis S12 were significantly changed in 120 min during the ZVI-enhanced microbial azo reduction. Intriguingly, MarR transcriptional factor might play a vital role in regulating ZVI-enhanced azo reduction in the aspect of energy production, iron homeostasis, and detoxification. Further investigation showed that induced [Ni-Fe] H2ase genes (hyaABCDEF) and azoreductase genes (mtrABC-omcA) contributed to ZVI-enhanced energy production, while reduced iron uptake (hmuVCB and feoAB), induced sulfate assimilation (cysPTWA) and cysteine biosynthesis (cysM) related genes were essential to iron homeostasis and detoxification. This study disentangles underlying mechanisms of ZVI-enhanced azo reduction in S. decolorationis S12 and lays a foundation for further optimization of integrated ZVI-microbial system for efficient organic pollution treatment. Overall design: mRNA profiles of Shewanella decoloriationis S12 treated/untreated with Fe0 for 10, 30, 60, and 120 min were generated by deep sequencing, in triplicate, using Illumina Hiseq 2000.
Sample: S12_30min_2
SAMN16605539 • SRS7623150 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA from the cell pellet was isolated using a TRIzol Reagent kit (Invitrogen, Carlsbad, USA) following the manufacturer's instructions. RNA samples were treated with RNase-free DNaseI (QIAGEN, Carlsbad, USA) to digest residual genomic DNA and then purified by an RNeasy kit (Qiagen, Valencia, USA). Ribosomal RNA was removed by a RiboZero™ rRNA Removal kit (Epicenter, Madison, USA) following the manufacturer's protocols (Bhagwat et al., 2014). RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM4874062
Links:
Runs: 1 run, 8.3M spots, 1.7G bases, 1.2Gb
Run# of Spots# of BasesSizePublished
SRR129526188,285,6121.7G1.2Gb2021-10-02

ID:
12278000

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