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SRX8644577: GSM4647855: PolyA RNA ONS Rep 1; Lemna gibba; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 71.3M spots, 14.4G bases, 9.4Gb downloads

Submitted by: NCBI (GEO)
Study: Integrated metabolic and transcriptomic analysis of the duckweed Lemna gibba growing under photomixotrophic conditions: Metabolic adjustments to different nitrogen sources
show Abstracthide Abstract
Duckweeds are small, rapidly growing aquatic flowering plants. Due to their ability for biomass production at high rates they represent promising candidates for biofuel feedstocks. Duckweeds are also excellent model organisms because they can be maintained in well-defined liquid media, usually reproduce asexually, and because genomic resources are becoming increasingly available. To establish a framework for quantitative metabolic research in duckweeds we derived a central carbon metabolism network model of Lemna gibba based on its draft genome. Lemna gibba fronds were grown in a photomixotrophic mode in liquid media under continuous light with 13C-labeled glucose as a carbon source. Two different conditions (nitrate vs. glutamine as nitrogen source) were compared by quantification of growth kinetics, metabolite levels, metabolic flux and transcript abundance. Overall design: Fronds grown on inorganic nitrogen (nitrate) or on organic nitrogen (glutamine) medium were harvested and immediately frozen in liquid nitrogen. For each condition three biological replicates were analyzed.
Sample: PolyA RNA ONS Rep 1
SAMN15411686 • SRS6935767 • All experiments • All runs
Organism: Lemna gibba
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Fronds grown on inorganic nitrogen or on organic nitrogen medium were harvested and immediately frozen in liquid nitrogen. For each condition three biological replicates were analyzed. Total RNA was extracted by grinding 200 mg frozen tissue to a fine powder in liquid nitrogen with a mortar and pestle, followed by extraction with TRIzol Reagent (Invitrogen) and ethanol precipitation. Total RNA was resuspended and treated with RQ1 RNase-free DNase (Promega) on an RNA Clean & Concentrator-5 column (Zymo). The purity and concentration of RNA were determined by a NanoDrop Nd-1000 spectrophotometer (Thermo Scientific) and a Qubit fluorometer (Qiagen). Polyadenylated RNA was enriched from total RNA with the Dynabeads mRNA Purification Kit (Life Technologies). Indexed, directional RNA-seq libraries were prepared with ScriptSeq v2 reagents (Epicentre) from 40-50 ng of polyA-selected RNA according to the manufacturer's instructions. Libraries were sequenced on an Illumina HiSeq 2000 instrument generating 101bp paired-end reads.
Experiment attributes:
GEO Accession: GSM4647855
Links:
Runs: 1 run, 71.3M spots, 14.4G bases, 9.4Gb
Run# of Spots# of BasesSizePublished
SRR1212327571,261,01614.4G9.4Gb2023-09-14

ID:
11233955

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