U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX8130226: GSM4483500: NH4_lim; Candidatus Kuenenia stuttgartiensis; RNA-Seq
3 ILLUMINA (Illumina MiSeq) runs: 4.8M spots, 648.1M bases, 356.5Mb downloads

Submitted by: NCBI (GEO)
Study: Transcriptome Kuenenia stuttgartiensis bioreactor
show Abstracthide Abstract
Anaerobic ammonium-oxidising (anammox) bacteria, members of the 'Candidatus Brocadiaceae' family, play an important role in the nitrogen cycle and are estimated to be responsible for about half of the oceanic nitrogen loss to the atmosphere. Anammox bacteria combine ammonium with nitrite and produce dinitrogen gas via the intermediates nitric oxide and hydrazine (anammox reaction) while nitrate is formed as a by-product. These reactions take place in a specialized, membrane-bound compartment called the anammoxosome. Therefore, the substrates ammonium, nitrite and product nitrate have to cross the outer-, cytoplasmic- and anammoxosome membranes to enter or exit the anammoxosome. The genomes of all anammox species harbour multiple copies of ammonium-, nitrite- and nitrate transporter genes. Here we investigated how the distinct genes for ammonium-, nitrite- and nitrate- transport were expressed during substrate limitation in membrane bioreactors. Transcriptome analysis of Kuenenia stuttgartiensis planktonic cells under ammonium-limitation showed that three of the seven ammonium transporter genes and one of the six nitrite transporter genes were significantly upregulated, while another ammonium and nitrite transporter gene were downregulated in nitrite limited growth conditions. The two nitrate transporters were expressed to similar levels in both conditions. In addition, genes encoding enzymes involved in the anammox reaction were differentially expressed, with those using nitrite as a substrate being upregulated under nitrite limited growth and those using ammonium as a substrate being upregulated during ammonium limitation. Taken together, these results give a first insight in the potential role of the multiple nutrient transporters in regulating transport of substrates and products in and out of the compartmentalized anammox cell. Overall design: triplicate samples, two conditions.
Sample: NH4_lim
SAMN14611145 • SRS6493838 • All experiments • All runs
Library:
Instrument: Illumina MiSeq
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was isolated using both the TRIzol™ Reagent and the RiboPure™ bacteria kit (ThermoFisher Scientific, Waltham, USA) according to the manufacturer's instructions with the exception that 100-fold higher cell numbers were used, since the recommended cell number resulted in very low to no RNA yields. RNA was eluted in DEPC treated water in volumes between 20-25 μl for the TRIzol™ method and 50-70 μl for the RiboPure™ method, of which 1-2 μl was used to quantify the isolated RNA. The isolated RNA was treated with DNAse 1, as described and provided by the RiboPure™ kit. cDNA libraries were made using TruSeq stranded mRNA Library Prep Kit v2, according to the protocol supplied by the manufacturer (Illumina, San Diego, California U.S.A.).
Experiment attributes:
GEO Accession: GSM4483500
Links:
Runs: 3 runs, 4.8M spots, 648.1M bases, 356.5Mb
Run# of Spots# of BasesSizePublished
SRR115607011,392,051189.2M103.7Mb2020-04-21
SRR115607021,438,254198.1M109.9Mb2020-04-21
SRR115607031,944,723260.8M143Mb2020-04-21

ID:
10580221

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...