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SRX9915766: Near full-length 16S rRNA gene amplicon sequencing of culture BP, originating from a freshwater sediment core
1 PACBIO_SMRT (Sequel) run: 20,635 spots, 52.9M bases, 34Mb downloads

Design: DNA was extracted using the DNEasy UltraClean Microbial Kit (QIAGEN, Hilden, Germany), according to the user's manual. Two rounds of PCR were applied for DNA amplification. The first PCR was performed using the KAPA HiFi ReadyMix PCR Kit (KAPABioSystems, Cape Town, South Africa) and universal primer-tailed 16S primers (27F /5AmMC6/ gcagtcgaacatgtagctgactcaggtcac AGRGTTYGATYMTGGCTCAG, 1492R /5AmMC6/ tggatcacttgtgcaagcatcacatcgtag RGYTACCTTGTTACGACTT) (Biomers.net, Ulm, Germany), followed by purification with the QIAquick PCR purification kit (QIAGEN, Hilden, Germany). The second PCR was performed using the KAPA HiFi ReadyMix PCR Kit and PacBio Barcoded Universal F/R Primers Plate 96 (Pacific Biosciences, California, USA), followed by AMPure PB bead kit (PacBio biosciences, California, USA) purification. The SMRTbell library preparation and further purification were achieved by SMRTbell Template Prep Kit (PacBio biosciences, California, USA).
Submitted by: University of Tuebingen
Study: Multi-omics of the nitrate-reducing iron(II)-oxidizing culture BP
show Abstracthide Abstract
Nitrate-reducing iron(II)-oxidizing (NDFO) bacteria are widespread in the environment contribute to nitrate removal and influence the fate of the greenhouse gases nitrous oxide and carbon dioxide. The autotrophic growth of nitrate-reducing iron(II)-oxidizing bacteria is rarely investigated and poorly understood. The most prominent model system for this type of studies is enrichment culture KS, which originates from a freshwater sediment in Bremen, Germany. A second NDFO culture, culture BP, was obtained with a sample taken in 2015 at the same pond and cultured in a similar way. To gain insights in the metabolism of nitrate reduction coupled to iron(II) oxidation under in the absence of organic carbon and oxygen limited conditions, we performed metagenomic, metatranscriptomic and metaproteomic analyses of culture BP.This dataset contains: (1) Raw sequencing data of 16S (V4 region, primers 515f and 806r) rRNA amplicon sequencing of the microbial community composition of the autotrophic NRFeOx enrichment culture BP and of environmental samples from the pond where culture BP originates from. Illumina MiSeq sequencing (Illumina, San Diego, CA, USA) using PE 250 bp MiSeq Reagent Kit v2 (500 cycles kit) were performed at Microsynth AG (Balgach, Switzerland). (2) Raw sequencing data of near full-length 16S (primers 27F and 1492R) sequenced with PacBio Sequel SMRT at the Helmholtz research institute, Munich, Germany. (3) Raw sequencing data of shotgun metagenomics. Library was prepared with TruSeq DNA PCR-Free Kit (Illumina) and sequenced with PE 150 bp on a NovaSeq 6000 totalling 91 Gbp by CeGaT, Tuebingen, Germany. (4) Short reads were assembled with MEGAHIT v1.2.7 using https://github.com/nf-core/mag v1.0.0. (5) Raw sequencing data of shotgun metatranscriptomes (2 conditions, triplicates). Library preparation including bacterial ribodepletion (Illumina Stranded Total RNA Prep with Ribo-Zero Plus kit) and Illumina NextSeq v2.5 sequencing with PE 75 bp and 6 to 53 Mio clusters per sample were performed by Microsynth AG (Balgach, Switzerland).
Sample: Near full-length 16S rRNA gene amplicon sequencing of culture BP, originating from a freshwater sediment core
SAMN17492611 • SRS8092972 • All experiments • All runs
Library:
Name: Y2lbc94
Instrument: Sequel
Strategy: AMPLICON
Source: METAGENOMIC
Selection: PCR
Layout: SINGLE
Runs: 1 run, 20,635 spots, 52.9M bases, 34Mb
Run# of Spots# of BasesSizePublished
SRR1350409920,63552.9M34Mb2021-05-17

ID:
12975261

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