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SRX992515: GSM1656362: F1 21 h aerobic; Lactobacillus buchneri CD034; RNA-Seq
1 ILLUMINA (Illumina HiSeq 1000) run: 38.5M spots, 1.9G bases, 1.1Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Differential Analysis of L. buchneri Transcriptomes under anaerobic and aerobic conditions
show Abstracthide Abstract
The Lactobacillus buchneri CD034 strain, known to improve the ensiling process of green fodder and the quality of the silage itself was transcriptionally analyzed by sequencing of transcriptomes isolated under anaerobic vs. aerobic conditions. L. buchneri CD034 was first cultivated under anaerobic conditions and then shifted to aerobic conditions by aeration with 21% oxygen. Cultivations already showed that oxygen was consumed by L. buchneri CD034 after aeration of the culture while growth of L. buchneri CD034 was still observed. RNA sequencing data revealed that irrespective of the oxygen status of the culture, the most abundantly transcribed genes are required for basic cell functions such as protein biosynthesis, energy metabolism and lactic acid fermentation. Under aerobic conditions, 283 genes were found to be transcriptionally up-regulated while 198 genes were found to be down-regulated (p-value < 0.01). Up-regulated genes i. a. play a role in oxygen consumption via oxidation of pyruvate or lactate (pox, lctO). Additionally, genes encoding proteins required for decomposition of reactive oxygen species (ROS) such as glutathione reductase or NADH peroxidase were also found to be up-regulated. Genes related to pH homeostasis and redox potential balance were found to be down-regulated under aerobic conditions. Overall, genes required for lactic acid fermentation were hardly affected by the growth conditions applied. Genes identified to be differentially transcribed depending on the aeration status of the culture are suggested to specify the favorable performance of the strain in silage formation. Overall design: 2 samples, 2 replicates
Sample: F1 21 h aerobic
SAMN03481146 • SRS907229 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 1000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Cells were mechanically lyzed using Lysing Maxtrix B lysis tubes (MP Biomedicals). RNA was extracted applying the QIAGEN RNeasy kit. mRNA was enriched applying the RiboZero Bacteria kit. Libraries were created applying the Illumina TruSeq Stranded mRNA Library Prep Kit according to the manufacturers protocol.
Experiment attributes:
GEO Accession: GSM1656362
Links:
External link:
Runs: 1 run, 38.5M spots, 1.9G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR197066338,470,2161.9G1.1Gb2017-02-10

ID:
1440331

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