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SRX6035827: GSM3872526: RTK17.1_O2-limited_N-limited (N2) [RTK171121216]; Methylacidiphilum sp. RTK17.1; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 8.6M spots, 1.7G bases, 887.1Mb downloads

Submitted by: NCBI (GEO)
Study: Hydrogen metabolism influences glycogen production in a verrucomicrobial methanotroph
show Abstracthide Abstract
Metabolic flexibility in aerobic methane oxidising bacteria (methanotrophs) enhances cell growth and survival in instances where resources are variable or limiting. Examples include the production of intracellular compounds (such as glycogen or polyhydroxyalkanoates) in response to unbalanced growth conditions and the use of some energy substrates, besides methane, when available. Indeed, recent studies show that verrucomicrobial methanotrophs can grow mixotrophically through oxidation of hydrogen and methane gases via respiratory membrane-bound group 1d [NiFe] hydrogenases and methane monooxygenases respectively. Hydrogen metabolism is particularly important for adaptation to methane and oxygen limitation, suggesting this metabolic flexibility may confer growth and survival advantages. In this work, we provide evidence that, in adopting a mixotrophic growth strategy, the thermoacidophilic methanotroph, Methylacidiphilum sp. RTK17.1 changes its growth rate, biomass yields and the production of intracellular glycogen reservoirs. Under nitrogen-fixing conditions, removal of hydrogen from the feed-gas resulted in a 14 % reduction in observed growth rates and a 144% increase in cellular glycogen content. Concomitant with increases in glycogen content, the total protein content of biomass decreased following the removal of hydrogen. Transcriptome analysis of Methylacidiphilum sp. RTK17.1 revealed a 3.5-fold upregulation of the Group 1d [NiFe] hydrogenase in response to oxygen limitation and a 4-fold upregulation of nitrogenase encoding genes (nifHDKENX) in response to nitrogen limitation. Genes associated with glycogen synthesis and degradation were expressed constitutively and did not display evidence of transcriptional regulation. Collectively these data further challenge the belief that hydrogen metabolism in methanotrophic bacteria is primarily associated with energy conservation during nitrogen fixation and suggests its utilisation provides a competitive growth advantage within hypoxic habitats. Overall design: Chemostat cell samples (5 total) of Methylacidiphilum sp. RTK17,1 were grown methanotrophically under oxygen excess and oxygen limiting conditions in the presence of NH4+ or N2 as a usable nitrogen source with or without hydrogen gas supplementation into the feedgas
Sample: RTK17.1_O2-limited_N-limited (N2) [RTK171121216]
SAMN12012267 • SRS4939162 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: isolation of mRNA was performed using the RNeasy Mini kit (Qiagen) according to the manufacturer's protocol. Following total RNA extraction, ribosomal RNAs were removed using the Ribo-Zero rRNA removal kit (bacteria) and the quality of the remaining RNA was assessed using an Agilent 2100 Bioanalyzer (Agilent). Ribo-Zero User Guide, TruSeq Stranded Total RNA prep
Experiment attributes:
GEO Accession: GSM3872526
Links:
Runs: 1 run, 8.6M spots, 1.7G bases, 887.1Mb
Run# of Spots# of BasesSizePublished
SRR92654908,639,5061.7G887.1Mb2019-10-03

ID:
8078578

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