Christophe Collet

Dr. Christophe Collet

orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 November 2004 in International Journal of Hydrogen Energy
Verified
Journal Article
Closed access
CCChristophe Collet
Christophe Collet

1 June 2019 in Materials Today Communications
Verified
Journal Article
Closed access
AVAlankar A. Vaidya
Alankar A. Vaidya
CCChristophe Collet
Christophe Collet
MGMarc Gaugler
Marc Gaugler
GLGareth Lloyd-Jones
Gareth Lloyd-Jones

4 August 2017 in The ISME Journal
Verified
Journal Article
Open access
PDF file
CCCarlo R Carere
Carlo R Carere
KHKiel Hards
Kiel Hards
KHKaren M Houghton
Karen M Houghton
JPJean F Power
Jean F Power
BMBen McDonald
Ben McDonald
MSMatthew Stott
Matthew Stott
Aerobic methanotrophic bacteria have evolved a specialist lifestyle dependent on consumption of methane and other short-chain carbon compounds. However, their apparent substrate specialism runs contrary to the high relative abundance of these microorganisms in dynamic environments, where the availability of methane and oxygen fluctuates. In this work, we provide in situ and ex situ evidence that verrucomicrobial methanotrophs are mixotrophs. Verrucomicrobia-dominated soil communities from an acidic geothermal field in Rotokawa, New Zealand rapidly oxidised methane and hydrogen simultaneously. We isolated and characterised a verrucomicrobial strain from these soils, Methylacidiphilum sp. RTK17.1, and showed that it constitutively oxidises molecular hydrogen. Genomic analysis confirmed that this strain encoded two [NiFe]-hydrogenases (group 1d and 3b), and biochemical assays revealed that it used hydrogen as an electron donor for aerobic respiration and carbon fixation. While the strain could grow heterotrophically on methane or autotrophically on hydrogen, it grew optimally by combining these metabolic strategies. Hydrogen oxidation was particularly important for adaptation to methane and oxygen limitation. Complementary to recent findings of hydrogenotrophic growth by Methylacidiphilum fumariolicum SolV, our findings illustrate that verrucomicrobial methanotrophs have evolved to simultaneously utilise hydrogen and methane from geothermal sources to meet energy and carbon demands where nutrient flux is dynamic. This mixotrophic lifestyle is likely to have facilitated expansion of the niche space occupied by these microorganisms, allowing them to become dominant in geothermally influenced surface soils. Genes encoding putative oxygen-tolerant uptake [NiFe]-hydrogenases were identified in all publicly available methanotroph genomes, suggesting hydrogen oxidation is a general metabolic strategy in this guild.

1 August 2005 in Journal of Biotechnology
Verified
Journal Article
Closed access
CCChristophe Collet
Christophe Collet
OGOlivier Gaudard
Olivier Gaudard
PPPaul Péringer
Paul Péringer
JSJean-Paul Schwitzguébel
Jean-Paul Schwitzguébel

16 August 2019 in Frontiers in Microbiology
Verified
Journal Article
Open access
CCCarlo Robert Carere
Carlo Robert Carere
BMBen McDonald
Ben McDonald
HPHanna A. Peach
Hanna A. Peach
CGChris Greening
Chris Greening
DGDaniel J. Gapes
Daniel J. Gapes
MSMatthew B. Stott
Matthew B. Stott
Metabolic flexibility in aerobic methane oxidizing 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 utilization provides a competitive growth advantage within hypoxic habitats.

1 October 2003 in Journal of Applied Microbiology
Verified
Journal Article
Open access
PDF file
CCChristophe Collet
Christophe Collet
JSJ.-P. Schwitzguebel
J.-P. Schwitzguebel
PPP. Peringer
P. Peringer
Aims: The objective of this study was to increase the acetate production by Clostridium thermolacticum growing on lactose, available as a renewable resource in the milk and whey permeate from the che...