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Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide.

Publication ,  Journal Article
Islam, ZF; Cordero, PRF; Feng, J; Chen, Y-J; Bay, SK; Jirapanjawat, T; Gleadow, RM; Carere, CR; Stott, MB; Chiri, E; Greening, C
Published in: The ISME journal
July 2019

Most aerobic bacteria exist in dormant states within natural environments. In these states, they endure adverse environmental conditions such as nutrient starvation by decreasing metabolic expenditure and using alternative energy sources. In this study, we investigated the energy sources that support persistence of two aerobic thermophilic strains of the environmentally widespread but understudied phylum Chloroflexi. A transcriptome study revealed that Thermomicrobium roseum (class Chloroflexia) extensively remodels its respiratory chain upon entry into stationary phase due to nutrient limitation. Whereas primary dehydrogenases associated with heterotrophic respiration were downregulated, putative operons encoding enzymes involved in molecular hydrogen (H2), carbon monoxide (CO), and sulfur compound oxidation were significantly upregulated. Gas chromatography and microsensor experiments showed that T. roseum aerobically respires H2 and CO at a range of environmentally relevant concentrations to sub-atmospheric levels. Phylogenetic analysis suggests that the hydrogenases and carbon monoxide dehydrogenases mediating these processes are widely distributed in Chloroflexi genomes and have probably been horizontally acquired on more than one occasion. Consistently, we confirmed that the sporulating isolate Thermogemmatispora sp. T81 (class Ktedonobacteria) also oxidises atmospheric H2 and CO during persistence, though further studies are required to determine if these findings extend to mesophilic strains. This study provides axenic culture evidence that atmospheric CO supports bacterial persistence and reports the third phylum, following Actinobacteria and Acidobacteria, to be experimentally shown to mediate the biogeochemically and ecologically important process of atmospheric H2 oxidation. This adds to the growing body of evidence that atmospheric trace gases are dependable energy sources for bacterial persistence.

Duke Scholars

Published In

The ISME journal

DOI

EISSN

1751-7370

ISSN

1751-7362

Publication Date

July 2019

Volume

13

Issue

7

Start / End Page

1801 / 1813

Related Subject Headings

  • Transcriptome
  • Phylogeny
  • Oxidation-Reduction
  • Multienzyme Complexes
  • Microbiology
  • Hydrogenase
  • Hydrogen
  • Genome, Bacterial
  • Gases
  • Energy Metabolism
 

Citation

APA
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ICMJE
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Islam, Z. F., Cordero, P. R. F., Feng, J., Chen, Y.-J., Bay, S. K., Jirapanjawat, T., … Greening, C. (2019). Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide. The ISME Journal, 13(7), 1801–1813. https://doi.org/10.1038/s41396-019-0393-0
Islam, Zahra F., Paul R. F. Cordero, Joanna Feng, Ya-Jou Chen, Sean K. Bay, Thanavit Jirapanjawat, Roslyn M. Gleadow, et al. “Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide.The ISME Journal 13, no. 7 (July 2019): 1801–13. https://doi.org/10.1038/s41396-019-0393-0.
Islam ZF, Cordero PRF, Feng J, Chen Y-J, Bay SK, Jirapanjawat T, et al. Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide. The ISME journal. 2019 Jul;13(7):1801–13.
Islam, Zahra F., et al. “Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide.The ISME Journal, vol. 13, no. 7, July 2019, pp. 1801–13. Epmc, doi:10.1038/s41396-019-0393-0.
Islam ZF, Cordero PRF, Feng J, Chen Y-J, Bay SK, Jirapanjawat T, Gleadow RM, Carere CR, Stott MB, Chiri E, Greening C. Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide. The ISME journal. 2019 Jul;13(7):1801–1813.

Published In

The ISME journal

DOI

EISSN

1751-7370

ISSN

1751-7362

Publication Date

July 2019

Volume

13

Issue

7

Start / End Page

1801 / 1813

Related Subject Headings

  • Transcriptome
  • Phylogeny
  • Oxidation-Reduction
  • Multienzyme Complexes
  • Microbiology
  • Hydrogenase
  • Hydrogen
  • Genome, Bacterial
  • Gases
  • Energy Metabolism