Ubiquitous Gammaproteobacteria dominate dark carbon fixation in coastal sediments
Marine sediments are the largest carbon sink on earth. Nearly half of dark carbon fixation in the oceans occurs in coastal sediments, but the microorganisms responsible are largely unknown. By integrating the 16S rRNA approach, single-cell genomics, metagenomics and transcriptomics with 14 C-carbon...
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Published in | The ISME Journal Vol. 10; no. 8; pp. 1939 - 1953 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.08.2016
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Marine sediments are the largest carbon sink on earth. Nearly half of dark carbon fixation in the oceans occurs in coastal sediments, but the microorganisms responsible are largely unknown. By integrating the 16S rRNA approach, single-cell genomics, metagenomics and transcriptomics with
14
C-carbon assimilation experiments, we show that uncultured
Gammaproteobacteria
account for 70–86% of dark carbon fixation in coastal sediments. First, we surveyed the bacterial 16S rRNA gene diversity of 13 tidal and sublittoral sediments across Europe and Australia to identify ubiquitous core groups of
Gammaproteobacteria
mainly affiliating with sulfur-oxidizing bacteria. These also accounted for a substantial fraction of the microbial community in anoxic, 490-cm-deep subsurface sediments. We then quantified dark carbon fixation by scintillography of specific microbial populations extracted and flow-sorted from sediments that were short-term incubated with
14
C-bicarbonate. We identified three distinct gammaproteobacterial clades covering diversity ranges on family to order level (the
Acidiferrobacter
, JTB255 and SSr clades) that made up >50% of dark carbon fixation in a tidal sediment. Consistent with these activity measurements, environmental transcripts of sulfur oxidation and carbon fixation genes mainly affiliated with those of sulfur-oxidizing
Gammaproteobacteria
. The co-localization of key genes of sulfur and hydrogen oxidation pathways and their expression in genomes of uncultured
Gammaproteobacteria
illustrates an unknown metabolic plasticity for sulfur oxidizers in marine sediments. Given their global distribution and high abundance, we propose that a stable assemblage of metabolically flexible
Gammaproteobacteria
drives important parts of marine carbon and sulfur cycles. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1751-7362 1751-7370 |
DOI: | 10.1038/ismej.2015.257 |