Evidence map›Paper›PMID 30078568›Full record

ArticleCurrent biology : CB2018

A Novel Eukaryotic Denitrification Pathway in Foraminifera.

Christian Woehle, Alexandra-Sophie Roy, Nicolaas Glock, Tanita Wein, Julia Weissenbach, Philip Rosenstiel, Claas Hiebenthal, Jan Michels, Joachim Schönfeld, Tal Dagan

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
10.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 125 citations in OpenAlex.

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  16. Single crystal spectroscopy and multiple structures from one crystal (MSOX) define catalysis in copper nitrite reductases.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  17. Denitrification in foraminifera has an ancient origin and is complemented by associated bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Christian WoehleInstitute of Microbiology, Kiel University, Am Botanischen Garten 11, Kiel 24118, Germany. Electronic address: cwoehle@ifam.uni-kiel.de.
Alexandra-Sophie RoyInstitute of Microbiology, Kiel University, Am Botanischen Garten 11, Kiel 24118, Germany. Electronic address: sroy@ifam.uni-kiel.de.
Nicolaas GlockGEOMAR Helmholtz Centre for Ocean Research Kiel, Wischhofstrasse, Kiel 24148, Germany.
Tanita WeinInstitute of Microbiology, Kiel University, Am Botanischen Garten 11, Kiel 24118, Germany.
Julia WeissenbachInstitute of Microbiology, Kiel University, Am Botanischen Garten 11, Kiel 24118, Germany.
Philip RosenstielInstitute of Clinical Molecular Biology, Kiel University, Am Botanischen Garten 11, Kiel 24118, Germany.
Claas HiebenthalGEOMAR Helmholtz Centre for Ocean Research Kiel, Wischhofstrasse, Kiel 24148, Germany.
Jan MichelsInstitute of Zoology, Kiel University, Am Botanischen Garten 1-9, Kiel 24118, Germany.
Joachim SchönfeldGEOMAR Helmholtz Centre for Ocean Research Kiel, Wischhofstrasse, Kiel 24148, Germany.
Tal DaganInstitute of Microbiology, Kiel University, Am Botanischen Garten 11, Kiel 24118, Germany.
Kiel University · DEGEOMAR Helmholtz Centre for Ocean Research Kiel · DE

Funding

European Research Council 281357
6 · The paper itself

Abstract

Benthic foraminifera are unicellular eukaryotes inhabiting sediments of aquatic environments. Several species were shown to store and use nitrate for complete denitrification, a unique energy metabolism among eukaryotes. The population of benthic foraminifera reaches high densities in oxygen-depleted marine habitats, where they play a key role in the marine nitrogen cycle. However, the mechanisms of denitrification in foraminifera are still unknown, and the possibility of a contribution of associated bacteria is debated. Here, we present evidence for a novel eukaryotic denitrification pathway that is encoded in foraminiferal genomes. Large-scale genome and transcriptomes analyses reveal the presence of a denitrification pathway in foraminifera species of the genus Globobulimina. This includes the enzymes nitrite reductase (NirK) and nitric oxide reductase (Nor) as well as a wide range of nitrate transporters (Nrt). A phylogenetic reconstruction of the enzymes' evolutionary history uncovers evidence for an ancient acquisition of the foraminiferal denitrification pathway from prokaryotes. We propose a model for denitrification in foraminifera, where a common electron transport chain is used for anaerobic and aerobic respiration. The evolution of hybrid respiration in foraminifera likely contributed to their ecological success, which is well documented in palaeontological records since the Cambrian period.

Indexed as

Anion Transport ProteinsDenitrificationForaminiferaGenome, ProtozoanNitrate TransportersNitrite ReductasesOxidoreductasesPhylogenyProtozoan ProteinsAnion Transport ProteinsNitrate Transportersnitric-oxide reductaseNitrite ReductasesOxidoreductasesProtozoan Proteinsdenitrificationenergy metabolismeukaryotic evolutionforaminiferaGlobobuliminametagenomicsnitrogen cyclephylogeneticsprotiststranscriptomics

Identifiers

PMID30078568
PMCPMC6783311
OpenAlexW2885586800

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.