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The physiological potential of anammox bacteria as revealed by their core genome structure.

Authors :
Okubo T
Toyoda A
Fukuhara K
Uchiyama I
Harigaya Y
Kuroiwa M
Suzuki T
Murakami Y
Suwa Y
Takami H
Source :
DNA research : an international journal for rapid publication of reports on genes and genomes [DNA Res] 2021 Jan 19; Vol. 28 (1).
Publication Year :
2021

Abstract

We present here the second complete genome of anaerobic ammonium oxidation (anammox) bacterium, Candidatus (Ca.) Brocadia pituitae, along with those of a nitrite oxidizer and two incomplete denitrifiers from the anammox bacterial community (ABC) metagenome. Although NO2- reduction to NO is considered to be the first step in anammox, Ca. B. pituitae lacks nitrite reductase genes (nirK and nirS) responsible for this reaction. Comparative genomics of Ca. B. pituitae with Ca. Kuenenia stuttgartiensis and six other anammox bacteria with nearly complete genomes revealed that their core genome structure contains 1,152 syntenic orthologues. But nitrite reductase genes were absent from the core, whereas two other Brocadia species possess nirK and these genes were horizontally acquired from multiple lineages. In contrast, at least five paralogous hydroxylamine oxidoreductase genes containing candidate ones (hao2 and hao3) encoding another nitrite reductase were observed in the core. Indeed, these two genes were also significantly expressed in Ca. B. pituitae as in other anammox bacteria. Because many nirS and nirK genes have been detected in the ABC metagenome, Ca. B. pituitae presumably utilises not only NO supplied by the ABC members but also NO and/or NH2OH by self-production for anammox metabolism.<br /> (© The Author(s) 2020. Published by Oxford University Press on behalf of Kazusa DNA Research Institute.)

Details

Language :
English
ISSN :
1756-1663
Volume :
28
Issue :
1
Database :
MEDLINE
Journal :
DNA research : an international journal for rapid publication of reports on genes and genomes
Publication Type :
Academic Journal
Accession number :
33367889
Full Text :
https://doi.org/10.1093/dnares/dsaa028