Summary
Although metabolic pathways and associated enzymes of anaerobic ammonium oxidation (anammox) of ‘Ca. Kuenenia stuttgartiensis’ have been studied, those of other anammox bacteria are still poorly understood.
NO2− reduction to NO is considered to be the first step in the anammox metabolism of ‘Ca. K. stuttgartiensis’, however, ‘Ca. Brocadia’ lacks the genes that encode canonical NO‐forming nitrite reductases (NirS or NirK) in its genome, which is different from ‘Ca. K. stuttgartiensis’. Here, we studied the anammox metabolism of ‘Ca. Brocadia sinica’. 15N‐tracer experiments demonstrated that ‘Ca. B. sinica’ cells could reduce
NO2− to NH2OH, instead of NO, with as yet unidentified nitrite reductase(s). Furthermore, N2H4 synthesis, downstream reaction of
NO2− reduction, was investigated using a purified ‘Ca. B. sinica' hydrazine synthase (Hzs) and intact cells. Both the ‘Ca. B. sinica’ Hzs and cells utilized NH2OH and
NH4+, but not NO and
NH4+, for N2H4 synthesis and further oxidized N2H4 to N2 gas. Taken together, the metabolic pathway of ‘Ca. B. sinica’ is NH2OH‐dependent and different from the one of ‘Ca. K. stuttgartiensis’, indicating metabolic diversity of anammox bacteria.
A draft genome sequence of an anaerobic ammonium-oxidizing (anammox) bacterium, “Candidatus Brocadia sinica,” was determined by pyrosequencing and by screening a fosmid library. A 4.07-Mb genome sequence comprising 3 contigs was assembled, in which 3,912 gene-coding regions, 47 tRNAs, and a single rrn operon were annotated.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.