AUTHOR=Liu Qian , Chen Yuhao , Xu Xue-Wei 

TITLE=Genomic insight into strategy, interaction and evolution of nitrifiers in metabolizing key labile-dissolved organic nitrogen in different environmental niches

JOURNAL=Frontiers in Microbiology

VOLUME=14

YEAR=2023

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2023.1273211

DOI=10.3389/fmicb.2023.1273211

ISSN=1664-302X

ABSTRACT=<p>Ammonia-oxidizing archaea (AOA) and bacteria (AOB), nitrite-oxidizing bacteria (NOB), and complete ammonia oxidizers (comammox) are responsible for nitrification in nature; however, some groups have been reported to utilize labile-dissolved organic nitrogen (LDON) for satisfying nitrogen demands. To understand the universality of their capacity of LDON metabolism, we collected 70 complete genomes of AOA, AOB, NOB, and comammox from typical environments for exploring their potentials in the metabolism of representative LDON (urea, polyamines, cyanate, taurine, glycine betaine, and methylamine). Genomic analyses showed that urea was the most popular LDON used by nitrifiers. Each group harbored unique urea transporter genes (AOA: <italic>dur3</italic> and <italic>utp</italic>, AOB: <italic>utp</italic>, and NOB and comammox: <italic>urtABCDE</italic> and <italic>utp</italic>) accompanied by urease genes <italic>ureABC</italic>. The differentiation in the substrate affinity of these transporters implied the divergence of urea utilization efficiency in nitrifiers, potentially driving them into different niches. The cyanate transporter (<italic>cynABD</italic> and <italic>focA/nirC</italic>) and degradation (<italic>cynS</italic>) genes were detected mostly in NOB, indicating their preference for a wide range of nitrogen substrates to satisfy high nitrogen demands. The lack of genes involved in the metabolism of polyamines, taurine, glycine betaine, and methylamines in most of nitrifiers suggested that they were not able to serve as a source of ammonium, only if they were degraded or oxidized extracellularly as previously reported. The phylogenetic analyses assisted with comparisons of GC% and the Codon Adaptation Index between target genes and whole genomes of nitrifiers implied that urea metabolic genes <italic>dur3</italic> and <italic>ureC</italic> in AOA evolved independently from bacteria during the transition from <italic>Thaumarchaeota</italic> to AOA, while <italic>utp</italic> in terrestrial AOA was acquired from bacteria via lateral gene transfer (LGT). Cyanate transporter genes <italic>cynS</italic> and <italic>focA</italic>/<italic>nirC</italic> detected only in a terrestrial AOA <italic>Candidadus</italic> Nitrsosphaera gargensis Ga9.2 could be gained synchronously with <italic>Nitrospira</italic> of NOB by an ancient LGT. Our results indicated that LDON utilization was a common feature in nitrifiers, but metabolic potentials were different among nitrifiers, possibly being intensely interacted with their niches, survival strategies, and evolutions.</p>