{"title":"Nitrosarchaeum haohaiensis sp. Nov. CL1T: Isolation and Characterisation of a Novel Ammonia-Oxidising Archaeon From Aquatic Environments","authors":"Hailing Li, Lingqi Zhuang, Haoyun Cai, Yimin Ni, Ting Chu, Lanming Chen, Yongxin Yu, Yongjie Wang","doi":"10.1111/1758-2229.70100","DOIUrl":null,"url":null,"abstract":"<p>Following a 3.5-year enrichment cultivation period, a novel ammonia-oxidising archaeon (AOA), designated strain CL1<sup>T</sup>, was isolated from Yangshan Harbour (East China Sea). Strain CL1<sup>T</sup> demonstrates a maximum ammonia tolerance of up to 10 mM. Its optimal growth conditions include a pH range of 7–8, a salinity of 2%–3%, and a temperature range of 20°C–25°C. Under these conditions, strain CL1<sup>T</sup> achieved a maximum specific growth rate of 0.87 d<sup>−1</sup>, with cell yields estimated at 3.92 × 10<sup>6</sup> cells mL<sup>−1</sup> μM ammonia<sup>−1</sup>. Genomic sequencing revealed that strain CL1<sup>T</sup> possesses a genome size of 1.63 megabases with a high completeness of 99.95%. Phylogenetic analysis based on the 16S rRNA gene and whole-genome data placed strain CL1<sup>T</sup> within the genus <i>Nitrosarchaeum</i>. The average nucleotide identity (ANI) between the genome of strain CL1<sup>T</sup> and its closest relative was 92.01%, confirming that strain CL1<sup>T</sup> represents a novel species within <i>Nitrosarchaeum</i>. Metabolic pathway analysis demonstrated that strain CL1<sup>T</sup> encodes key enzymes for ammonia oxidation, including ammonia monooxygenase (<i>amoA</i>, <i>amoB</i>, <i>amoC</i>) and copper oxidase, indicating its capacity for ammonia oxidation. Additionally, strain CL1<sup>T</sup> likely assimilates ammonia through the GS-GOGAT and GDH pathways. Consistent with the observation of extracellular vesicles (EVs) in strain CL1<sup>T</sup> via electron microscopy, genome annotation identified core genes associated with EVs function, such as <i>vps4</i> and <i>FtsZ</i>. The isolation of strain CL1<sup>T</sup> provides a valuable model system for investigating its ammonia metabolism and exploring its ecological interactions with other AOA, ammonia-oxidising bacteria (AOB) and nitrite-oxidising bacteria (NOB), thereby contributing to a deeper understanding of nitrogen cycling mechanisms in aquatic environments.</p>","PeriodicalId":163,"journal":{"name":"Environmental Microbiology Reports","volume":"17 3","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1758-2229.70100","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Microbiology Reports","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1758-2229.70100","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Following a 3.5-year enrichment cultivation period, a novel ammonia-oxidising archaeon (AOA), designated strain CL1T, was isolated from Yangshan Harbour (East China Sea). Strain CL1T demonstrates a maximum ammonia tolerance of up to 10 mM. Its optimal growth conditions include a pH range of 7–8, a salinity of 2%–3%, and a temperature range of 20°C–25°C. Under these conditions, strain CL1T achieved a maximum specific growth rate of 0.87 d−1, with cell yields estimated at 3.92 × 106 cells mL−1 μM ammonia−1. Genomic sequencing revealed that strain CL1T possesses a genome size of 1.63 megabases with a high completeness of 99.95%. Phylogenetic analysis based on the 16S rRNA gene and whole-genome data placed strain CL1T within the genus Nitrosarchaeum. The average nucleotide identity (ANI) between the genome of strain CL1T and its closest relative was 92.01%, confirming that strain CL1T represents a novel species within Nitrosarchaeum. Metabolic pathway analysis demonstrated that strain CL1T encodes key enzymes for ammonia oxidation, including ammonia monooxygenase (amoA, amoB, amoC) and copper oxidase, indicating its capacity for ammonia oxidation. Additionally, strain CL1T likely assimilates ammonia through the GS-GOGAT and GDH pathways. Consistent with the observation of extracellular vesicles (EVs) in strain CL1T via electron microscopy, genome annotation identified core genes associated with EVs function, such as vps4 and FtsZ. The isolation of strain CL1T provides a valuable model system for investigating its ammonia metabolism and exploring its ecological interactions with other AOA, ammonia-oxidising bacteria (AOB) and nitrite-oxidising bacteria (NOB), thereby contributing to a deeper understanding of nitrogen cycling mechanisms in aquatic environments.
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.