Nitrosarchaeum haohaiensis sp. Nov. CL1T: Isolation and Characterisation of a Novel Ammonia-Oxidising Archaeon From Aquatic Environments

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Hailing Li, Lingqi Zhuang, Haoyun Cai, Yimin Ni, Ting Chu, Lanming Chen, Yongxin Yu, Yongjie Wang
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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.

浙江大学学报(自然科学版);2009 - 01:一种新型氨氧化古菌的分离与鉴定
经过3.5年的富集培养,从东海洋山港分离到一株新的氨氧化古菌CL1T。菌株CL1T显示最大氨耐受性可达10 mM。其最佳生长条件为pH值7-8,盐度2%-3%,温度20℃- 25℃。在此条件下,菌株CL1T的最大特定生长速率为0.87 d−1,细胞产量估计为3.92 × 106个细胞mL−1 μM氨氮−1。基因组测序结果显示,菌株CL1T的基因组大小为1.63兆碱基,完整度高达99.95%。基于16S rRNA基因和全基因组数据的系统发育分析将菌株CL1T归入亚硝化古菌属。CL1T与近缘菌株基因组的平均核苷酸同源性(ANI)为92.01%,证实CL1T是亚硝化古菌中的一个新种。代谢途径分析表明,菌株CL1T编码氨氧化的关键酶,包括氨单加氧酶(amoA、amoB、amoC)和铜氧化酶,表明其具有氨氧化能力。此外,菌株CL1T可能通过GS-GOGAT和GDH途径同化氨。与通过电镜观察到的CL1T株细胞外囊泡(EVs)一致,基因组注释鉴定出与EVs功能相关的核心基因,如vps4和FtsZ。CL1T菌株的分离为研究其氨代谢及其与其他AOA、氨氧化细菌(AOB)和亚硝酸盐氧化细菌(NOB)的生态相互作用提供了有价值的模型系统,从而有助于深入了解水生环境中氮循环机制。
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
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.
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