Anna N. Rasmussen, Bradley B. Tolar, John R. Bargar, Kristin Boye, Christopher A. Francis
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引用次数: 0
摘要
河岸洪泛平原是包括氮元素在内的生物地球化学循环的重要区域。在这里,我们展示了来自Slate River (SR)漫滩沉积物(Crested Butte, CO, US)的硝化微生物的MAGs,包括氨氧化古菌(AOA)和comammox细菌。此外,我们还研究了硝化螺旋藻中潜在亚硝酸盐氧化细菌(NOB)的MAGs。SR地区的AOA多样性低于美国西部其他漫滩沉积物,TA-20属等亚硝化藻类谱系是主要的AOA。未回收氨氧化细菌(AOB) mag。来自Palsa-1315属(B支comammox)的微生物是SR冲积平原沉积物中最丰富的氨氧化剂。已成立的NOB明显缺席;然而,我们从NS-4家族(硝化螺)和硝化螺科的未培养谱系中恢复了mag,我们认为这是假定的NOB。根据未培养的硝化螺枝的基因组含量,亚硝酸盐氧化可能由已建立的硝化螺NOB谱系的姊妹生物进行。从SR冲积平原沉积物中回收的硝化物MAGs具有利用尿素、氰酸盐、双缩脲、三缩脲和腈等替代氨源的基因。因此,SR冲积平原似乎是一个低氨通量的环境,选择了低营养硝化菌。
Metagenome-Assembled Genomes for Oligotrophic Nitrifiers From a Mountainous Gravelbed Floodplain
Riparian floodplains are important regions for biogeochemical cycling, including nitrogen. Here, we present MAGs from nitrifying microorganisms, including ammonia-oxidising archaea (AOA) and comammox bacteria from Slate River (SR) floodplain sediments (Crested Butte, CO, US). Additionally, we explore MAGs from potential nitrite-oxidising bacteria (NOB) from the Nitrospirales. AOA diversity in SR is lower than observed in other western US floodplain sediments and Nitrosotalea-like lineages such as the genus TA-20 are the dominant AOA. No ammonia-oxidising bacteria (AOB) MAGs were recovered. Microorganisms from the Palsa-1315 genus (clade B comammox) are the most abundant ammonia-oxidizers in SR floodplain sediments. Established NOB are conspicuously absent; however, we recovered MAGs from uncultured lineages of the NS-4 family (Nitrospirales) and Nitrospiraceae that we propose as putative NOB. Nitrite oxidation may be carried out by organisms sister to established Nitrospira NOB lineages based on the genomic content of uncultured Nitrospirales clades. Nitrifier MAGs recovered from SR floodplain sediments harbour genes for using alternative sources of ammonia, such as urea, cyanate, biuret, triuret and nitriles. The SR floodplain therefore appears to be a low ammonia flux environment that selects for oligotrophic nitrifiers.
期刊介绍:
Environmental Microbiology 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