Obtaining complete and canonical ammonia-oxidizing bacteria through specific labeling and cell sorting.

IF 5.1 Q1 ECOLOGY
ISME communications Pub Date : 2025-02-08 eCollection Date: 2025-01-01 DOI:10.1093/ismeco/ycae145
Pieter Blom, Pascal C Huizing, João P R C de Monlevad, Maartje A H J van Kessel, Sebastian Lücker
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Abstract

Mitigation of the negative environmental consequences of excess anthropogenic nitrogen input requires a thorough understanding of the processes driving the biogeochemical nitrogen cycle. Nitrification is one of the key nitrogen-cycling processes and is performed by ammonia-oxidizing bacteria and archaea, nitrite-oxidizing bacteria, and complete nitrifiers. However, the fastidious growth of nitrifiers largely hampered their isolation using classical cultivation techniques, as most nitrifiers do not grow on solid media. Here, we present a workflow for the targeted enrichment and isolation of complete and canonical ammonia-oxidizing bacteria by combining function-specific in vivo fluorescent labeling with cell sorting. Optimized floc disruption and labeling techniques enlarged the fraction of planktonic cells and the fluorescent signal intensity, respectively, while maintaining cell viability. Sorted fractions were incubated in ammonium-containing mineral media and were screened for nitrite and nitrate production. Nitrifying cultures were upscaled and characterized with 16S ribosomal ribonucleic acid and amoA gene-targeted polymerase chain reactions and fluorescence in situ hybridization. Overall, we obtained one axenic and one enriched Nitrosomonas, and seven comammox Nitrospira enrichment cultures from five bioreactors, a recirculating aquaculture system biofilter, and agricultural soil. In conclusion, the presented workflow enables the fast and targeted retrieval of ammonia oxidizers from complex samples, allowing for in-depth physiological characterization.

通过特异性标记和细胞分选,获得完整、规范的氨氧化细菌。
要减轻过量人为氮输入对环境造成的负面影响,就必须彻底了解驱动生物地球化学氮循环的过程。硝化作用是关键的氮循环过程之一,由氨氧化细菌和古细菌、亚硝酸盐氧化细菌和完全硝化菌完成。然而,由于大多数硝化菌不能在固体培养基上生长,传统的培养技术在很大程度上阻碍了硝化菌的生长。在这里,我们提出了一种结合功能特异性体内荧光标记和细胞分选的工作流程,用于靶向富集和分离完整和典型的氨氧化细菌。优化的絮团破坏和标记技术分别提高了浮游细胞的比例和荧光信号强度,同时保持了细胞的活力。分选后的馏分在含铵矿物培养基中孵育,筛选生产亚硝酸盐和硝酸盐。采用16S核糖体核糖核酸和amoA基因靶向聚合酶链反应和荧光原位杂交技术对硝化培养物进行了扩增和鉴定。总体而言,我们从5个生物反应器、循环水养殖系统生物过滤器和农业土壤中获得了1个无菌和1个富集亚硝化单胞菌,以及7个共生硝化单胞菌富集培养物。总之,所提出的工作流程能够从复杂样品中快速和有针对性地检索氨氧化剂,从而进行深入的生理表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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