淡水池塘中富集的耐酸亚硝酸盐氧化硝化螺的基因组学和生理特性。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Minji Kim, Yoichi Kamagata, Soo-Je Park
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引用次数: 0

摘要

亚硝酸盐氧化细菌(NOB)在全球氮循环中起着至关重要的作用,但它们在酸性环境中的存在和适应尚不清楚。本研究揭示了一种新的耐酸NOB的培养和特性,NS4培养,隶属于硝基螺旋藻属II谱系(Nitrospira_D)。从淡水池塘沉积物中富集和分离出来的NS4培养物显示出显著的生理和基因组特征,揭示了低pH条件下NOB的生存策略。NS4文化展示了最优增长pH值6和0.5毫米亚硝酸盐浓度,最大增长率为0.62天⁻¹。动力学分析表明,它对亚硝酸盐有很高的亲和力(Km(app) = 4.02µM),表明它适应于少营养环境。系统基因组学和基因组相关性分析表明,NS4培养物是硝化螺旋菌属中的一个新成员,我们将其命名为“Candidatus Nitrospira acid toler耐受菌”。基因组研究表明存在完整的还原三羧酸循环和亚硝酸盐氧化基因,证实了其趋化岩石自养生活方式。有趣的是,NS4基因组缺乏钴胺素生物合成的完整途径,这意味着这种重要的辅因子可能依赖于共生伙伴。NS4基因组包含与耐酸相关的基因,包括伴侣蛋白、转运蛋白和氨基酸代谢,表明其具有适应或抵抗低pH条件的遗传潜力。这一发现扩大了我们对NOB多样性和适应性的理解,为酸影响生态系统中的氮循环提供了见解。这种耐酸NOB的生理和基因组特征为探索NOB在以前被忽视的酸性栖息地中的生态意义开辟了新的见解。亚硝酸盐氧化细菌(NOB)是全球氮循环不可或缺的一部分,但它们对酸性环境的适应仍然知之甚少。本研究引入了一种从淡水池塘沉积物中富集的耐酸NOB——硝基螺旋Candidatus Nitrospira。通过结合生理和基因组分析,这项工作揭示了在低pH条件下能够存活和亚硝酸盐氧化的独特适应性。值得注意的是,NS4培养物具有较高的亚硝酸盐亲和力和抗酸性胁迫能力,表明其在酸影响生态系统中的生态意义。此外,NS4基因组性状揭示了代谢依赖性的遗传潜力,包括对钴胺素合成的共生伙伴的依赖。这些发现扩大了我们对极端条件下NOB多样性及其在氮循环中的作用的理解,为微生物生态学和酸性环境中氮过程管理的潜在应用提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomics and physiological characterizations of an acidotolerant nitrite-oxidizing Nitrospira enriched from freshwater pond.

Nitrite-oxidizing bacteria (NOB) play a crucial role in global nitrogen cycling, yet their presence and adaptations in acidic environments remain poorly understood. This study unveils the cultivation and characterization of a novel acid-tolerant NOB, NS4 culture, affiliated with lineage II (Nitrospira_D) within the genus Nitrospira. Enriched and isolated from a freshwater pond sediment, NS4 culture exhibits remarkable physiological and genomic traits that shed light on NOB survival strategies in low pH conditions. NS4 culture demonstrates the optimal growth at pH 6 and 0.5 mM nitrite concentration, with a maximum growth rate of 0.62 day⁻¹. Kinetic analyses reveal a high affinity for nitrite (Km(app) = 4.02 µM), suggesting adaptation to oligotrophic environments. Phylogenomic and genomic-relatedness analyses position NS4 culture as a novel member within the genus Nitrospira, for which we propose as "Candidatus Nitrospira acidotolerans." Genomic investigations indicate the presence of a complete reductive tricarboxylic acid cycle and genes for nitrite oxidation, confirming its chemolithoautotrophic lifestyle. Intriguingly, NS4 genome lacks complete pathways for cobalamin biosynthesis, implying a potential dependence on symbiotic partners for this essential cofactor. The NS4 genome harbors genes associated with acid resistance, including chaperones, transporters, and amino acid metabolism, suggesting a genetic potential for adaptation or resistance to low pH conditions. This discovery expands our understanding of NOB diversity and adaptability, offering insights into nitrogen cycling in acid-impacted ecosystems. The physiological and genomic traits of this acid-tolerant NOB open new insights for exploring the ecological significance of NOB in previously overlooked acidic habitats.IMPORTANCENitrite-oxidizing bacteria (NOB) are integral to the global nitrogen cycle, yet their adaptations to acidic environments remain poorly understood. This study introduces Candidatus Nitrospira acidotolerans, an acid-tolerant NOB highly enriched from freshwater pond sediment. By combining physiological and genomic analyses, this work reveals unique adaptations that enable survival and nitrite oxidation under low pH conditions. Notably, the NS4 culture demonstrates high nitrite affinity and resistance to acidic stress, suggesting its ecological significance in acid-impacted ecosystems. Additionally, NS4 genomic traits reveal genetic potential of metabolic dependencies, including reliance on symbiotic partners for cobalamin synthesis. These findings expand our understanding of NOB diversity and their role in nitrogen cycling under extreme conditions, offering novel insights into microbial ecology and potential applications in managing nitrogen processes in acidic environments.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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