一种化化石自养古菌对碳限制的代谢反应。

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-30 DOI:10.1128/msystems.00732-25
Logan H Hodgskiss, Melina Kerou, Zhen-Hao Luo, Barbara Bayer, Andreas Maier, Wolfram Weckwerth, Thomas Nägele, Christa Schleper
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引用次数: 0

摘要

无处不在的氨氧化古菌从氨中产生能量,并从无机碳源中构建细胞团,从而促进全球氮和碳循环。然而,对它们预测的核心碳代谢的调控知之甚少。建立了维也纳亚硝酸菌(Nitrososphaera viennensis)的热力学模型,以估算无机碳的消耗与能量消耗的氨的关系,并通过在碳限制和过剩条件下生长的细胞进行了实验测试。对实验条件进行的蛋白质组学和代谢组学联合研究显示,无论是在过氧化氢酶还是丙酮酸作为活性氧清除剂的背景下,不同的代谢适应取决于碳供给量。蛋白质和代谢物动力学的整合揭示了碳限制下的细胞策略,以维持氨基酸池和翻译起始所需的蛋白质上调,以保持蛋白质合成的启动。建模和功能基因组学的结合填补了对化能自养、氨氧化古菌中心代谢及其调控的理解空白,即使在缺乏可用的遗传工具的情况下。氨氧化古菌(AOA)是一个广泛分布的分支,在全球氮循环中起着关键作用,同时也固定无机碳,但人们对其碳代谢的调节知之甚少。为了解决这一缺失的知识,土壤AOA亚硝基磷灰石(Nitrososphaera viennensis)受到不同水平无机碳的影响,并通过系统生物学方法进行分析,以更好地了解其核心代谢是如何调节的。结果表明,碳固定循环具有很强的依赖性,并突出了核心代谢途径之间的关键连接点。该分析还揭示了翻译过程的严格控制,并阐明了当生物体暴露于外源性过氧化氢酶或丙酮酸以减轻活性氧的氧化应激时独特的细胞反应。所呈现的数据突出了维也纳乳霉的代谢反应,并提供了更好的理解生物体以及可能的其他AOA如何响应各种环境条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic response of a chemolithoautotrophic archaeon to carbon limitation.

The ubiquitously distributed ammonia-oxidizing archaea generate energy from ammonia and build cell mass from inorganic carbon sources, thereby contributing to both the global nitrogen and carbon cycles. However, little is known about the regulation of their predicted core carbon metabolism. A thermodynamic model for Nitrososphaera viennensis was developed to estimate the consumption of inorganic carbon in relation to ammonia consumed for energy and was tested experimentally by growing cells in carbon-limited and excess conditions. A combined proteomic and metabolomic approach to the experimental conditions revealed distinct metabolic adaptation depending on the amount of carbon supplied, either in a catalase or pyruvate background as a reactive oxygen species scavenger. Integration of protein and metabolite dynamics revealed a cellular strategy under carbon limitation to maintain a pool of amino acids and an upregulation of proteins necessary for translation initiation to stay primed for protein synthesis. The combination of modeling and functional genomics fills gaps in the understanding of the central metabolism and its regulation in a chemolithoautotrophic, ammonia-oxidizing archaeon, even in the absence of available genetic tools.IMPORTANCELittle is known about the regulation of carbon metabolism within ammonia-oxidizing archaea (AOA), a widespread clade that plays a critical role in the global nitrogen cycle while also fixing inorganic carbon. To address this missing knowledge, the soil AOA Nitrososphaera viennensis was subjected to various levels of inorganic carbon and analyzed via a systems biology approach to better understand how its core metabolism is regulated. The results demonstrate a strong dependence on the carbon fixation cycle and highlight key connection points between the core metabolic pathways. The analysis additionally revealed tight control on translational processes and elucidated unique cellular responses when the organism was exposed to either exogenous catalase or pyruvate to relieve oxidative stress from reactive oxygen species. The presented data highlight metabolic responses of N. viennensis and provide a better understanding of how the organism, and likely other AOA, respond to various environmental conditions.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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