河口湿地微生物群落中暗CO2固定的环境梯度评估。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-01-31 Epub Date: 2024-12-31 DOI:10.1128/aem.02177-24
Luise Grüterich, Jason Nicholas Woodhouse, Peter Mueller, Amos Tiemann, Hans-Joachim Ruscheweyh, Shinichi Sunagawa, Hans-Peter Grossart, Wolfgang R Streit
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引用次数: 0

摘要

大气中二氧化碳浓度的上升是社会关注的主要问题,因为它可能导致全球变暖。在土壤中,固定二氧化碳的微生物阻止了一些二氧化碳进入大气。然而,对暗CO2固定的控制很少进行原位研究。在这里,我们研究了河口湿地沿主要环境梯度参与微生物二氧化碳固定的关键基因的基因和转录丰度。结合元条形码、深度宏基因组和元转录组学分析的多组学方法证实,湿地微生物群拥有7种已知二氧化碳固定途径中的4种,即卡尔文循环、逆三羧酸循环、Wood-Ljungdahl途径和逆甘氨酸途径。这些通路沿几种环境梯度以高频率转录,尽管水平取决于环境生态位。值得注意的是,三羧酸反循环关键基因的转录与高硝酸盐浓度有关,而Wood-Ljungdahl途径关键基因的转录则与还原、缺氧条件有关。卡尔文循环的转录物丰度受到有机物含量高的生态位的青睐。转录本的分类鉴定表明,暗CO2固定主要与几个细菌门有关,即Desulfobacterota、Methylomirabilota、Nitrospirota、Chloroflexota和Pseudomonadota。重要性:大气中二氧化碳浓度的增加已被确定为气候变化的主要驱动因素,并对人类社会构成重大威胁。这项工作探索了土壤微生物在减缓气候变化努力中最容易被忽视的不依赖光的二氧化碳固定潜力(又称暗二氧化碳固定)。应用分子微生物工具的组合,我们的研究为二氧化碳固定途径最活跃的生态位提供了新的见解。通过确定环境因素(如氧气、盐度和有机质有效性)如何影响河口湿地环境中的这些途径,可以制定增强天然碳汇的潜在策略。我们的研究的重要性在于促进对微生物二氧化碳固定及其在全球气候系统中的潜在作用的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing environmental gradients in relation to dark CO2 fixation in estuarine wetland microbiomes.

The rising atmospheric concentration of CO2 is a major concern to society due to its global warming potential. In soils, CO2-fixing microorganisms are preventing some of the CO2 from entering the atmosphere. Yet, the controls of dark CO2 fixation are rarely studied in situ. Here, we examined the gene and transcript abundance of key genes involved in microbial CO2 fixation along major environmental gradients within estuarine wetlands. A combined multi-omics approach incorporating metabarcoding, deep metagenomic, and metatranscriptomic analyses confirmed that wetland microbiota harbor four out of seven known CO2 fixation pathways, namely, the Calvin cycle, reverse tricarboxylic acid cycle, Wood-Ljungdahl pathway, and reverse glycine pathway. These pathways are transcribed at high frequencies along several environmental gradients, albeit at different levels depending on the environmental niche. Notably, the transcription of the key genes for the reverse tricarboxylic acid cycle was associated with high nitrate concentration, while the transcription of key genes for the Wood-Ljungdahl pathway was favored by reducing, O2-poor conditions. The transcript abundance of the Calvin cycle was favored by niches high in organic matter. Taxonomic assignment of transcripts implied that dark CO2 fixation was mainly linked to a few bacterial phyla, namely, Desulfobacterota, Methylomirabilota, Nitrospirota, Chloroflexota, and Pseudomonadota.

Importance: The increasing concentration of atmospheric CO2 has been identified as the primary driver of climate change and poses a major threat to human society. This work explores the mostly overlooked potential of light-independent CO2 fixation by soil microbes (a.k.a. dark CO2 fixation) in climate change mitigation efforts. Applying a combination of molecular microbial tools, our research provides new insights into the ecological niches where CO2-fixing pathways are most active. By identifying how environmental factors, like oxygen, salinity and organic matter availability, influence these pathways in an estuarine wetland environment, potential strategies for enhancing natural carbon sinks can be developed. The importance of our research is in advancing the understanding of microbial CO2 fixation and its potential role in the global climate system.

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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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