Luise Grüterich, Jason Nicholas Woodhouse, Peter Mueller, Amos Tiemann, Hans-Joachim Ruscheweyh, Shinichi Sunagawa, Hans-Peter Grossart, Wolfgang R Streit
{"title":"河口湿地微生物群落中暗CO2固定的环境梯度评估。","authors":"Luise Grüterich, Jason Nicholas Woodhouse, Peter Mueller, Amos Tiemann, Hans-Joachim Ruscheweyh, Shinichi Sunagawa, Hans-Peter Grossart, Wolfgang R Streit","doi":"10.1128/aem.02177-24","DOIUrl":null,"url":null,"abstract":"<p><p>The rising atmospheric concentration of CO<sub>2</sub> is a major concern to society due to its global warming potential. In soils, CO<sub>2</sub>-fixing microorganisms are preventing some of the CO<sub>2</sub> from entering the atmosphere. Yet, the controls of dark CO<sub>2</sub> fixation are rarely studied <i>in situ</i>. Here, we examined the gene and transcript abundance of key genes involved in microbial CO<sub>2</sub> 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 CO<sub>2</sub> 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, O<sub>2</sub>-poor conditions. The transcript abundance of the Calvin cycle was favored by niches high in organic matter. Taxonomic assignment of transcripts implied that dark CO<sub>2</sub> fixation was mainly linked to a few bacterial phyla, namely, <i>Desulfobacterota</i>, <i>Methylomirabilota</i>, <i>Nitrospirota</i>, <i>Chloroflexota</i>, and <i>Pseudomonadota</i>.</p><p><strong>Importance: </strong>The increasing concentration of atmospheric CO<sub>2</sub> 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 CO<sub>2</sub> fixation by soil microbes (a.k.a. dark CO<sub>2</sub> fixation) in climate change mitigation efforts. Applying a combination of molecular microbial tools, our research provides new insights into the ecological niches where CO<sub>2</sub>-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 CO<sub>2</sub> fixation and its potential role in the global climate system.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0217724"},"PeriodicalIF":3.9000,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11784365/pdf/","citationCount":"0","resultStr":"{\"title\":\"Assessing environmental gradients in relation to dark CO<sub>2</sub> fixation in estuarine wetland microbiomes.\",\"authors\":\"Luise Grüterich, Jason Nicholas Woodhouse, Peter Mueller, Amos Tiemann, Hans-Joachim Ruscheweyh, Shinichi Sunagawa, Hans-Peter Grossart, Wolfgang R Streit\",\"doi\":\"10.1128/aem.02177-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The rising atmospheric concentration of CO<sub>2</sub> is a major concern to society due to its global warming potential. In soils, CO<sub>2</sub>-fixing microorganisms are preventing some of the CO<sub>2</sub> from entering the atmosphere. Yet, the controls of dark CO<sub>2</sub> fixation are rarely studied <i>in situ</i>. Here, we examined the gene and transcript abundance of key genes involved in microbial CO<sub>2</sub> 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 CO<sub>2</sub> 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, O<sub>2</sub>-poor conditions. The transcript abundance of the Calvin cycle was favored by niches high in organic matter. Taxonomic assignment of transcripts implied that dark CO<sub>2</sub> fixation was mainly linked to a few bacterial phyla, namely, <i>Desulfobacterota</i>, <i>Methylomirabilota</i>, <i>Nitrospirota</i>, <i>Chloroflexota</i>, and <i>Pseudomonadota</i>.</p><p><strong>Importance: </strong>The increasing concentration of atmospheric CO<sub>2</sub> 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 CO<sub>2</sub> fixation by soil microbes (a.k.a. dark CO<sub>2</sub> fixation) in climate change mitigation efforts. Applying a combination of molecular microbial tools, our research provides new insights into the ecological niches where CO<sub>2</sub>-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. 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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.
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.