Ileana Pérez-Rodríguez, Stefan M. Sievert, Marilyn L. Fogel, Dionysis I. Foustoukos
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Nitrogen isotope fractionation effects from chemolithoautotrophic <math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>NO</mi>\n <mn>3</mn>\n <mo>−</mo>\n </msubsup>\n </mrow>\n </semantics></math> reduction by both microorganisms were, on the contrary, maintained under all pressure conditions. Comparable chemolithoautotrophic <math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>NO</mi>\n <mn>3</mn>\n <mo>−</mo>\n </msubsup>\n </mrow>\n </semantics></math> reducing activities between previously reported natural hydrothermal vent fluid microbial communities dominated by <i>Campylobacterota</i> at 25 MPa and <i>Campylobacterota</i> laboratory isolates at 0.2 MPa, suggest robust similarities in cell-specific <math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>NO</mi>\n <mn>3</mn>\n <mo>−</mo>\n </msubsup>\n </mrow>\n </semantics></math> reduction rates and doubling times between microbial populations and communities growing maximally under similar temperature conditions. Physiological and metabolic comparisons of our results with other studies of pressure effects on anaerobic chemolithoautotrophic processes (i.e., microbial S<sup>0</sup>-oxidation coupled to Fe(III) reduction and hydrogenotrophic methanogenesis) suggest that anaerobic chemolithoautotrophs relying on oxidation–reduction (redox) reactions that yield higher Gibbs energies experience larger shifts in cell-specific respiration rates and doubling times at increased pressures. Overall, our results advance understanding of the role of pressure, its relationship with temperature and redox conditions, and their effects on seafloor chemolithoautotrophic <math>\n <semantics>\n <mrow>\n <msubsup>\n <mi>NO</mi>\n <mn>3</mn>\n <mo>−</mo>\n </msubsup>\n </mrow>\n </semantics></math> reduction and other anaerobic chemolithoautotrophic processes.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"20 6","pages":"857-869"},"PeriodicalIF":2.7000,"publicationDate":"2022-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Physiological and metabolic responses of chemolithoautotrophic \\n \\n \\n \\n NO\\n 3\\n −\\n \\n \\n reducers to high hydrostatic pressure\",\"authors\":\"Ileana Pérez-Rodríguez, Stefan M. Sievert, Marilyn L. Fogel, Dionysis I. Foustoukos\",\"doi\":\"10.1111/gbi.12522\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>We investigated the impact of pressure on thermophilic, chemolithoautotrophic <math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>NO</mi>\\n <mn>3</mn>\\n <mo>−</mo>\\n </msubsup>\\n </mrow>\\n </semantics></math> reducing bacteria of the phyla <i>Campylobacterota</i> and <i>Aquificota</i> isolated from deep-sea hydrothermal vents. Batch incubations at 5 and 20 MPa resulted in decreased <math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>NO</mi>\\n <mn>3</mn>\\n <mo>−</mo>\\n </msubsup>\\n </mrow>\\n </semantics></math> consumption, lower cell concentrations, and overall slower growth in <i>Caminibacter mediatlanticus</i> (<i>Campylobacterota</i>) and <i>Thermovibrio ammonificans</i> (<i>Aquificota</i>), relative to batch incubations near standard pressure (0.2 MPa) conditions. Nitrogen isotope fractionation effects from chemolithoautotrophic <math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>NO</mi>\\n <mn>3</mn>\\n <mo>−</mo>\\n </msubsup>\\n </mrow>\\n </semantics></math> reduction by both microorganisms were, on the contrary, maintained under all pressure conditions. Comparable chemolithoautotrophic <math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>NO</mi>\\n <mn>3</mn>\\n <mo>−</mo>\\n </msubsup>\\n </mrow>\\n </semantics></math> reducing activities between previously reported natural hydrothermal vent fluid microbial communities dominated by <i>Campylobacterota</i> at 25 MPa and <i>Campylobacterota</i> laboratory isolates at 0.2 MPa, suggest robust similarities in cell-specific <math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>NO</mi>\\n <mn>3</mn>\\n <mo>−</mo>\\n </msubsup>\\n </mrow>\\n </semantics></math> reduction rates and doubling times between microbial populations and communities growing maximally under similar temperature conditions. Physiological and metabolic comparisons of our results with other studies of pressure effects on anaerobic chemolithoautotrophic processes (i.e., microbial S<sup>0</sup>-oxidation coupled to Fe(III) reduction and hydrogenotrophic methanogenesis) suggest that anaerobic chemolithoautotrophs relying on oxidation–reduction (redox) reactions that yield higher Gibbs energies experience larger shifts in cell-specific respiration rates and doubling times at increased pressures. Overall, our results advance understanding of the role of pressure, its relationship with temperature and redox conditions, and their effects on seafloor chemolithoautotrophic <math>\\n <semantics>\\n <mrow>\\n <msubsup>\\n <mi>NO</mi>\\n <mn>3</mn>\\n <mo>−</mo>\\n </msubsup>\\n </mrow>\\n </semantics></math> reduction and other anaerobic chemolithoautotrophic processes.</p>\",\"PeriodicalId\":173,\"journal\":{\"name\":\"Geobiology\",\"volume\":\"20 6\",\"pages\":\"857-869\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2022-09-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Geobiology\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/gbi.12522\",\"RegionNum\":2,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geobiology","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gbi.12522","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
Physiological and metabolic responses of chemolithoautotrophic
NO
3
−
reducers to high hydrostatic pressure
We investigated the impact of pressure on thermophilic, chemolithoautotrophic reducing bacteria of the phyla Campylobacterota and Aquificota isolated from deep-sea hydrothermal vents. Batch incubations at 5 and 20 MPa resulted in decreased consumption, lower cell concentrations, and overall slower growth in Caminibacter mediatlanticus (Campylobacterota) and Thermovibrio ammonificans (Aquificota), relative to batch incubations near standard pressure (0.2 MPa) conditions. Nitrogen isotope fractionation effects from chemolithoautotrophic reduction by both microorganisms were, on the contrary, maintained under all pressure conditions. Comparable chemolithoautotrophic reducing activities between previously reported natural hydrothermal vent fluid microbial communities dominated by Campylobacterota at 25 MPa and Campylobacterota laboratory isolates at 0.2 MPa, suggest robust similarities in cell-specific reduction rates and doubling times between microbial populations and communities growing maximally under similar temperature conditions. Physiological and metabolic comparisons of our results with other studies of pressure effects on anaerobic chemolithoautotrophic processes (i.e., microbial S0-oxidation coupled to Fe(III) reduction and hydrogenotrophic methanogenesis) suggest that anaerobic chemolithoautotrophs relying on oxidation–reduction (redox) reactions that yield higher Gibbs energies experience larger shifts in cell-specific respiration rates and doubling times at increased pressures. Overall, our results advance understanding of the role of pressure, its relationship with temperature and redox conditions, and their effects on seafloor chemolithoautotrophic reduction and other anaerobic chemolithoautotrophic processes.
期刊介绍:
The field of geobiology explores the relationship between life and the Earth''s physical and chemical environment. Geobiology, launched in 2003, aims to provide a natural home for geobiological research, allowing the cross-fertilization of critical ideas, and promoting cooperation and advancement in this emerging field. We also aim to provide you with a forum for the rapid publication of your results in an international journal of high standing. We are particularly interested in papers crossing disciplines and containing both geological and biological elements, emphasizing the co-evolutionary interactions between life and its physical environment over geological time.
Geobiology invites submission of high-quality articles in the following areas:
Origins and evolution of life
Co-evolution of the atmosphere, hydrosphere and biosphere
The sedimentary rock record and geobiology of critical intervals
Paleobiology and evolutionary ecology
Biogeochemistry and global elemental cycles
Microbe-mineral interactions
Biomarkers
Molecular ecology and phylogenetics.