Physiological and metabolic responses of chemolithoautotrophic NO 3 − reducers to high hydrostatic pressure

IF 2.7 2区 地球科学 Q2 BIOLOGY
Geobiology Pub Date : 2022-09-08 DOI:10.1111/gbi.12522
Ileana Pérez-Rodríguez, Stefan M. Sievert, Marilyn L. Fogel, Dionysis I. Foustoukos
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引用次数: 0

Abstract

We investigated the impact of pressure on thermophilic, chemolithoautotrophic NO 3 reducing bacteria of the phyla Campylobacterota and Aquificota isolated from deep-sea hydrothermal vents. Batch incubations at 5 and 20 MPa resulted in decreased NO 3 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 NO 3 reduction by both microorganisms were, on the contrary, maintained under all pressure conditions. Comparable chemolithoautotrophic NO 3 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 NO 3 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 NO 3 reduction and other anaerobic chemolithoautotrophic processes.

化学岩石自养NO 3−还原剂对高静水压力的生理和代谢反应
我们研究了压力对深海热液喷口分离的弯曲菌门和水蛭门的嗜热、化能自养NO 3−还原细菌的影响。与标准压力(0.2 MPa)条件下的分批培养相比,在5和20 MPa条件下的分批培养导致中大西洋Caminibacter mediatlanticus (Campylobacterota)和Thermovibrio amificans (Aquificota)的NO 3−消耗减少,细胞浓度降低,总体生长速度减慢。相反,在所有压力条件下,这两种微生物的化化岩石自养NO 3−还原的氮同位素分馏效应都保持不变。先前报道的以弯曲菌群为主的天然热液喷口流体微生物群落在25 MPa和在0.2 MPa下弯曲菌群实验室分离物的化学岩石自养NO 3−还原活性比较结果表明,在相似温度条件下,微生物种群和微生物群落在细胞特异性NO 3−还原速率和倍增率方面具有很强的相似性。将我们的研究结果与其他关于压力对厌氧化石化自养过程影响的研究(即微生物氧化与铁(III)还原和氢营养化甲烷生成)的生理和代谢比较表明,依靠氧化还原(氧化还原)反应产生更高吉布斯能量的厌氧化石化自养生物在细胞特异性呼吸速率方面经历了更大的变化,并且在压力增加时增加了一倍。总的来说,我们的研究结果促进了对压力的作用、压力与温度和氧化还原条件的关系,以及它们对海底化学化石自养no3−还原和其他厌氧化学化石自养过程的影响的理解。
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来源期刊
Geobiology
Geobiology 生物-地球科学综合
CiteScore
6.80
自引率
5.40%
发文量
56
审稿时长
3 months
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.
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