可溶性电子梭对微生物铁还原和甲烷生成的影响。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-05-21 Epub Date: 2025-04-25 DOI:10.1128/aem.02222-24
Bhim Sen Thapa, Theodore M Flynn, Zena D Jensvold, Kenneth M Kemner, Margaret F Sladek, Edward J O'Loughlin, Christopher W Marshall
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引用次数: 0

摘要

在许多水生和陆地生态系统中,微生物对铁(Fe)的还原是生物地球化学循环和能量通量的关键部分。环境中氧化还原活性电子穿梭体的存在可能使系统发育不同的微生物群使用不溶性铁作为终端电子受体。我们研究了不同的电子穿梭对呼吸、微生物生理和微生物生态的影响。我们测试了8种不同的电子穿梭,7种醌和核黄素,氧化还原电位在0.217和-0.340 V之间。所有梭子都观察到Fe(III)的还原和乙酸的氧化。一旦Fe(III)还原开始趋于平稳,就会观察到乙酸消耗的快速增加,并且与甲烷产生的开始相吻合,除了在与航天飞机9,10-蒽醌-2-羧酸(AQC)的孵育中。铁还原速率、醋酸盐消耗速率、甲烷生成速率和微生物群落在不同穿梭体之间存在显著差异,不受氧化还原电位的影响。总的来说,与没有班车控制相比,班车似乎减少了社区的整体多样性,但某些班车是这一趋势的例外。除AQC和1,2-二羟基蒽醌(1,2- dihydroxyyanthr醌,AQZ)存在外,所有富集条件下均以地杆菌科(Geobacteraceae)为主,但每个梭菌都富集了一个独特的群落,与无梭菌对照条件有显著差异。这表明不同氧化还原活性电子梭的存在对环境中微生物生态和总碳通量有很大的影响。铁是地壳中含量第四丰富的元素,微生物对铁的还原作用是全球生物地球化学循环的重要组成部分。一个系统发育多样的微生物群能够以氧化铁作为终端电子受体来保存能量,但在铁还原环境中有利于某些分类分支的环境条件尚不清楚。在小规模富集中经常被忽视的一个复杂因素是可溶性氧化还原活性电子穿梭对铁还原速率和微生物生态的影响。我们测试了8种不同的电子穿梭对来自当地湿地的铁还原富集物的微生物生理和生态的影响。每一次电子穿梭都改变了微生物的活性,并丰富了微生物群落,这与没有电子穿梭的控制条件不同。因此,在具有许多氧化还原活性化合物的复杂地下环境中,我们提出电子穿梭是多个铁还原细菌分支共存的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of soluble electron shuttles on microbial iron reduction and methanogenesis.

In many aquatic and terrestrial ecosystems, iron (Fe) reduction by microorganisms is a key part of biogeochemical cycling and energy flux. The presence of redox-active electron shuttles in the environment potentially enables a phylogenetically diverse group of microbes to use insoluble iron as a terminal electron acceptor. We investigated the impact that different electron shuttles had on respiration, microbial physiology, and microbial ecology. We tested eight different electron shuttles, seven quinones and riboflavin, with redox potentials between 0.217 and -0.340 V. Fe(III) reduction coupled with acetate oxidation was observed with all shuttles. Once Fe(III) reduction began to plateau, a rapid increase in acetate consumption was observed and coincided with the onset of methane production, except in the incubations with the shuttle 9,10-anthraquinone-2-carboxylic acid (AQC). The rates of iron reduction, acetate consumption, methanogenesis, and the microbial communities varied significantly across the different shuttles independent of redox potential. In general, shuttles appeared to reduce the overall diversity of the community compared to no shuttle controls, but certain shuttles were exceptions to this trend. Geobacteraceae were the predominant taxonomic family in all enrichments except in the presence of AQC or 1,2-dihydroxyanthraquinone (AQZ), but each shuttle enriched a unique community significantly different from the no shuttle control conditions. This suggests that the presence of different redox-active electron shuttles can have a large influence on the microbial ecology and total carbon flux in the environment.IMPORTANCEIron is the fourth most abundant element in the Earth's crust, and the reduction of iron by microbes is an important component of global biogeochemical cycles. A phylogenetically diverse group of microbes is capable of conserving energy with oxidized iron as a terminal electron acceptor, but the environmental conditions favoring certain taxonomic clades in iron-reducing environments are unclear. One complicating factor often overlooked in small-scale enrichments is the influence of soluble, redox-active electron shuttles on the rate and microbial ecology of iron reduction. We tested the effects of eight different electron shuttles on microbial physiology and ecology in iron-reducing enrichments derived from a local wetland. Each electron shuttle varied the microbial activity and enriched for a microbial community distinct from the no shuttle control condition. Therefore, in complex subsurface environments with many redox-active compounds present, we propose electron shuttles as a reason for the coexistence of multiple clades of iron-reducing bacteria.

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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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