反向微透析:根渗出热点的窗口

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2022-11-01 DOI:10.1016/j.soilbio.2022.108829
Alexander König , Julia Wiesenbauer , Stefan Gorka , Lilian Marchand , Barbara Kitzler , Erich Inselsbacher , Christina Kaiser
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引用次数: 3

摘要

植物根系向土壤中释放各种低分子量化合物,如糖、氨基酸或有机酸,影响其周围的微生物活动和土壤理化过程。这些化合物是土壤微生物容易获得的碳(C)和能量的来源,可能加速根系附近土壤有机质的微生物分解。然而,由于在土壤中研究这些热点的实验困难,关于根渗出热点过程的知识仍然有限。微透析是一种基于扩散的被动采样技术,已成功地用于在小空间尺度上收集土壤溶质。反向微透析,也称为反透析,可用于向土壤中引入溶质,模仿被动根渗出。然而,对物质被动扩散释放到完整土壤中的动力学知之甚少,这是应用反向微透析研究原状土壤中根系渗出热点的关键前提。在这里,我们使用反向微透析研究了13种不同的有机化合物被动引入两种不同的完整土壤的时空动态。化合物在土壤中的扩散远远低于在水中的扩散,而且不像在水中那样由分子大小决定。有趣的是,丁酸盐、草酸盐和丙酸盐进入土壤的扩散通量最高,而输入后的回取率最低,表明它们通过生物或非生物过程迅速从土壤溶液中去除。相反,葡萄糖和果糖在输入后未被清除而意外地在膜周围积聚。此外,化合物进入土壤的扩散通量表现出波动的时间模式,这可能是由于观察到添加13c标记的化合物的微生物呼吸延迟2小时。在12天的过程中,大约三分之一被引入土壤的13c标记化合物被呼吸,而8%最终进入微生物生物量。我们的研究结果表明,在完整的土壤中引入化合物会在小时的时间尺度上引发复杂的生物和非生物反应。反向微透析被证明是一种很好的工具,可以研究这种反应,以及被动释放化合物进入完整土壤的动力学和代谢后果,并与13C标记的底物和呼吸测量相结合,揭示可能由它们引发的潜在启动效应。
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Reverse microdialysis: A window into root exudation hotspots

Plant roots release a variety of low-molecular weight compounds, such as sugars, amino acids or organic acids into the soil, impacting microbial activities and physico-chemical soil processes in their surroundings. These compounds are a source of easily available Carbon (C) and energy for soil microbes, potentially accelerating microbial decomposition of soil organic matter in the immediate vicinity of roots. However, knowledge about processes in root exudation hotspots remains limited due to experimental difficulties in investigating such hotspots in soil.

Microdialysis, a passive sampling technique based on diffusion, has been successfully used to collect soil solutes at small spatial scales. Reverse microdialysis, also termed retrodialysis, can be used to introduce solutes into the soil, mimicking passive root exudation. However, little is known about the dynamics of substances released by passive diffusion into intact soil, a crucial prerequisite for applying reverse microdialysis to study root exudation hotspots in undisturbed soils.

Here, we used reverse microdialysis to investigate the spatial and temporal dynamics of thirteen different organic compounds passively introduced into two different intact soils. Diffusion of compounds into soils was substantially lower than into water, and was not – as in water – determined by molecular size. Interestingly, butyrate, oxalate and propionate showed the highest diffusive fluxes into soil combined with the lowest rate of back retrieval after input, indicating that they were quickly removed from the soil solution by biotic or abiotic processes. In contrast, glucose and fructose unexpectedly accumulated around the membrane after input without removal. Furthermore, diffusive fluxes of compounds into soils showed a fluctuating temporal pattern, which may be explained by an observed 2-h delay of microbial respiration of added 13C-labelled compounds. During the course of 12 days, approximately one third of 13C-labelled compounds introduced into soil was respired while 8% ended up in microbial biomass.

Our results demonstrate that introducing compounds into intact soil triggers complex biotic and abiotic responses at the time scale of hours. Reverse microdialysis proved to be an excellent tool to investigate such responses as well as the dynamics and metabolic consequences of passively released compounds into intact soil, and – in combination with 13C labelled substrate and respiration measurements - to shed light on potential priming effects that may be triggered by them.

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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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