Biological Sciences Division, Earth and Biological Sciences Directorate, Pacific Northwest National Laboratorygrid.451303.0, Richland, Washington, USA.
Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratorygrid.451303.0, Richland, Washington, USA.
Appl Environ Microbiol. 2022 Jun 28;88(12):e0050522. doi: 10.1128/aem.00505-22. Epub 2022 Jun 2.
Soil nitrogen (N) transformations constrain terrestrial net primary productivity and are driven by the activity of soil microorganisms. Free-living N fixation (FLNF) is an important soil N transformation and key N input to terrestrial systems, but the forms of N contributed to soil by FLNF are poorly understood. To address this knowledge gap, a focus on microorganisms and microbial scale processes is needed that links N-fixing bacteria and their contributed N sources to FLNF process rates. However, studying the activity of soil microorganisms poses inherent challenges, including differences in sampling scale between microorganism and process rates, which can be addressed with culture-based studies and an emphasis on microbial-scale measurements. Culture conditions can differ significantly from soil conditions, so it also important that such studies include multiple culture conditions like liquid and solid media as proxies for soil environments like soil pore water and soil aggregate surfaces. Here we characterized extracellular N-containing metabolites produced by two common, diazotrophic soil bacteria in liquid and solid media, with or without N, across two sampling scales (bulk via GC-MS and spatially resolved via MALDI mass spec imaging). We found extracellular production of inorganic and organic N during FLNF, indicating terrestrial N contributions from FLNF occur in multiple forms not only as ammonium as previously thought. Extracellular metabolite profiles differed between liquid and solid media supporting previous work indicating environmental structure influences microbial function. Metabolite profiles also differed between sampling scales underscoring the need to quantify microbial scale conditions to accurately interpret microbial function. Free-living nitrogen-fixing bacteria contribute significantly to terrestrial nitrogen availability; however, the forms of nitrogen contributed by this process are poorly understood. This is in part because of inherent challenges to studying soil microorganisms , such as vast differences in scale between microorganism and ecosystem and complexities of the soil system (e.g., opacity, chemical complexity). Thus, upscaling important ecosystem processes driven by soil microorganisms, like free-living nitrogen fixation, requires microbial-scale measurements in controlled systems. Our work generated bulk and spatially resolved measurements of nitrogen released during free-living nitrogen fixation under two contrasting growth conditions analogous to soil pores and aggregates. This work allowed us to determine that diverse forms of nitrogen are likely contributed to terrestrial systems by free-living nitrogen bacteria. We also demonstrated that microbial habitat (e.g., liquid versus solid media) alters microbial activity and that measurement of microbial activity is altered by sampling scale (e.g., bulk versus spatially resolved) highlighting the critical importance of quantifying microbial-scale processes to upscaling of ecosystem function.
土壤氮(N)转化制约着陆地净初级生产力,而土壤微生物的活动则驱动着这一过程。自生固氮(FLNF)是一种重要的土壤 N 转化过程,也是陆地系统中重要的 N 输入源,但 FLNF 为土壤贡献的 N 形式还不甚了解。为了解决这一知识空白,需要关注微生物及其微生物尺度过程,将固氮细菌及其贡献的 N 源与 FLNF 过程速率联系起来。然而,研究土壤微生物的活性存在固有挑战,包括微生物和过程速率之间采样尺度的差异,这可以通过培养研究和强调微生物尺度的测量来解决。培养条件与土壤条件可能有很大差异,因此,此类研究还应包括多种培养条件,如液体和固体培养基,以作为土壤环境(如土壤孔隙水和土壤团聚体表面)的替代物。在这里,我们在两个采样尺度(通过气相色谱-质谱法进行的批量分析和通过 MALDI 质谱成像进行的空间分辨分析)下,描述了两种常见的、具有固氮能力的土壤细菌在液体和固体培养基中有无 N 条件下产生的细胞外含 N 代谢产物。我们发现 FLNF 过程中会产生无机和有机 N 的细胞外产生,表明 FLNF 从陆地贡献的 N 以多种形式存在,不仅如先前认为的那样仅为铵态。液体和固体培养基之间的细胞外代谢产物谱不同,这支持了先前的工作,即环境结构会影响微生物功能。代谢产物谱在采样尺度之间也存在差异,这强调了需要量化微生物尺度条件才能准确解释微生物功能。自生固氮细菌对陆地氮的可利用性有重要贡献;然而,这一过程贡献的氮形式还不甚了解。这在一定程度上是由于研究土壤微生物存在固有挑战,例如微生物和生态系统之间的尺度差异巨大,以及土壤系统的复杂性(例如不透明性、化学复杂性)。因此,要扩大土壤微生物驱动的重要生态系统过程(如自生固氮),需要在受控系统中进行微生物尺度的测量。我们的工作在两种对比生长条件下生成了游离生活固氮过程中释放的氮的批量和空间分辨测量结果,这两种条件类似于土壤孔隙和团聚体。这使我们能够确定,自生固氮细菌可能会以多种形式为陆地系统贡献氮。我们还表明,微生物生境(例如液体与固体培养基)会改变微生物的活性,而采样尺度(例如批量与空间分辨)会改变微生物活性的测量,这突出了量化微生物尺度过程对生态系统功能扩大的至关重要性。