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Microdialysis as an in situ technique for sampling soil enzymes

机译:MicrodiaLysis作为用于抽样土壤酶的原位技术

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Soil extracellular enzyme activity (EEA) represents a critical bottleneck in the release of bioavailable nutrients from organic materials. However, quantifying spatial and temporal dynamics of EEA remains challenging. Techniques which measure the activity of, or directly sample free enzymes in situ may assist in understanding the short-term exoproteomic responses of microbes and roots to substrates, but few tools exist to explore EEA with minimal disturbance. We explore the potential of in situ microdialysis to directly sample soil enzymes, measuring their activity using a modified enzyme assay. We hypothesise that the technique's bias towards free solutes will also allow differentiation of free and stabilised enzyme pools. As little is known about the efficiency of micro dialysis to sample enzymes from soil, recovery of a protease standard was quantified from solution and soil, finding that enzyme recovery is hindered at lower soil moisture contents. We further measured the response of native protease activity after the addition of soybean litter to clay and sandy soils, finding microdialysis observed greater EEA in litter-amended treatments than controls in both soil types. In comparison, EEA as measured by conventional extraction-incubation methods was only greater in amended clay soils. In a final experiment, hydrolytic enzyme activity of free and stabilised clay soil fractions were estimated using microdialysis. Free enzymes contributed 9% of total hydrolytic activity in soil without litter, increasing to 46% in litter-amended soil, suggesting fresh litter promoted a transient increase in the production of free exoenzymes by soil microbes. In contrast, the addition of litter had no significant effect on stabilised EEA. In spite of the obvious challenges involved in applying microdialysis as a method for soil protein sampling, this method offers new possibilities for investigating challenging spatial and temporal aspects of enzyme dynamics and protein availability in soils.
机译:土壤细胞外酶活性(EEA)代表了来自有机材料的生物可利用营养素的临界瓶颈。然而,量化EEA的空间和时间动态仍然具有挑战性。测量原位的措施或直接样品自由酶的技术可以有助于理解微生物和根部的短期外蛋白应答,但存在很少的工具来探索截止的扰动。我们探讨原位微生物的潜力直接样品土壤酶,使用改性酶测定测量它们的活性。我们假设该技术对自由溶质的偏见也将允许分化自由和稳定的酶库。关于从土壤中的微透析的效率熟知的微透析效率,从溶液和土壤中量化蛋白酶标准的回收,发现在较低土壤水分含量下阻碍酶回收。我们进一步测量了在加入大豆凋落物到粘土和砂土后的天然蛋白酶活性的响应,发现微透过于凋落物修正的治疗中观察到更大的EEA,而不是两种土壤类型的对照。相比之下,通过常规提取 - 孵育方法测量的EEA在修正的粘土污垢中仅更大。在最后的实验中,使用微透析估计自由和稳定的粘土土壤级分的水解酶活性。自由酶在没有垃圾的情况下导致土壤中水解活性的9%,凋落物修正的土壤中增加至46%,提出新鲜的垃圾促进了土壤微生物生产自由脱酶的瞬态增加。相比之下,添加凋落物对稳定的EEA没有显着影响。尽管将微透析性施用作为土壤蛋白质采样方法的方法,但这种方法提供了一种研究酶动态和蛋白质可用性在土壤中的挑战性空间和时间方面的新可能性。

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