首页> 外文期刊>Environmental Science & Technology >Mg Isotope Fractionation during Uptake by a Rock-Inhabiting, Model Microcolonial Fungus Knufia petricola at Acidic and Neutral pH
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Mg Isotope Fractionation during Uptake by a Rock-Inhabiting, Model Microcolonial Fungus Knufia petricola at Acidic and Neutral pH

机译:酸性和中性pH值的岩石居留型微殖民地真菌Knufia petricola在摄取过程中的镁同位素分馏

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摘要

The model rock-inhabiting microcolonial fungus Knufia petricola fractionates stable Mg isotopes in a time-and pH-dependent manner. During growth, the increase of ~(26)Mg/~(24)Mg in the fungal cells relative to the growth media amounted to 0.65 ± 0.14‰ at pH 6 and 1.11 ± 0.35‰ at pH 3. We suggest a constant equilibrium fractionation factor during incorporation of Mg into ribosomes and ATP as a cause of enrichment of ~(26)Mg in the cells. We suggest too that the proton gradient across the cell wall and cytoplasmic membrane controls Mg~(2+) transport into the fungal cell. As the strength of this gradient is a function of extracellular solution pH, the pH-dependence on Mg isotope fractionation is thus due to differences in fungal cell mass fluxes. Through a mass balance model we show that Mg uptake into the fungal cell is not associated with a unique Mg isotope fractionation factor. This Mg isotope fractionation dependence on pH might also be observed in any organism with cells that follow similar Mg uptake and metabolic pathways and serves to reveal Mg cycling in ecosystems.
机译:居住在岩石中的模型微殖民地真菌小桐子(Knufia petricola)以时间和pH依赖的方式分离稳定的Mg同位素。在生长过程中,相对于生长培养基,真菌细胞中〜(26)Mg /〜(24)Mg的增加在pH 6时为0.65±0.14‰,在pH 3时为1.11±0.35‰。我们建议进行恒定的平衡分离Mg掺入核糖体和ATP的过程中的“α”因子是细胞中〜(26)Mg富集的原因。我们也建议跨细胞壁和细胞质膜的质子梯度控制Mg〜(2+)转运到真菌细胞中。由于该梯度的强度是细胞外溶液pH的函数,因此pH对Mg同位素分馏的依赖性是由于真菌细胞质量通量的差异所致。通过质量平衡模型,我们表明,镁向真菌细胞的吸收与唯一的镁同位素分级因子无关。在任何具有遵循相似的Mg吸收和代谢途径的细胞的生物中,也可能观察到这种Mg同位素对pH的分级依赖性,并有助于揭示Mg在生态系统中的循环。

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  • 来源
    《Environmental Science & Technology》 |2017年第17期|9691-9699|共9页
  • 作者单位

    Section 3.3, Earth Surface Geochemistry, GFZ German Research Centre for Geosciences, Telegrafenberg, 14473 Potsdam, Germany,Institute of Geological Sciences, Freie Universitat Berlin, 12249 Berlin, Germany;

    Department 4, Materials & Environment, BAM Federal Institute for Materials Research & Testing, 12205 Berlin, Germany,Department of Biology, Chemistry, and Pharmacy, Freie Universitat Berlin, 14195 Berlin, Germany;

    Section 3.3, Earth Surface Geochemistry, GFZ German Research Centre for Geosciences, Telegrafenberg, 14473 Potsdam, Germany;

    Section 3.3, Earth Surface Geochemistry, GFZ German Research Centre for Geosciences, Telegrafenberg, 14473 Potsdam, Germany,Department 4, Materials & Environment, BAM Federal Institute for Materials Research & Testing, 12205 Berlin, Germany;

    Institute of Geological Sciences, Freie Universitat Berlin, 12249 Berlin, Germany,Department 4, Materials & Environment, BAM Federal Institute for Materials Research & Testing, 12205 Berlin, Germany,Department of Biology, Chemistry, and Pharmacy, Freie Universitat Berlin, 14195 Berlin, Germany;

    Section 3.3, Earth Surface Geochemistry, GFZ German Research Centre for Geosciences, Telegrafenberg, 14473 Potsdam, Germany,Institute of Geological Sciences, Freie Universitat Berlin, 12249 Berlin, Germany;

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  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-17 13:57:49

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