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分析土壤相关样品中的铁-植物络合素复合物:LC-ESI-MS/MS 与 CE-MS。

Analysis of iron-phytosiderophore complexes in soil related samples: LC-ESI-MS/MS versus CE-MS.

机构信息

Department of Chemistry, University of Natural Resources and Life Sciences, BOKU-Vienna, Vienna, Austria.

出版信息

Electrophoresis. 2012 Feb;33(4):726-33. doi: 10.1002/elps.201100466.

Abstract

Phytosiderophores (PS) form stable complexes with various transition metals. These ligands are exuded by the roots of graminacous plants as a mechanism for mobilizing and acquiring soil iron. To investigate iron mobilization and transport, a novel LC method in combination with ESI-MS/MS for the determination of three Fe(III)-complexes with mugineic acid (MA), 2'-epi-MA and 2'-deoxymugineic acid (DMA) has been developed. Liquid chromatographic separation was realized using a silica-based mixed-mode reversed phase/weak-anion exchange type stationary phase and a 50 mM ammonium acetate buffer, pH 6.5. Baseline separation of the two complex diastereomers Fe(III)-MA and Fe(III)-epi-MA could be achieved. ESI-MS/MS detection allowed for simultaneous quantification of the complexes and the free ligands. Limits of detection were determined to be 0.001 and 0.05 μM for DMA and Fe(III)-DMA, respectively. The analytical figures of merit of the novel method were evaluated and compared with a CE-ESI-MS method that we had published earlier. The LC-ESI-MS/MS method has been successfully applied to real samples derived from preliminary extraction experiments.

摘要

植物铁载体(PS)与各种过渡金属形成稳定的配合物。这些配体是禾本科植物根系分泌的一种机制,用于动员和获取土壤中的铁。为了研究铁的动员和运输,开发了一种新的 LC 方法,结合 ESI-MS/MS 用于测定三种与 mugineic 酸(MA)、2'-epi-MA 和 2'-去氧 mugineic 酸(DMA)形成的 Fe(III)-配合物。液相色谱分离是在基于硅胶的混合模式反相/弱阴离子交换型固定相和 50mM 乙酸铵缓冲液,pH6.5 条件下实现的。两种配合物非对映异构体 Fe(III)-MA 和 Fe(III)-epi-MA 可以实现基线分离。ESI-MS/MS 检测可同时定量测定配合物和游离配体。DMA 和 Fe(III)-DMA 的检测限分别为 0.001 和 0.05μM。对新方法的分析性能进行了评估,并与我们之前发表的 CE-ESI-MS 方法进行了比较。该 LC-ESI-MS/MS 方法已成功应用于初步提取实验所得的实际样品。

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