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重新评估地微生物学中常用的比色铁测定方法。

Reevaluation of colorimetric iron determination methods commonly used in geomicrobiology.

机构信息

Institute of Groundwater Ecology, Helmholtz Zentrum München, German Research Center for Environmental Health, Ingolstädter Landstr. 1, D-85764 Neuherberg, Germany.

出版信息

J Microbiol Methods. 2012 Apr;89(1):41-8. doi: 10.1016/j.mimet.2012.01.021. Epub 2012 Feb 12.

Abstract

The ferrozine and phenanthroline colorimetric assays are commonly applied for the determination of ferrous and total iron concentrations in geomicrobiological studies. However, accuracy of both methods depends on slight changes in their protocols, on the investigated iron species, and on geochemical variations in sample conditions. Therefore, we tested the performance of both methods using Fe(II)((aq)), Fe(III)((aq)), mixed valence solutions, synthetic goethite, ferrihydrite, and pyrite, as well as microbially-formed magnetite and a mixture of goethite and magnetite. The results were compared to concentrations determined with aqua regia dissolution and inductively coupled plasma atomic emission spectroscopy (ICP-AES). Iron dissolution prior to the photometric assays included dissolution in 1M or 6M HCl, at 21 or 60°C, and oxic or anoxic conditions. Results indicated a good reproducibility of quantitative total iron determinations by the ferrozine and phenanthroline assays for easily soluble iron forms such as Fe(II)((aq)), Fe(III)((aq)), mixed valence solutions, and ferrihydrite. The ferrozine test underestimated total iron contents of some of these samples after dissolution in 1M HCl by 10 to 13%, whereas phenanthroline matched the results determined by ICP-AES with a deviation of 5%. Total iron concentrations after dissolution in 1M HCl of highly crystalline oxides such as magnetite, a mixture of goethite and magnetite, and goethite were underestimated by up to 95% with both methods. When dissolving these minerals in 6M HCl at 60°C, the ferrozine method was more reliable for total iron content with an accuracy of ±5%, related to values determined with ICP-AES. Phenanthroline was more reliable for the determination of total pyritic iron as well as ferrous iron after incubation in 1M HCl at 21°C in the Fe(II)((aq)) sample with a recovery of 98%. Low ferrous iron concentrations of less than 0.5mM were overestimated in a Fe(III) background by up to 150% by both methods. Heating of mineral samples in 6M HCl increased their solubility and susceptibility for both photometric assays which is a need for total iron determination of highly crystalline minerals. However, heating also rendered a subsequent reliable determination of ferrous iron impossible due to fast abiotic oxidation. Due to the low solubility of highly crystalline samples, the determination of total iron is solely possible after dissolution in 6M HCl at 60°C which on the other hand makes determination of ferrous iron impossible. The recommended procedure for ferrous iron determination is therefore incubation at 21°C in 6M HCl, centrifugation, and subsequent measurement of ferrous iron in the supernatant. The different procedures were tested during growth of G. sulfurreducens on synthetic ferrihydrite. Here, the phenanthroline test was more accurate compared to the ferrozine test. However, the latter provided easy handling and seemed preferable for larger amounts of samples.

摘要

铁嗪和邻菲啰啉比色法常用于测定地质微生物研究中的亚铁和总铁浓度。然而,两种方法的准确性取决于其方案、研究的铁物种以及样品条件的地球化学变化的微小变化。因此,我们使用 Fe(II)((aq))、Fe(III)((aq))、混合价态溶液、合成针铁矿、水铁矿和黄铁矿以及微生物形成的磁铁矿和针铁矿和磁铁矿混合物来测试这两种方法的性能。结果与用 Aqua regia 溶解和电感耦合等离子体原子发射光谱法 (ICP-AES) 确定的浓度进行了比较。在比色分析之前,铁的溶解包括在 1M 或 6M HCl 中、21°C 或 60°C 下以及有氧或缺氧条件下的溶解。结果表明,铁嗪和邻菲啰啉比色法对于容易溶解的铁形式(如 Fe(II)((aq))、Fe(III)((aq))、混合价态溶液和水铁矿)的定量总铁测定具有良好的重现性。铁嗪试验在 1M HCl 中的一些样品溶解后,总铁含量低估了 10%至 13%,而邻菲啰啉与 ICP-AES 测定结果相匹配,偏差为 5%。在 6M HCl 中于 60°C 下溶解高度结晶的氧化物(如磁铁矿、针铁矿和磁铁矿混合物以及针铁矿)后,两种方法均低估了总铁含量,最大低估幅度可达 95%。当在 21°C 下在 1M HCl 中溶解这些矿物质时,铁嗪法的总铁含量测定更为可靠,准确度为±5%,与 ICP-AES 测定值相关。对于 Fe(II)((aq))样品中孵育后测定总硫化亚铁和亚铁铁,邻菲啰啉更为可靠,回收率为 98%。在 Fe(III)背景下,两种方法都将亚铁铁的浓度低至 0.5mM 的低浓度高估了 150%。矿物样品在 6M HCl 中的加热增加了它们对两种比色法的溶解度和敏感性,这是高度结晶矿物总铁测定的需要。然而,加热也使随后可靠地测定亚铁铁变得不可能,因为亚铁铁会迅速发生非生物氧化。由于高度结晶样品的溶解度低,因此只能在 6M HCl 中于 60°C 下溶解后才能测定总铁,而另一方面又使测定亚铁铁变得不可能。因此,亚铁铁测定的推荐程序是在 6M HCl 中于 21°C 下孵育,离心,然后测定上清液中的亚铁铁。在 G. sulfurreducens 在合成水铁矿上生长期间测试了不同的程序。在此,与铁嗪法相比,邻菲啰啉法更为准确。然而,后者操作简单,对于大量样品似乎更为可取。

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