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Fluorometric Quantification of Natural Inorganic Polyphosphate

机译:天然无机多磷酸盐的荧光定量

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摘要

Polyphosphate, a linear polymer of orthophosphate, is abundant in the environment and a key component in wastewater treatment and many bioremediation processes. Despite the broad relevance of polyphosphate, current methods to quantify it possess significant disadvantages. Here, we describe a new approach for the direct quantification of inorganic polyphosphate in complex natural samples. The protocol relies on the interaction between the fluorochrome 4',6-diamidino-2-phenylindole (DAPI) and dissolved polyphosphate. With the DAPI-based approach we describe, polyphosphate can be quantified at concentrations ranging from 0.5-3 μM P in a neutral-buffered freshwater matrix with an accuracy of ±0.03 μM P. The patterns of polyphosphate concentration versus fluorescence yielded by standards exhibit no chain length dependence across polyphosphates ranging from 15-130 phosphorus units in size. Shorter length polyphosphate molecules (e.g., polyphosphate of three and five phosphorus units in length) contribute little to no signal in this approach, as these molecules react only slightly or not at all with DAPI in the concentration range tested. The presence of salt suppresses fluorescencefrom intermediate polyphosphate chain lengths (e.g., 15 phosphorus units) at polyphosphate concentrations ranging from 0.5-3 μM P. For longer chain lengths (e.g., 45-130 phosphorus units), this salt interference is not evident at conductivities up to ~10mS/cm. Our results indicate that standard polyphosphates should be stored frozen for no longer than 10-15 days to avoid inconsistent results associated with standard degradation. We have applied the fluorometric protocolto the analysis of five well-characterized natural samples to demonstrate the use of the method.
机译:多磷酸盐是一种正磷酸盐的线性聚合物,在环境中含量很高,是废水处理和许多生物修复过程中的关键成分。尽管多磷酸盐具有广泛的相关性,但是目前定量多磷酸盐的方法仍具有明显的缺点。在这里,我们描述了一种直接定量复杂天然样品中无机多磷酸盐的新方法。该协议依赖于荧光染料4',6-二mid基-2-苯基吲哚(DAPI)与溶解的多磷酸盐之间的相互作用。使用我们描述的基于DAPI的方法,可以在中性缓冲的淡水基质中以0.5-3μMP的浓度对多磷酸盐进行定量,精度为±0.03μMP。多磷酸盐浓度与标准品产生的荧光的关系图没有显​​示整个磷酸盐的链长依赖性介于15-130个磷单位之间。在这种方法中,较短长度的多磷酸盐分子(例如,长度为三个和五个磷单元的多磷酸盐)几乎没有信号贡献,因为这些分子在测试的浓度范围内仅与DAPI发生少许反应或根本没有反应。在多磷酸盐浓度范围为0.5-3μMP时,盐的存在抑制了来自中间多磷酸盐链长(例如15个磷单元)的荧光。对于更长的链长(例如45-130个磷单元),这种盐干扰在电导率下不明显高达〜10mS / cm。我们的结果表明标准多磷酸盐应冷冻保存不超过10-15天,以避免与标准降解相关的不一致结果。我们已将荧光分析法应用于五个特征充分的天然样品的分析,以证明该方法的使用。

著录项

  • 来源
    《Environmental Science & Technology》 |2010年第12期|P.4665-4671|共7页
  • 作者单位

    School of Earth and Atmospheric Sciences, Georgia Institute of Technology 311 Ferst Drive Atlanta Georgia 30332;

    rnSchool of Earth and Atmospheric Sciences, Georgia Institute of Technology 311 Ferst Drive Atlanta Georgia 30332;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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