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A rapid method to quantify nitrifiers in activated sludge

机译:快速定量分析活性污泥中硝化剂的方法

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Quantification of bacteria using Fluorescence In Situ Hybridization (FISH), confocal laser scanning microscopy (CLSM) and image analysis is very time consuming and requires the availability of an expensive microscope. Therefore, a rapid method to quantify nitrifying bacteria in activated sludge using FISH and epifluorescence microscopy was developed. The quantification of the biovolume is based on manual counting of the aggregates formed by nitrifying bacteria and determination of their size. The overall uncertainty of the method was evaluated as a function of the number of analyzed microscopic fields. It was found that 10-15 microscopic fields for ammonia-oxidizing bacteria and 6-8 microscopic fields for nitrite-oxidizing bacteria per sample were optimal regarding effort and accuracy. Accordingly, the time needed for one sample was only 5-15min, compared to about 1 h for the quantification with CLSM and image analysis. As a consequence, this method also allows for the measurement of extended time series with a reasonable effort. The comparison of the determined biovolume and the measured activity showed an explicit correlation.
机译:使用荧光原位杂交(FISH),共聚焦激光扫描显微镜(CLSM)和图像分析对细菌进行定量分析非常耗时,并且需要使用昂贵的显微镜。因此,开发了一种快速的方法,用于使用FISH和落射荧光显微镜对活性污泥中的硝化细菌进行定量。生物量的定量是基于人工计数细菌硝化形成的聚集体并确定其大小。该方法的总体不确定性根据所分析的微观视野数量进行评估。结果发现,就样本的工作量和准确性而言,氨氧化细菌的10-15个微视野和亚硝酸盐氧化细菌的6-8个微视野是最佳的。因此,一个样品所需的时间仅为5-15分钟,而用CLSM进行定量和图像分析则需要约1小时。结果,该方法还允许以合理的努力来测量延长的时间序列。测定的生物量与测定的活性的比较显示出明确的相关性。

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