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Optimization and Application of Fluorescence in Situ Hybridization Assay for Detecting Polyphosphate-Accumulating Microorganisms

机译:荧光原位杂交技术检测聚磷酸盐累积微生物的优化及应用

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Laboratory-scale sequencing batch reactors (SBRs) were operated on activated sludge processes were used to study enhanced biological phosphorus removal (EBPR) from wastewater. Polyphosphateaccumulating microorganisms (PAOs) play an important role during the enhanced biological phosphorus removal (EBPR) process. Fluorescence in situ hybridization (FISH) was applied to assess the proportions of microorganisms in the sludge. The aim of this study was to optimize hybridization of PAOM1X and RHC439 probes by orthogonal design. Orthogonal optimization test of the four factors were conducted under the individual three levels. The optimal hybridizition conditions were as follow: hybridization temperature 46°C, hybridization time 2.5h, washing time 15min, formamide concentration 35%(PAOMIX probe); hybridization temperature 50°C, hybridization time 2.5h, washing time 20min, formamide concentration 20% (RHC439 probe).
机译:实验室规模的分批反应器(SBR)在活性污泥工艺上运行,用于研究提高废水中生物除磷(EBPR)的能力。聚磷酸盐累积微生物(PAO)在增强的生物除磷(EBPR)过程中起着重要作用。荧光原位杂交(FISH)用于评估污泥中微生物的比例。这项研究的目的是通过正交设计优化PAOM1X和RHC439探针的杂交。在单独的三个级别下对四个因素进行正交优化测试。最佳杂交条件为:杂交温度46℃,杂交时间2.5h,洗涤时间15min,甲酰胺浓度35%(PAOMIX探针)。杂交温度50℃,杂交时间2.5h,洗涤时间20min,甲酰胺浓度20%(RHC439探针)。

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