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Assessing the correlation between anaerobic toluene degradation activity and bssA concentrations in hydrocarbon-contaminated aquifer material

机译:评估厌氧甲苯降解活性与受烃污染的含水层材料中bssA浓度之间的相关性

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摘要

The assessment of biodegradation activity in contaminated aquifers is critical to demonstrate the performance of bioremediation and natural attenuation and to parameterize models of contaminant plume dynamics. Real time quantitative PCR (qPCR) was used to target the catabolic bssA gene (coding for benzylsuccinate synthase) and a 16S rDNA phylogenetic gene (for total Bacteria) as potential biomarkers to infer on anaerobic toluene degradation rates. A significant correlation (P = 0.0003) was found over a wide range of initial toluene concentrations (1-100 mg/l) between toluene degradation rates and bssA concentrations in anaerobic microcosms prepared with aquifer material from a hydrocarbon contaminated site. In contrast, the correlation between toluene degradation activity and total Bacteria concentrations was not significant (P = 0.1125). This suggests that qPCR targeting of functional genes might offer a simple approach to estimate in situ biodegradation activity, which would enhance site investigation and modeling of natural attenuation at hydrocarbon-contaminated sites.
机译:对受污染含水层中生物降解活性的评估对于证明生物修复和自然衰减的性能以及对污染物羽流动力学模型进行参数化至关重要。实时定量PCR(qPCR)用于靶向分解代谢的bssA基因(编码丁二酸琥珀酸合酶)和16S rDNA系统发育基因(用于总细菌)作为推断厌氧甲苯降解速率的潜在生物标记。在由烃污染地点的含水层材料制备的厌氧微观世界中,甲苯降解速率与bssA浓度之间的广泛范围内,甲苯降解率和bssA浓度之间存在很大的相关性(P = 0.0003)。相反,甲苯降解活性与总细菌浓度之间的相关性不显着(P = 0.1125)。这表明靶向功能基因的qPCR可能提供一种简单的方法来评估原位生物降解活性,这将加强现场调查和对烃污染现场自然衰减的建模。

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