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历史污染地下水中厌氧烃降解的双重生物标志物。

Dual biomarkers of anaerobic hydrocarbon degradation in historically contaminated groundwater.

机构信息

Department of Environmental Sciences, School of Environmental and Biological Sciences, Rutgers, The State University of New Jersey , New Brunswick, New Jersey 08901, United States.

出版信息

Environ Sci Technol. 2011 Apr 15;45(8):3407-14. doi: 10.1021/es103859t. Epub 2011 Mar 25.

Abstract

This study reports that ongoing in situ anaerobic hydrocarbon biodegradation at a manufactured gas plant impacted site is occurring, 9 years after the initial investigation. Groundwater samples from the site monitoring wells (MW) were analyzed for biomarkers by GC-MS, end-point PCR, and quantitative PCR (qPCR). Metabolic biomarkers included specific intermediates of anaerobic naphthalene and/or 2-methylnaphthalene degradation: 2-naphthoic acid (2-NA); 5,6,7,8-tetrahydro-2-NA (TH-2-NA); hexahydro-2-NA (HH-2-NA); and carboxylated-2-methylnaphthalene (MNA). The analogues of gene bssA, encoding alpha subunit of enzyme benzylsuccinate synthase, were used as a genetic biomarker. Results indicate 1-2 orders of magnitude higher abundance of total bacteria in the impacted wells than in the unimpacted wells. End-point PCR analysis of bssA gene, with degenerate primers, indicated the presence of hydrocarbon degrading bacteria within the plume. In qPCR analysis, using primers based on toluene-degrading denitrifying or sulfate-reducing/methanogenic bacteria, bssA genes were detected only in MW-24, located downstream from the source. Metabolic biomarkers were detected in multiple wells. The highest abundance of 2-NA (6.7 μg/L), TH-2-NA (2.6 μg/L), HH-2-NA, and MNA was also detected in MW-24. The distribution of two independent biomarkers indicates that the site is enriched for anaerobic hydrocarbon biodegradation and provides strong evidence in support of natural attenuation.

摘要

本研究报告称,在最初调查 9 年后,一家煤气厂污染场地仍在进行原位厌氧烃生物降解。对来自该场地监测井(MW)的地下水样本进行了 GC-MS、终点 PCR 和定量 PCR(qPCR)分析,以检测生物标志物。代谢生物标志物包括特定的萘和/或 2-甲基萘厌氧降解中间产物:2-萘酸(2-NA);5,6,7,8-四氢-2-萘酸(TH-2-NA);六氢-2-萘酸(HH-2-NA);和羧化-2-甲基萘(MNA)。编码苯丁酰辅酶 A 合酶α亚基的基因 bssA 的类似物被用作遗传生物标志物。结果表明,受影响井中的总细菌丰度比未受影响井高 1-2 个数量级。使用简并引物的 bssA 基因终点 PCR 分析表明,在羽流范围内存在烃类降解细菌。在 qPCR 分析中,使用基于甲苯降解反硝化或硫酸盐还原/产甲烷细菌的引物,仅在 MW-24 中检测到 bssA 基因,MW-24 位于污染源下游。在多个井中检测到代谢生物标志物。MW-24 中也检测到 2-NA(6.7 μg/L)、TH-2-NA(2.6 μg/L)、HH-2-NA 和 MNA 的丰度最高。两种独立生物标志物的分布表明该场地富含厌氧烃生物降解,并为自然衰减提供了有力证据。

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