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利用土著降解菌成功地对受高氯酚污染的地下水进行好氧生物修复。

Successful aerobic bioremediation of groundwater contaminated with higher chlorinated phenols by indigenous degrader bacteria.

机构信息

Department of Environmental Sciences, University of Helsinki, Niemenkatu 73, 15140 Lahti, Finland; Department of Biological and Environmental Science, University of Jyväskylä, Survontie 9 C, 40500 Jyväskylä, Finland.

Department of Environmental Sciences, University of Helsinki, Niemenkatu 73, 15140 Lahti, Finland.

出版信息

Water Res. 2018 Jul 1;138:118-128. doi: 10.1016/j.watres.2018.03.033. Epub 2018 Mar 13.

Abstract

The xenobiotic priority pollutant pentachlorophenol has been used as a timber preservative in a polychlorophenol bulk synthesis product containing also tetrachlorophenol and trichlorophenol. Highly soluble chlorophenol salts have leaked into groundwater, causing severe contamination of large aquifers. Natural attenuation of higher-chlorinated phenols (HCPs: pentachlorophenol + tetrachlorophenol) at historically polluted sites has been inefficient, but a 4-year full scale in situ biostimulation of a chlorophenol-contaminated aquifer by circulation and re-infiltration of aerated groundwater was remarkably successful: pentachlorophenol decreased from 400 μg L to <1 μg L and tetrachlorophenols from 4000 μg L to <10 μg L. The pcpB gene, the gene encoding pentachlorophenol hydroxylase - the first and rate-limiting enzyme in the only fully characterised aerobic HCP degradation pathway - was present in up to 10% of the indigenous bacteria already 4 months after the start of aeration. The novel quantitative PCR assay detected the pcpB gene in situ also in the chlorophenol plume of another historically polluted aquifer with no remediation history. Hotspot groundwater HCPs from this site were degraded efficiently during a 3-week microcosm incubation with one-time aeration but no other additives: from 5400 μg L to 1200 μg L and to 200 μg L in lightly and fully aerated microcosms, respectively, coupled with up to 2400% enrichment of the pcpB gene. Accumulation of lower-chlorinated metabolites was observed in neither in situ remediation nor microcosms, supporting the assumption that HCP removal was due to the aerobic degradation pathway where the first step limits the mineralisation rate. Our results demonstrate that bacteria capable of aerobic mineralisation of xenobiotic pentachlorophenol and tetrachlorophenol can be present at long-term polluted groundwater sites, making bioremediation by simple aeration a viable and economically attractive alternative.

摘要

作为木材防腐剂,五氯苯酚曾被用于多氯苯酚的批量合成产品中,其中还包含四氯苯酚和三氯苯酚。高溶解性的氯苯酚盐已渗透到地下水中,致使大型含水层受到严重污染。在历史上受到污染的地点,高氯苯酚(HCP:五氯苯酚+四氯苯酚)的自然衰减效率低下,但通过循环和重新注入充氧地下水对受氯苯酚污染的含水层进行为期 4 年的原位生物刺激则非常成功:五氯苯酚的浓度从 400μg/L 降至<1μg/L,四氯苯酚的浓度从 4000μg/L 降至<10μg/L。pcpB 基因,即编码五氯苯酚羟化酶的基因——这是唯一完全表征的好氧 HCP 降解途径中的第一个和限速酶,在曝气开始后的 4 个月内,已存在于多达 10%的土著细菌中。新型定量 PCR 检测方法还在另一个历史上受到污染且没有修复历史的含水层的氯苯酚羽流中检测到了 pcpB 基因。该地点的热点地下水 HCPs 在为期 3 周的微宇宙培养中,通过一次性曝气但没有其他添加剂,得到了有效降解:在轻度和完全曝气的微宇宙中,分别从 5400μg/L 降至 1200μg/L 和 200μg/L,同时 pcpB 基因的丰度增加了 2400%。在原位修复或微宇宙中都没有观察到低氯代代谢物的积累,这支持了这样的假设,即 HCP 的去除是由于好氧降解途径,其中第一步限制了矿化速率。我们的研究结果表明,能够好氧矿化外来污染物五氯苯酚和四氯苯酚的细菌可能长期存在于受污染的地下水中,使得简单曝气的生物修复成为一种可行且具有经济吸引力的替代方案。

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