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邻苯二甲酸酯富集对污染土壤中多环芳烃生物降解的影响。

Effects of enrichment with phthalate on polycyclic aromatic hydrocarbon biodegradation in contaminated soil.

作者信息

Singleton David R, Richardson Stephen D, Aitken Michael D

机构信息

Department of Environmental Sciences and Engineering, School of Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Biodegradation. 2008 Jul;19(4):577-87. doi: 10.1007/s10532-007-9163-1. Epub 2007 Nov 8.

Abstract

The effect of enrichment with phthalate on the biodegradation of polycyclic aromatic hydrocarbons (PAH) was tested with bioreactor-treated and untreated contaminated soil from a former manufactured gas plant (MGP) site. Soil samples that had been treated in a bioreactor and enriched with phthalate mineralized (14)C-labeled phenanthrene and pyrene to a greater extent than unenriched samples over a 22.5-h incubation, but did not stimulate benzo[a]pyrene mineralization. In contrast to the positive effects on (14)C-labeled phenanthrene and pyrene, no significant differences were found in the extent of biodegradation of native PAH when untreated contaminated soil was incubated with and without phthalate amendment. Denaturing-gradient gel electrophoresis (DGGE) profiles of bacterial 16S rRNA genes from unenriched and phthalate-enriched soil samples were substantially different, and clonal sequences matched to prominent DGGE bands revealed that beta-Proteobacteria related to Ralstonia were most highly enriched by phthalate addition. Quantitative real-time PCR analyses confirmed that, of previously determined PAH-degraders in the bioreactor, only Ralstonia-type organisms increased in response to enrichment, accounting for 89% of the additional bacterial 16S rRNA genes resulting from phthalate enrichment. These findings indicate that phthalate amendment of this particular PAH-contaminated soil did not significantly enrich for organisms associated with high molecular weight PAH degradation or have any significant effect on overall degradation of native PAH in the soil.

摘要

采用来自某前制气厂(MGP)场地经生物反应器处理和未处理的污染土壤,测试了邻苯二甲酸盐富集对多环芳烃(PAH)生物降解的影响。在22.5小时的培养过程中,经生物反应器处理并富集了邻苯二甲酸盐的土壤样品比未富集的样品能更大量地矿化(14)C标记的菲和芘,但对苯并[a]芘的矿化没有促进作用。与对(14)C标记的菲和芘的积极影响相反,当未处理的污染土壤在添加和不添加邻苯二甲酸盐的情况下进行培养时,天然PAH的生物降解程度没有显著差异。未富集和邻苯二甲酸盐富集土壤样品的细菌16S rRNA基因的变性梯度凝胶电泳(DGGE)图谱有很大不同,与突出的DGGE条带匹配的克隆序列显示,与罗尔斯通氏菌相关的β-变形菌在添加邻苯二甲酸盐后富集程度最高。定量实时PCR分析证实,在生物反应器中先前确定的PAH降解菌中,只有罗尔斯通氏菌属的生物体因富集而增加,占邻苯二甲酸盐富集导致的额外细菌16S rRNA基因的89%。这些发现表明,对这种特定的PAH污染土壤添加邻苯二甲酸盐并没有显著富集与高分子量PAH降解相关的生物体,也对土壤中天然PAH的总体降解没有显著影响。

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