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恢复三氯乙烯污染土壤中的生化活性和细菌多样性:蚯蚓堆肥橄榄废弃物的修复效果

Restoring biochemical activity and bacterial diversity in a trichloroethylene-contaminated soil: the reclamation effect of vermicomposted olive wastes.

作者信息

Moreno Beatriz, Vivas Astrid, Nogales Rogelio, Macci Cristina, Masciandaro Grazia, Benitez Emilio

机构信息

Department of Environmental Protection, Estación Experimental del Zaidín (EEZ), CSIC, Profesor Albareda 1, 18008, Granada, Spain.

出版信息

Environ Sci Pollut Res Int. 2009 May;16(3):253-64. doi: 10.1007/s11356-008-0035-y. Epub 2008 Aug 27.

Abstract

BACKGROUND, AIM, AND SCOPE: In this work, the potential for using olive-mill solid waste as an organic amendment for biochemical and biological restoration of a trichloroethylene-contaminated soil, which has previously been stabilized through vermicomposting processes, has been explored.

MATERIALS AND METHODS

Trichloroethylene-contaminated water was pumped into soil columns with a layer of vermicompost at 10-cm depth (biobarrier system). The impacts of the trichloroethylene on the microbial community were evaluated by determining: (1) the overall microbial activity (estimated as dehydrogenase activity) and enzyme activities related to the main nutrient cycles (beta-glucosidase, o-diphenoloxidase, phosphatase, urease, and arylsulphatase activities). In addition, isoelectric focusing of the soil extracellular humic-beta-glucosidase complexes was performed to study the enzymatically active humic matter related to the soil carbon cycle. (2) The soil bacterial diversity and the molecular mechanisms for the bacterial resistance to organic solvents were also determined. For this, polymerase chain reaction (PCR)-denaturing gradient gel electrophoresis (DGGE) was used to detect changes in bacterial community structure and PCR-single-strand conformational polymorphism (SSCP) was developed and optimised for detection and discrimination of the resistance-nodulation-division (RND) genes amplified from the contaminated soils.

RESULTS

Vermicompost reduced, with respect to the unamended soil, about 30% of the trichloroethylene leaching during the first month of the experiment. Trichloroethylene had a marked negative effect on soil dehydrogenase, beta-glucosidase, urease, phosphatase, and arylsulphatase activities. Nevertheless, the vermicompost tended to avoid this toxic effect. Vermicompost also displays stable humic-beta-glucosidase complexes that increased the extracellular activity related to C-cycle in the contaminated soils. The isoelectric focusing technique showed a more biochemically active humic matter in the soil sampled under the vermicompost. The behaviour of the three main phyla of bacteria isolated from the DGGE bands was quite different. Bands corresponding to Actinobacteria disappeared, whereas those affiliated with Proteobacteria remained after the trichloroethylene contamination. The disappeared Actinobacteria became visible in the soil amended with the vermicompost. Bands corresponding to Bacteriodetes appeared only in columns of contaminated soils. In this study, six types of RND proteins were detected by PCR-SSCP in the natural soil, three in the trichloroethylene-contaminated soil and 7/5 in trichloroethylene-contaminated soil above/below the vermicompost in the biobarrier columns. Trichloroethylene tended to reduce or eliminate all the clones detected in the uncontaminated soil, whereas new efflux pumps appeared in the biobarrier columns.

DISCUSSION

Although enzymes incorporated into the humic substances of vermicomposted olive wastes are quite stable, trichloroethylene also inhibited the background levels of the soil extracellular beta-glucosidase activity in the amended soils. The decrease was less severe in the biobarrier system, but in any case, no relation was found between the levels of trichloroethylene in soil and extracellular beta-glucosidase activity, or between the latter and the quantity of humic carbon in soils. The isoelectric focusing technique was carried out in the humic fraction to determine whether the loss of activity occurred in overall extracellular beta-glucosidase or in that linked to stable humic substances (humic-enzyme complexes). The contaminated soils showed the lower enzyme activities, whereas contaminated and amended soils presented greater quantity of focalised (and therefore stable) humic carbon and spectra heterogeneity: very different bands with higher enzyme activities. No clear relationship between trichloroethylene concentration in soil and diversity of the bacterial population was noted. Similar patterns could be found when the community structures of bacteria and microbial activity were considered. Since the use of the dehydrogenase assay has been recognised as a useful indicator of the overall measure of the intensity of microbial metabolism, these results could be attributed to PCR-DGGE methodology, since the method reveals the presence of dominant populations regardless of their metabolic state. Trichloroethylene maintained or even increased the number of clones with the DNA encoding for RND proteins, except for the contaminated soil located above the vermicompost. However, the main effect of trichloroethylene was to modify the structure of the community in contaminated soils, considering the type of efflux pumps encoded by the DNA extracted from soil bacteria.

CONCLUSIONS

Trichloroethylene inhibited specific functions in soil and had a clear influence on the structure of the autochthonous bacterial community. The organic matter released by the vermicomposted olive waste tended to avoid the toxic effect of the contaminant. Trichloroethylene also inhibited the background levels of the soil extracellular beta-glucosidase activity, even when vermicompost was present. In this case, the effect of the vermicompost was to provide and/or to stimulate the humic-beta-glucosidase complexes located in the soil humic fraction >10(4), increasing the resistance of the enzyme to the inhibition. The bacterial community from the soil presented significantly different mechanisms to resistance to solvents (RND proteins) under trichloroethylene conditions. The effect of the vermicompost was to induce these mechanisms in the autochthonous bacterial community and/or incorporated new bacterial species, able to grow in a trichloroethylene-contaminated ambient. Coupled biochemical and molecular methodologies are therefore helpful approaches in assessing the effect of an organic amendment on the biochemical and biological restoration of a trichloroethylene-contaminated soil.

RECOMMENDATIONS AND PERSPECTIVES

Since the main biochemical and biological effects of the organic amendment on the contaminated soil seem to be the incorporation of biochemically active humic matter, as well as new bacterial species able to grow in a trichloroethylene-contaminated ambient, isoelectric focusing and PCR-SSCP methodologies should be considered as parts of an integrated approach to determine the success of a restoration scheme.

摘要

背景、目的和范围:在本研究中,探讨了利用橄榄果渣固体废弃物作为有机改良剂,对先前已通过蚯蚓堆肥过程稳定化的三氯乙烯污染土壤进行生化和生物修复的潜力。

材料与方法

将三氯乙烯污染的水泵入装有一层位于10厘米深度的蚯蚓堆肥的土壤柱中(生物屏障系统)。通过测定以下指标评估三氯乙烯对微生物群落的影响:(1)整体微生物活性(以脱氢酶活性估算)以及与主要养分循环相关的酶活性(β-葡萄糖苷酶、邻二酚氧化酶、磷酸酶、脲酶和芳基硫酸酯酶活性)。此外,对土壤细胞外腐殖质-β-葡萄糖苷酶复合物进行等电聚焦,以研究与土壤碳循环相关的具有酶活性的腐殖质。(2)还测定了土壤细菌多样性以及细菌对有机溶剂的抗性分子机制。为此,采用聚合酶链反应(PCR)-变性梯度凝胶电泳(DGGE)检测细菌群落结构的变化,并开发和优化了PCR-单链构象多态性(SSCP)方法,用于检测和鉴别从污染土壤中扩增出的抗性-结瘤-分裂(RND)基因。

结果

与未改良土壤相比,蚯蚓堆肥在实验的第一个月使三氯乙烯淋溶减少了约30%。三氯乙烯对土壤脱氢酶、β-葡萄糖苷酶、脲酶、磷酸酶和芳基硫酸酯酶活性有显著的负面影响。然而,蚯蚓堆肥倾向于避免这种毒性作用。蚯蚓堆肥还表现出稳定的腐殖质-β-葡萄糖苷酶复合物,增加了污染土壤中与碳循环相关的细胞外活性。等电聚焦技术显示,在蚯蚓堆肥下采样的土壤中腐殖质具有更高的生化活性。从DGGE条带中分离出的细菌三个主要门类的行为差异很大。对应放线菌的条带消失,而与变形菌门相关的条带在三氯乙烯污染后仍然存在。在添加蚯蚓堆肥的土壤中,消失的放线菌条带又可见了。对应拟杆菌门的条带仅出现在污染土壤柱中。在本研究中,通过PCR-SSCP在天然土壤中检测到六种类型的RND蛋白,在三氯乙烯污染土壤中检测到三种,在生物屏障柱中蚯蚓堆肥上方/下方的三氯乙烯污染土壤中分别检测到7/5种。三氯乙烯倾向于减少或消除在未污染土壤中检测到的所有克隆,而在生物屏障柱中出现了新的外排泵。

讨论

尽管掺入蚯蚓堆肥橄榄废弃物腐殖物质中的酶相当稳定,但三氯乙烯也抑制了改良土壤中土壤细胞外β-葡萄糖苷酶活性的背景水平。在生物屏障系统中这种降低不太严重,但无论如何,未发现土壤中三氯乙烯水平与细胞外β-葡萄糖苷酶活性之间,或后者与土壤中腐殖碳含量之间存在关联。对等电聚焦技术在腐殖质部分进行操作,以确定活性丧失是发生在整体细胞外β-葡萄糖苷酶中还是与稳定的腐殖物质(腐殖质-酶复合物)相关的酶中。污染土壤显示出较低的酶活性,而污染且改良的土壤呈现出更多聚焦(因此更稳定)的腐殖碳和光谱异质性:具有更高酶活性的非常不同的条带。未发现土壤中三氯乙烯浓度与细菌种群多样性之间存在明显关系。当考虑细菌群落结构和微生物活性时,可发现类似模式。由于脱氢酶测定法已被认为是微生物代谢强度总体测量的有用指标,这些结果可能归因于PCR-DGGE方法,因为该方法揭示了优势种群的存在,而不论其代谢状态如何。三氯乙烯维持甚至增加了编码RND蛋白的DNA克隆数量,但位于蚯蚓堆肥上方的污染土壤除外。然而,考虑从土壤细菌中提取的DNA编码的外排泵类型,三氯乙烯的主要作用是改变污染土壤中的群落结构。

结论

三氯乙烯抑制土壤中的特定功能,并对本地细菌群落结构有明显影响。蚯蚓堆肥橄榄废弃物释放的有机物质倾向于避免污染物的毒性作用。三氯乙烯也抑制了土壤细胞外β-葡萄糖苷酶活性的背景水平,即使存在蚯蚓堆肥也是如此。在这种情况下,蚯蚓堆肥的作用是提供和/或刺激位于土壤腐殖质部分>10(4)中的腐殖质-β-葡萄糖苷酶复合物,增加酶对抑制的抗性。在三氯乙烯条件下,土壤中的细菌群落对溶剂(RND蛋白)的抗性呈现出显著不同的机制。蚯蚓堆肥的作用是在本地细菌群落中诱导这些机制和/或引入能够在三氯乙烯污染环境中生长的新细菌物种。因此,结合生化和分子方法是评估有机改良剂对三氯乙烯污染土壤生化和生物修复效果的有用方法。

建议与展望

由于有机改良剂对污染土壤的主要生化和生物效应似乎是掺入具有生化活性的腐殖物质,以及引入能够在三氯乙烯污染环境中生长的新细菌物种,等电聚焦和PCR-SSCP方法应被视为确定修复方案成功与否的综合方法的一部分。

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