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Changes in salt marsh sediment microbial community structure in response to petroleum contamination.

机译:盐沼沉积物微生物群落结构对石油污染的响应变化。

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Traditional and molecular techniques using a variety of indices including bacterial plate counts, MPNs, and DNA-DNA hybridizations were implemented to assess changes in microbial communities in oil-contaminated marine sediments and in sediments undergoing bioremediation with several commercial products. All studies were conducted using sediment microcosms. Microbial DNA was extracted from the sediment using a modified version of direct DNA extraction. With this procedure the efficiency of cell lysis was greater than 95% and the average amount of DNA extracted was 5 to 8 μg/g sediment. However, the extracted DNA was colored (dark red) and required purification by electroelution prior to subsequent molecular analysis. Humic material (>2.0 μg) inhibited the binding of target DNA onto nylon membranes and decreased the efficiency of target DNA detection during hybridizations. Testing of oil-bioremedation products indicated that inorganic nutrient amendment was the most effective treatment for enhancement of oil degradation. Enhanced oil-degradation was associated with increases in the amount of extractable microbial DNA in the sediment, although not with increased viable counts (plate counts, MPN) of oil degraders, or of individual bacterial populations as detected by oligonucleotide probes. In another set of microcosm studies, the proportions of oil-degrading bacteria increased >100 fold in oil amended microcosms and >10 fold in plant detritus or oil + plant detritus amended microcosms compared to that of intact sediments. DNA-hybridizations of extractable DNA from sediments with Bacteria, Archaea and Eukarya oligonucleotide probes indicated little changes in the sediment community resulting from petroleum contamination. In contrast, bacterial community rDNA hybridization similarity indices, indicated that bacterial diversity in oil contaminated sediments decreased after one month. However, after three months the bacterial diversity of oil impacted-sediment increased toward that of the unamended control. Analysis of the bacterial communities by rDNA-hybridization was in agreement with analyses of sediment oil-degrading bacteria by MPN and petroleum degradation by GC/MS. Suggesting that as levels of petroleum contamination decreased in the sediment, the bacterial community structure returned toward the bacterial community of uncontaminated marine sediment.
机译:实施了传统和分子技术,使用了包括细菌平板计数,MPN和DNA-DNA杂交在内的多种指标,以评估受油污染的海洋沉积物中以及经过几种商业产品进行生物修复的沉积物中微生物群落的变化。所有研究都是使用沉积物微观世界进行的。使用直接DNA提取的改进版本从沉积物中提取微生物DNA。通过该程序,细胞裂解效率大于95%,平均提取的DNA量为5至8μg/ g沉淀物。但是,提取的DNA是彩色的(深红色),需要在随后的分子分析之前通过电洗脱纯化。腐殖质材料(> 2.0μg)抑制了目标DNA与尼龙膜的结合,并降低了杂交过程中目标DNA检测的效率。石油生物修复产品的测试表明,无机营养改良剂是增强油脂降解的最有效方法。油的降解增强与沉积物中可提取的微生物DNA量的增加有关,尽管与油降解剂或寡核苷酸探针检测到的单个细菌种群的活数(板数,MPN)增加无关。在另一组微观世界研究中,与完整的沉积物相比,在经过油修正的微观世界中,降解油脂的细菌的比例增加了> 100倍,而在植物碎屑或油+植物碎屑的微观世界中,降解了石油的细菌的比例增加了10倍以上。用细菌,古细菌和Eukarya寡核苷酸探针对沉积物中的可提取DNA进行DNA杂交表明,石油污染导致沉积物群落几乎没有变化。相反,细菌群落rDNA杂交相似性指数表明,受油污染的沉积物中细菌的多样性在一个月后下降。但是,三个月后,受油污沉积物的细菌多样性向未经修正的对照组增加。通过rDNA杂交分析细菌群落与通过MPN分析沉积物降解石油的细菌以及通过GC / MS分析石油降解的观点一致。这表明随着沉积物中石油污染水平的降低,细菌群落结构返回到未污染的海洋沉积物的细菌群落。

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