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Thermal Gradient Gel Electrophoresis Analysis of Bioprotection from Pollutant Shocks in the Activated Sludge Microbial Community

机译:活性污泥微生物群落中生物保护免受污染物冲击的热梯度凝胶电泳分析

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We used a culture-independent approach, namely, thermal gradient gel electrophoresis (TGGE) analysis of ribosomal sequences amplified directly from community DNA, to determine changes in the structure of the microbial community following phenol shocks in the highly complex activated sludge ecosystem. Parallel experimental model sewage plants were given shock loads of chlorinated and methylated phenols and simultaneously were inoculated (i) with a genetically engineered microorganism (GEM) able to degrade the added substituted phenols or (ii) with the nonengineered parental strain. The sludge community DNA was extracted, and 16S rDNA was amplified and analyzed by TGGE. To allow quantitative analysis of TGGE banding patterns, they were normalized to an external standard. The samples were then compared with each other for similarity by using the coefficient of Dice. The Shannon index of diversity, H, was calculated for each sludge sample, which made it possible to determine changes in community diversity. We observed a breakdown in community structure following shock loads of phenols by a decrease in the Shannon index of diversity from 1.13 to 0.22 in the noninoculated system. Inoculation with the GEM (Pseudomonas sp. strain B13 SN45RE) effectively protected the microbial community, as indicated by the maintenance of a high diversity throughout the shock load experiment (Hdecreased from 1.03 to only 0.82). Inoculation with the nonengineered parental strain, Pseudomonas sp. strain B13, did not protect the microbial community from being severely disturbed;H decreased from 1.22 to 0.46 for a 3-chlorophenol–4-methylphenol shock and from 1.03 to 0.70 for a 4-chlorophenol–4-methylphenol shock. The catabolic trait present in the GEM allowed for bioprotection of the activated sludge community from breakdown caused by toxic shock loading. In-depth TGGE analysis with similarity and diversity algorithms proved to be a very sensitive tool to monitor changes in the structure of the activated sludge microbial community, ranging from subtle shifts during adaptation to laboratory conditions to complete collapse following pollutant shocks.
机译:我们使用了一种与文化无关的方法,即对从群落DNA直接扩增的核糖体序列进行热梯度凝胶电泳(TGGE)分析,以确定在高度复杂的活性污泥生态系统中苯酚冲击后微生物群落结构的变化。对平行的实验模型污水处理厂施加氯和甲基化苯酚的冲击负荷,并同时(i)用能够降解添加的取代酚的基因工程微生物(GEM)或(ii)用非工程亲本菌株接种。提取污泥群落DNA,并用TGGE扩增和分析16S rDNA。为了对TGGE谱带图谱进行定量分析,将其标准化为外部标准。然后使用Dice系数将样本彼此进行相似性比较。计算每个污泥样品的香农多样性指数H,这使得确定群落多样性的变化成为可能。我们观察到,在非接种系统中,苯酚的冲击负荷后,香农多样性指数从1.13下降到0.22,从而破坏了群落结构。在整个冲击负荷实验中保持高多样性(H值从1.03降低到仅0.82)表明,GEM(假单胞菌属B13 SN45RE菌株)的接种有效地保护了微生物群落。接种非工程亲本品系假单胞菌(Pseudomonas sp。)菌株B13不能保护微生物群落免受严重干扰;对于3-氯苯酚-4-甲基苯酚冲击,H从1.22降低到0.46;对于4-氯苯酚-4-甲基苯酚冲击,H从1.03下降到0.70。 GEM中存在的分解代谢特性可对活性污泥群落进行生物保护,使其免受毒性冲击负荷引起的破坏。事实证明,采用相似性和多样性算法进行的深入TGGE分析是监测活化污泥微生物群落结构变化的非常灵敏的工具,其范围从适应实验室条件期间的细微变化到污染物冲击后完全崩塌。

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