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Bioaugmentation of sequencing batch reactors for biological phosphorus removal: Comparative rRNA sequence analysis and hybridization with oligonucleotide probes

机译:测序分批反应器用于生物除磷的生物增强:比较性rRNA序列分析和与寡核苷酸探针的杂交

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Four laboratory-scale sequencing batch reactors (SBRs) were operated to evaluate whether bioaugmentation with Acinetobacter spp. can be used to improve start-up and performance of enhanced biological phosphorus removal (EBPR) systems. Two of the SBRs were bioaugmented during start-up by adding pure cultures of Acinetobacter spp., the third reactor received an amendment of activated sludge from a laboratory-scale EBPR system, and the fourth reactor, receiving no amendment, served as a control. Various chemical parameters were measured to monitor the performance of the four SBRS. Oligonucleotide probes of nested phylogenetic specificity were designed to quantify the contribution of Acinetobacter to EBPR. The probes were characterized for use in quantitative membrane hybridizations and fluorescent in situ hybridizations. Data from hybridizations with samples collected from the SBRs show declining levels of Acinetobacter spp. over the experiment. All four reactors achieved significant phosphorus removal and 90% nitrification after three days of operation. The results do not show a positive correlation between levels of Acinetobacter and successful EBPR. (C) 1998 IAWQ. Published by Elsevier Science Ltd. [References: 11]
机译:操作了四个实验室规模的分批测序反应器(SBR),以评估是否使用不动杆菌属进行生物增强。可用于改善增强型生物除磷(EBPR)系统的启动和性能。在启动过程中,通过添加不动杆菌属的纯培养物对其中的两个SBR进行了生物强化,第三个反应器从实验室规模的EBPR系统中获得了活性污泥的修正,而第四个反应器(没有修正)被作为对照。测量了各种化学参数以监测四个SBRS的性能。巢状系统发育特异性的寡核苷酸探针被设计来量化不动杆菌对EBPR的贡献。表征这些探针用于定量膜杂交和荧光原位杂交。与从SBR收集的样品杂交得到的数据显示不动杆菌属物种水平下降。在实验中。在运行三天后,所有四个反应器均实现了显着的除磷和90%的硝化。结果未显示不动杆菌水平与成功的EBPR之间呈正相关。 (C)1998 IAWQ。由Elsevier Science Ltd.发布[参考:11]

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