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Identification of a Novel Group of Bacteria in Sludge from a Deteriorated Biological Phosphorus Removal Reactor

机译:从恶化的生物除磷反应器污泥中的新型细菌的鉴定。

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摘要

The microbial diversity of a deteriorated biological phosphorus removal reactor was investigated by methods not requiring direct cultivation. The reactor was fed with media containing acetate and high levels of phosphate (P/C weight ratio, 8:100) but failed to completely remove phosphate in the effluent and showed very limited biological phosphorus removal activity. Denaturing gradient gel electrophoresis (DGGE) of PCR-amplified 16S ribosomal DNA was used to investigate the bacterial diversity. Up to 11 DGGE bands representing at least 11 different sequence types were observed; DNA from the 6 most dominant of these bands was further isolated and sequenced. Comparative phylogenetic analysis of the partial 16S rRNA sequences suggested that one sequence type was affiliated with the alpha subclass of the Proteobacteria, one was associated with the Legionella group of the gamma subclass of the Proteobacteria, and the remaining four formed a novel group of the gamma subclass of the Proteobacteria with no close relationship to any previously described species. The novel group represented approximately 75% of the PCR-amplified DNA, based on the DGGE band intensities. Two oligonucleotide rRNA probes for this novel group were designed and used in a whole-cell hybridization analysis to investigate the abundance of this novel group in situ. The bacteria were coccoid and 3 to 4 μm in diameter and represented approximately 35% of the total population, suggesting a relatively close agreement with the results obtained by the PCR-based DGGE method. Further, based on electron microscopy and standard staining microscopic analysis, this novel group was able to accumulate granule inclusions, possibly consisting of polyhydroxyalkanoate, inside the cells.
机译:通过不需要直接培养的方法研究了退化的生物除磷反应器的微生物多样性。向反应器中加入了含有乙酸盐和高水平磷酸盐(P / C重量比,8:100)的介质,但未能完全去除废水中的磷酸盐,并且显示出非常有限的生物除磷活性。 PCR扩增的16S核糖体DNA的变性梯度凝胶电泳(DGGE)用于研究细菌多样性。观察到多达11个代表至少11种不同序列类型的DGGE谱带;来自这些条带中最重要的6条的DNA被进一步分离和测序。对部分16S rRNA序列进行的比较系统发育分析表明,一种序列类型与变形杆菌的alpha子类相关,一种序列与变形杆菌的gamma子类的军团菌相关,其余四种组成了一个新的gamma组。变形杆菌的一个亚类,与任何先前描述的物种没有密切关系。基于DGGE条带强度,该新组代表了约75%的PCR扩增DNA。设计了用于该新组的两种寡核苷酸rRNA探针,并将其用于全细胞杂交分析中,以原位研究该新组的丰度。细菌为类球菌,直径为3至4μm,约占总种群的35%,表明与基于PCR的DGGE方法获得的结果相对接近。此外,基于电子显微镜和标准染色显微镜分析,该新组能够在细胞内积聚可能由多羟基链烷酸酯组成的颗粒内含物。

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