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Identification of a novel subgroup of uncultured gammaproteobacterial glycogen-accumulating organisms in enhanced biological phosphorus removal sludge

机译:增强生物磷去除污泥中未衍生的甲状腺肿糖蓄血糖蓄能生物体的新亚组

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The presence of glycogen-accumulating organisms (GAO) has been hypothesized to be a cause of deterioration in enhanced biological phosphorus removal (EBPR) processes due to their abilities to out-compete polyphosphate-accumulating organisms (PAO). Based on 16S rRNA gene sequences, new members of uncultured gammaproteobacterial GAO (GB) were identified from sludge samples of a lab-scale sequencing batch reactor used for EBPR. The new GB formed a phylogenetic lineage (GB8) clearly distinct from the previously reported seven GB subgroups. Because the new GB8 members were not targeted by the known fluorescence in situ hybridization (FISH) oligonucleotide probes, a GB8-specific FISH probe (GB429) and a new FISH probe (GB742) targeting all eight GB subgroups were designed, and the phenotypic properties of the new GB8 members were investigated. FISH and microautoradiography approaches showed that GB429-targeted cells (GB8) were large coccobacilli (2–4 μm in size) with the ability to take up acetate under anaerobic conditions, but unable to accumulate polyphosphate under the subsequent aerobic conditions, consistent with in situ phenotypes of GB. FISH analyses on several sludge samples showed that members of GB8 were commonly detected as the majority of GB in lab- and full-scale EBPR processes. In conclusion, this study showed that members of GB8 could be a subgroup of GB with an important role in EBPR deterioration. Designs of FISH probes which hybridize with broader GB subgroups at different hierarchical levels will contribute to studies of the distributions and ecophysiologies of GB in lab- or full-scale EBPR plants.
机译:已经假设糖原累积生物(GAO)的存在是由于其在竞争的多磷酸盐积聚生物(PAO)的能力产生的增强的生物磷去除(EBPR)过程中的劣化原因。基于16S rRNA基因序列,从用于EBPR的实验室级测序批量反应器的污泥样品鉴定了未培养的γRoteobacterialGaO(GB)的新成员。新的GB形成了系统发育谱系(GB8)明显不同于先前报道的七个GB亚组。因为新的GB8成员未被已知的荧光原位杂交(鱼)寡核苷酸探针,所以设计了GB8特异性鱼探针(GB429)和靶向所有八个GB亚组的新鱼探针(GB742),以及表型特性调查了新的GB8成员。鱼类和微发造影方法表明,GB429靶向细胞(GB8)是大量的Cocobacilli(大小为2-4μm),其能够在厌氧条件下占醋酸盐,但不能在随后的有氧条件下积聚多磷酸盐,与原位一致GB的表型。几种污泥样品上的鱼分析显示,GB8的成员通常被检测为Lab和全规模EBPR过程中的大多数GB。总之,这项研究表明,GB8的成员可以是GB的亚组,具有EBPR恶化的重要作用。在不同层次水平下与更广泛的GB亚组杂交的鱼探测器将有助于研究GB在实验室或全规模EBPR植物中的GB分布和生态学。

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