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Characterization and quantification of ammonia-oxidizing archaea (AOA) and bacteria (AOB) in a nitrogen-removing reactor using T-RFLP and qPCR

机译:使用T-RFLP和qPCR对脱氮反应器中氨氧化古细菌(AOA)和细菌(AOB)进行表征和定量

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摘要

Using ammonia monooxygenase α-subunit (amoA) gene and 16S rRNA gene, the community structure and abundance of ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB) in a nitrogen-removing reactor, which was operated for five phases, were characterized and quantified by cloning, terminal restriction fragment length polymorphism (T-RFLP), and quantitative polymerase chain reaction (qPCR). The results suggested that the dominant AOB in the reactor fell to the genus Nitrosomonas, while the dominant AOA belonged to Crenarchaeotal Group I.1a in phylum Crenarchaeota. Real-time PCR results demonstrated that the levels of AOB amoA varied from 2.9 × 103 to 2.3 × 105 copies per nanogram DNA, greatly (about 60 times) higher than those of AOA, which ranged from 1.7 × 102 to 3.8 × 103 copies per nanogram DNA. This indicated the possible leading role of AOB in the nitrification process in this study. T-RFLP results showed that the AOB community structure significantly shifted in different phases while AOA only showed one major peak for all the phases. The analyses also suggested that the AOB community was more sensitive than that of AOA to operational conditions, such as ammonia loading and dissolved oxygen.
机译:使用氨单加氧酶α亚基(amoA)基因和16S rRNA基因,将氨氧化古细菌(AOA)和氨氧化细菌(AOB)的群落结构和丰度进行了五个阶段的操作,通过克隆,末端限制性片段长度多态性(T-RFLP)和定量聚合酶链反应(qPCR)进行表征和定量。结果表明,反应器中的优势AOB属于亚硝化单胞菌属,而优势AOA属于Crenarchaeota门的Crnarchaeotal I.1a族。实时PCR结果表明,每纳克DNA的AOB amoA含量从2.9×10 3 到2.3×10 5 拷贝,大大高于(约60倍) AOA的拷贝数范围为每纳克DNA 1.7×10 2 至3.8×10 3 个拷贝。这表明在这项研究中AOB在硝化过程中可能发挥主导作用。 T-RFLP结果表明,AOB群落结构在不同阶段显着移动,而AOA在所有阶段仅显示一个主要峰。分析还表明,AOB社区比AOA对操作条件(例如氨负荷和溶解氧)更敏感。

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