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Diversity of Nitrite Reductase Genes in Candidatus Accumulibacter phosphatis-Dominated Cultures Enriched by Flow-Cytometric Sorting

机译:流式细胞分选法富集以磷脂酸杆菌为主体的亚硝酸盐还原酶基因的多样性

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摘要

“Candidatus Accumulibacter phosphatis” is considered a polyphosphate-accumulating organism (PAO) though it has not been isolated yet. To reveal the denitrification ability of this organism, we first concentrated this organism by flow cytometric sorting following fluorescence in situ hybridization (FISH) using specific probes for this organism. The purity of the target cells was about 97% of total cell count in the sorted sample. The PCR amplification of the nitrite reductase genes (nirK and nirS) from unsorted and sorted cells was performed. Although nirK and nirS were amplified from unsorted cells, only nirS was detected from sorted cells, indicating that “Ca. Accumulibacter phosphatis” has nirS. Furthermore, nirS fragments were cloned from unsorted (Ba clone library) and sorted (Bd clone library) cells and classified by restriction fragment length polymorphism analysis. The most dominant clone in clone library Ba, which represented 62% of the total number of clones, was not found in clone library Bd. In contrast, the most dominant clone in clone library Bd, which represented 59% of the total number of clones, represented only 2% of the total number of clones in clone library Ba, indicating that this clone could be that of “Ca. Accumulibacter phosphatis.” The sequence of this nirS clone exhibited less than 90% similarity to the sequences of known denitrifying bacteria in the database. The recovery of the nirS genes makes it likely that “Ca. Accumulibacter phosphatis” behaves as a denitrifying PAO capable of utilizing nitrite instead of oxygen as an electron acceptor for phosphorus uptake.
机译:尽管尚未分离出“ Candidatus Accumulibacter phosphatis”,但它仍被认为是一种聚磷酸盐蓄积生物(PAO)。为了揭示该生物的反硝化能力,我们首先通过流式细胞仪分选了该生物,然后使用该生物的特异性探针进行了荧光原位杂交(FISH)。目标细胞的纯度约为分选样品中细胞总数的97%。从未分选和分选的细胞中进行亚硝酸还原酶基因(nirK和nirS)的PCR扩增。尽管从未分选的细胞中扩增了nirK和nirS,但从分选的细胞中仅检测到nirS,表明“Ca。磷脂质杆菌”为nirS。此外,从未分选的(Ba克隆文库)克隆nirS片段,并从分选的(Bd克隆文库)细胞克隆nirS片段,并通过限制性片段长度多态性分析进行分类。在克隆文库Bd中未找到克隆文库Ba中占主导地位的克隆,占克隆总数的62%。相反,克隆文库Bd中占主导地位的克隆占克隆总数的59%,仅代表克隆文库Ba中克隆总数的2%,表明该克隆可能是“ Ca.磷脂质积累。”该nirS克隆的序列与数据库中已知反硝化细菌的序列显示出不到90%的相似性。 nirS基因的恢复可能使“Ca。磷脂质磷”起着反硝化PAO的作用,能够利用亚硝酸盐代替氧气作为磷的电子受体。

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