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引用次数: 16
摘要
我们在此展示厌氧氨氧化(厌氧氨氧化)细菌Candidatus (Ca.) Brocadia pituitae的第二个完整基因组,以及厌氧氨氧化细菌群落(ABC)元基因组中亚硝酸盐氧化剂和两个不完全反硝化菌的基因组。虽然NO2-还原为NO被认为是厌氧氨氧化的第一步,但Ca. B. pituitae缺乏负责这一反应的亚硝酸盐还原酶基因(nirK和nirS)。对垂体芽孢杆菌(Ca. B. pitu垂体)与库尼尼亚芽孢杆菌(Ca. Kuenenia stuttgartiensis)及其他6种接近完整基因组的厌氧氨氧化菌进行比较,发现它们的核心基因组结构包含1152个同源物。但核心缺失亚硝酸盐还原酶基因,而另外两种Brocadia具有nirK基因,并且这些基因是从多个谱系中水平获得的。相比之下,在核心中至少观察到5个相邻的羟胺氧化还原酶基因,其中含有编码另一种亚硝酸盐还原酶的候选基因(hao2和hao3)。事实上,这两个基因在Ca. B. pituitae和其他厌氧氨氧化菌中也显著表达。由于在ABC元基因组中检测到许多nirS和nirK基因,因此垂体Ca. B.可能不仅利用ABC成员提供的NO,还利用自身产生的NO和/或NH2OH进行厌氧氨氧化代谢。
The physiological potential of anammox bacteria as revealed by their core genome structure.
We present here the second complete genome of anaerobic ammonium oxidation (anammox) bacterium, Candidatus (Ca.) Brocadia pituitae, along with those of a nitrite oxidizer and two incomplete denitrifiers from the anammox bacterial community (ABC) metagenome. Although NO2- reduction to NO is considered to be the first step in anammox, Ca. B. pituitae lacks nitrite reductase genes (nirK and nirS) responsible for this reaction. Comparative genomics of Ca. B. pituitae with Ca. Kuenenia stuttgartiensis and six other anammox bacteria with nearly complete genomes revealed that their core genome structure contains 1,152 syntenic orthologues. But nitrite reductase genes were absent from the core, whereas two other Brocadia species possess nirK and these genes were horizontally acquired from multiple lineages. In contrast, at least five paralogous hydroxylamine oxidoreductase genes containing candidate ones (hao2 and hao3) encoding another nitrite reductase were observed in the core. Indeed, these two genes were also significantly expressed in Ca. B. pituitae as in other anammox bacteria. Because many nirS and nirK genes have been detected in the ABC metagenome, Ca. B. pituitae presumably utilises not only NO supplied by the ABC members but also NO and/or NH2OH by self-production for anammox metabolism.
期刊介绍:
DNA Research is an internationally peer-reviewed journal which aims at publishing papers of highest quality in broad aspects of DNA and genome-related research. Emphasis will be made on the following subjects: 1) Sequencing and characterization of genomes/important genomic regions, 2) Comprehensive analysis of the functions of genes, gene families and genomes, 3) Techniques and equipments useful for structural and functional analysis of genes, gene families and genomes, 4) Computer algorithms and/or their applications relevant to structural and functional analysis of genes and genomes. The journal also welcomes novel findings in other scientific disciplines related to genomes.