首页> 外文期刊>Antonie van Leeuwenhoek: Journal of Microbiology and serology >Culture-independent nested PCR method reveals high diversity of actinobacteria associated with the marine sponges Hymeniacidon perleve and Sponge sp.
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Culture-independent nested PCR method reveals high diversity of actinobacteria associated with the marine sponges Hymeniacidon perleve and Sponge sp.

机译:不依赖于培养的嵌套式PCR方法揭示了与海洋海绵Hymeniacidon perleve和Sponge sp。相关的放线菌的多样性。

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A culture-independent nested polymerase chain reaction (PCR) technique was used to investigate the diversity of actinobacteria communities associated with the sponges Hymeniacidon perleve and Sponge sp. The phylogenetic affiliation of sponge-derived actinobacteria was then assessed by 16S rRNA sequencing of cloned DNA fragments. A total of 196 positive clones were screened by restriction fragment length polymorphism (RFLP) analysis; 48 unique operational taxonomic units (OTUs) were selected for sequencing. Rarefaction analysis indicated that the clone libraries represented 93% and 94% of the total estimated diversity for the two species, respectively. Phylogenetic analysis of sequence data revealed representatives of various phylogenetic divisions, which were related to the following ten actinobacterial genera: Acidimicrobium, Corynebacterium, Propionibacterium, Actinomyces, Micrococcus, Microbacterium, Streptomyces, Mycobacterium, Cellulosimicrobium, Sporichthya, and unidentified actinobacterial clones. A sponge-specific, previously uncultured actinobacteria community grouped within the subclass Acidimicrobidae was discovered from both H. perleve and Sponge sp. Sequences belonging to Acidimicrobium in the H. perleve and the Sponge sp. clone libraries represented 33% and 24% of the clones, respectively. In the Sponge sp. clone library Mycobacterium dominated, accounting for 70% of all clones. The presence of Acidimicrobium and mycobacteria within two sponges can lay the groundwork for attempts to culture these interesting bacteria for industrial applications.
机译:不依赖于培养的巢式聚合酶链反应(PCR)技术用于研究与海绵Hymeniacidon perleve和Sponge sp相关的放线菌群落的多样性。然后通过克隆的DNA片段的16S rRNA测序评估海绵来源的放线菌的系统亲缘关系。通过限制性片段长度多态性(RFLP)分析筛选了总共196个阳性克隆。选择了48个独特的操作分类单位(OTU)进行测序。 Rarefaction分析表明,克隆文库分别代表了两个物种总估计多样性的93%和94%。序列数据的系统发生分析揭示了与以下十个放线菌属有关的各种系统发生学划分的代表:酸性细菌,棒状杆菌,丙酸杆菌,放线菌,微球菌,微细菌,链霉菌,分枝杆菌,纤维素杆菌,Sporichthya和未鉴定的放线菌克隆。在H. perleve和Sponge sp。中都发现了一个海绵特定的,以前未培养的放线菌群落,该群落归类于酸性小杆菌科。属于H. perleve和Sponge sp。的Acidimicrobium的序列。克隆文库分别代表克隆的33%和24%。在海绵sp。克隆文库以分枝杆菌为主导,占所有克隆的70%。在两个海绵中存在酸性细菌和分枝杆菌可以为尝试将这些有趣的细菌用于工业应用奠定基础。

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