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An investigation into the potential impacts of ocean acidification and ocean fertilisation on the genetic diversity of marine bacterial assemblages

机译:海洋酸化和海洋肥料对海洋细菌群落遗传多样性的潜在影响研究

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摘要

Based on the increase of 16S rRNA gene sequences in databases it is possible to design improved oligonucleotide primers for this gene. Primers were designed in silico to specifically amplify fragments of the gene from the Alpha, Beta and Gamma subgroups of the Proteobacteria, as well as from Bacteroidetes, Firmicutes, Cyanobacteria and Planctomycetes and tested in silico and in vitro. The aim was to investigate bacterioplankton diversity and reveal greater fingerprint diversity within these groups than is possible using primers specific for the entire domain Bacteria, and also to reduce clone library redundancy. It was then aimed to investigate the potential impacts of increased pCO2 and ocean fertilisation with iron (Fe) and phosphorus (P), on bacterioplankton diversity. Group-specific clone libraries representing contrasting marine regions were analysed, and the usefulness and specificity of the primers validated. The clone libraries showed members of the oligotrophic marine group (OMG) to be present in an in situ coastal mesocosm supplemented with nutrients. The newly-developed group-specific primers were used in combination with an improved method of denaturing gradient gel electrophoresis (DGGE) to profile in detail bacterial communities in mesocosms, which were maintained at 750 ppm of pCO2, the level projected for the global surface ocean in the year 3000, and 380 ppm of CO2, the present level. Increased pCO2 correlated with a decrease in abundance of some members of the Gammaproteobacteria. Otherwise there was little impact on diversity due to raised pCO2. The same DGGE protocol was applied to samples from an ocean Fe and P fertilisation experiment. Diversity change due to Fe was not evident. However in seawater amended with P there was an explosive growth of some cells with 16S rRNA genes similar to those of the SAR86 clade, and others with similarity to Gammaproteobacteria with large genomes such as Oceanospirillum sp. and Psychromonas sp.
机译:基于数据库中16S rRNA基因序列的增加,有可能为该基因设计改良的寡核苷酸引物。在计算机上设计引物,以特异性扩增来自变形杆菌的Alpha,Beta和Gamma子组以及拟杆菌,硬毛,蓝藻和浮游菌的基因片段,并在计算机和体外进行了测试。目的是研究浮游细菌的多样性,并揭示这些组内的指纹多样性,比使用对整个结构域细菌具有特异性的引物可能的指纹多样性更大,并且还减少了克隆文库的冗余性。然后旨在调查pCO2的增加以及铁(Fe)和磷(P)对海洋施肥对浮游生物多样性的潜在影响。分析了代表相反海洋区域的组特异性克隆文库,并验证了引物的有用性和特异性。克隆文库显示,贫营养海洋群(OMG)的成员存在于补充营养素的沿海近地膜中。新开发的组特异性引物与变性梯度凝胶电泳(DGGE)的改进方法结合使用,详细描绘了中膜中的细菌群落,其维持在750 ppm pCO2的水平,这是全球表层海洋预计的水平3000年和380 ppm的二氧化碳,目前的水平。 pCO2的增加与伽玛变形杆菌某些成员丰度的下降有关。否则,由于pCO2升高,对多样性几乎没有影响。将相同的DGGE协议应用于来自海洋铁和磷施肥实验的样品。铁引起的多样性变化不明显。但是,在用P修饰的海水中,一些具有16S rRNA基因的细胞呈爆炸性增长,类似于SAR86进化枝,并且其他与具有大型基因组的伽玛变形杆菌类似,例如Oceanospirillum sp。和Psychromonas sp。

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    Woolven-Allen John;

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  • 年度 2008
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  • 原文格式 PDF
  • 正文语种 English
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