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Application of Denaturing Gradient Gel Electrophoresis (DGGE) To Study the Diversity of Marine Picoeukaryotic Assemblages and Comparison of DGGE with Other Molecular Techniques

机译:变性梯度凝胶电泳(DGGE)在海洋微核真核生物多样性研究中的应用以及与其他分子技术的比较

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摘要

We used denaturing gradient gel electrophoresis (DGGE) to study the diversity of picoeukaryotes in natural marine assemblages. Two eukaryote-specific primer sets targeting different regions of the 18S rRNA gene were tested. Both primer sets gave a single band when used with algal cultures and complex fingerprints when used with natural assemblages. The reproducibility of the fingerprints was estimated by quantifying the intensities of the same bands obtained in independent PCR and DGGE analyses, and the standard error of these estimates was less than 2% on average. DGGE fingerprints were then used to compare the picoeukaryotic diversity in samples obtained at different depths and on different dates from a station in the southwest Mediterranean Sea. Both primer sets revealed significant differences along the vertical profile, whereas temporal differences at the same depths were less marked. The phylogenetic composition of picoeukaryotes from one surface sample was investigated by excising and sequencing DGGE bands. The results were compared with an analysis of a clone library and a terminal restriction fragment length polymorphism fingerprint obtained from the same sample. The three PCR-based methods, performed with three different primer sets, revealed very similar assemblage compositions; the same main phylogenetic groups were present at similar relative levels. Thus, the prasinophyte group appeared to be the most abundant group in the surface Mediterranean samples as determined by our molecular analyses. DGGE bands corresponding to prasinophytes were always found in surface samples but were not present in deep samples. Other groups detected were prymnesiophytes, novel stramenopiles (distantly related to hyphochytrids or labyrinthulids), cryptophytes, dinophytes, and pelagophytes. In conclusion, the DGGE method described here provided a reasonably detailed view of marine picoeukaryotic assemblages and allowed tentative phylogenetic identification of the dominant members.
机译:我们使用变性梯度凝胶电泳(DGGE)来研究天然海洋生物群中微核生物的多样性。测试了两个针对18S rRNA基因不同区域的真核生物特异性引物组。当与藻类培养物一起使用时,两个引物组都给出一个条带,而与自然组合物一起使用时,这两个引物组给出了复杂的指纹。指纹的可再现性是通过量化在独立PCR和DGGE分析中获得的相同谱带的强度来估计的,这些估计的标准误平均小于2%。然后,使用DGGE指纹图谱比较了从西南地中海某个站点在不同深度和不同日期获得的样本中的微核生物多样性。两种引物组均沿垂直剖面显示出显着差异,而在相同深度处的时间差异则不太明显。通过切除和测序DGGE条带,研究了来自一个表面样品的微核生物的系统发育组成。将结果与克隆文库的分析和从同一样品获得的末端限制性片段长度多态性指纹图谱进行比较。三种基于PCR的方法(使用三种不同的引物对)显示出非常相似的组合物组成。相同的主要系统发育组以相似的相对水平存在。因此,通过我们的分子分析确定,在地中海表面样品中,古植物植物群似乎是最丰富的。总是在表面样品中发现与藻类植物对应的DGGE条带,但在深层样品中却不存在。检出的其他组是扁桃体植物,新型层茎类(与疏水菌或唇草科密切相关),隐生植物,单生植物和pelagophytes。总而言之,此处描述的DGGE方法提供了海洋微核真核生物组合的合理详细视图,并允许对主要成员进行初步的系统发育鉴定。

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