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DNA analyses of a private collection of microbial green algae contribute to a better understanding of microbial diversity

机译:私人收集的微生物绿藻的DNA分析有助于更好地了解微生物多样性

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Background DNA comparison is becoming the leading approach to the analysis of microbial diversity. For eukaryotes, the internal transcribed spacer 2 (ITS2) has emerged as a conspicuous molecule that is useful for distinguishing between species. Because of the small number of usable ITS data in GenBank, ITS2 sequence comparisons have only been used for limited taxa. However, major institutions with planktonic algal culture collections have now released small subunit (SSU) to ITS rDNA sequence data for their collections. This development has uplifted the level of molecular systematics for these algae. Results Forty-three strains of green algae isolated from German inland waters were investigated by using SSU-ITS rDNA sequencing. The strains were isolated through the direct plating method. Many of the strains went extinct during the years of culture. Thus, it could be expected that the surviving strains would be common, vigorous species. Nevertheless, 12 strains did not match any known species for which rDNA sequences had been determined. Furthermore, the identity of one strain was uncertain even at the genus level. Conclusions The aforementioned results show that long-forgotten and neglected collections may be of great significance in understanding microbial diversity, and that much work still needs to be done before the diversity of freshwater green algae can be fully described.
机译:背景DNA比较已成为分析微生物多样性的主要方法。对于真核生物,内部转录间隔区2(ITS2)已作为一种明显的分子出现,可用于区分物种。由于GenBank中可用的ITS数据较少,因此ITS2序列比较仅用于有限的分类单元。但是,具有浮游藻类培养物收集物的主要机构现在已将小亚基(SSU)发布到其收集物的ITS rDNA序列数据中。这种发展提高了这些藻类的分子系统学水平。结果采用SSU-ITS rDNA测序技术,对德国内陆水域分离出的43株绿藻进行了研究。通过直接铺板法分离菌株。在培养的岁月中,许多菌株灭绝了。因此,可以预期存活的菌株将是常见的有活力的物种。但是,有12个菌株与已确定rDNA序列的任何已知物种都不匹配。此外,即使在属水平,也不能确定一种菌株的身份。结论上述结果表明,长期被遗忘和被忽视的收集物对于理解微生物多样性可能具有重要意义,在充分描述淡水绿藻的多样性之前,仍需要做大量工作。

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