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Takashi Nakase's last tweet: what is the current direction of microbial taxonomy research?

机译:Takashi Nakase的最后推文:当前的微生物分类学研究是什么?

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During the last few decades, type strains of most yeast species have been barcoded using the D1/D2 domain of their LSU rRNA gene and internal transcribed spacer (ITS) region. Species identification using DNA sequences regarding conspecificity in yeasts has also been studied. Most yeast species can be identified according to the sequence divergence of their ITS region or a combination of the D1/D2 and ITS regions. Studies that have examined intraspecific diversity have used multilocus sequence analyses, whereas the marker regions used in this analysis vary depending upon taxa. D1/D2 domain and ITS region sequences have been used as barcodes to develop primers suitable for the detection of the biological diversity of environmental DNA and the microbiome. Using these barcode sequences, it is possible to identify relative lineages and infer their gene products and function, and how they adapt to their environment. If barcode sequence was not variable enough to identify a described species, one could investigate the other biological traits of these yeasts, considering geological distance, environmental circumstances and isolation of reproduction. This article is dedicated to late Dr Takashi Nakase (1939-2018).
机译:在过去的几十年中,使用LSU RRNA基因的D1 / D2结构域和内转录的间隔区(其)区域的D1 / D2结构型,大多数酵母物种的类型菌株。还研究了使用关于酵母在酵母中的尖锐性的DNA序列的物种鉴定。大多数酵母物种可以根据其区域的序列分歧或D1 / D2及其区域的组合鉴定。检查内部分集的研究使用了多点序列分析,而该分析中使用的标记区域因分类而异。 D1 / D2结构域及其区域序列已被用作条形码,以开发适合于检测环境DNA和微生物组的生物多样性的引物。使用这些条形码序列,可以识别相对谱系和推断它们的基因产品和功能,以及它们如何适应其环境。如果条形码序列不足以鉴定所描述的物种,则可以研究这些酵母的其他生物学性状,考虑到地质距离,环境情况和繁殖的分离。本文专门致力于Takashi Nakase博士(1939-2018)。

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