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通过长距离核糖体分型对酿酒酵母进行菌种鉴定。

Saccharomyces species assignment by long range ribotyping.

作者信息

Messner R, Prillinger H

机构信息

Institute of Applied Microbiology, University of Agriculture, Wien, Austria.

出版信息

Antonie Van Leeuwenhoek. 1995;67(4):363-70. doi: 10.1007/BF00872936.

Abstract

Type strains of 10 genotypically distinct Saccharomyces species are differentiated by ribosomal DNA restriction fragment analysis (ribotyping). The full length of the chromosomal ribosomal repeat was amplified in two parts, the 18SrDNA including both ITS region (2600 bp) and the 25SrDNA (3300 bp). Restriction fragments generated by 9 enzymes from these two products yield characteristic patterns, by which unknown Saccharomyces isolates are assigned to the type strains. For convenient separation and detection only fragments longer than 200 bp were monitored. In contrast to molecular differentiation methods of highest resolution as RAPD-PCR or fingerprinting, the results from ribotyping are absolutely reproducible and thereby suitable for databases. The phylogeny computed from the discrete character matrix for presence/absence of fragments by the PHYLIP program package is in complete accordance to the phylogeny derived from ribosomal RNA sequence analysis. By this the field of application of the long range ribotyping can be regarded basically as equal to DNA sequence analysis of the same locus. Because distant relationships are recognized, misidentified genera were detected upon the species assignment. This cannot be done by methods of higher resolution like RAPD-PCR or fingerprinting.

摘要

通过核糖体DNA限制性片段分析(核糖体分型)可区分10种基因类型不同的酿酒酵母属物种的模式菌株。染色体核糖体重复序列的全长分两部分进行扩增,即包括ITS区域(2600 bp)的18S rDNA和25S rDNA(3300 bp)。这两种产物经9种酶产生的限制性片段呈现出特征性模式,据此可将未知的酿酒酵母分离株归为模式菌株。为便于分离和检测,仅监测长度超过200 bp的片段。与分辨率最高的分子分化方法如RAPD-PCR或指纹图谱不同,核糖体分型的结果具有绝对的可重复性,因此适用于数据库。通过PHYLIP程序包根据片段存在/缺失的离散特征矩阵计算出的系统发育与从核糖体RNA序列分析得出的系统发育完全一致。由此,长距离核糖体分型的应用领域基本上可被视为等同于同一基因座的DNA序列分析。由于能识别远缘关系,在物种归属时检测到了错误鉴定的属。这是分辨率更高的方法如RAPD-PCR或指纹图谱所无法做到的。

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