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豆科根瘤菌相对于其他根瘤菌和土壤杆菌的系统发育。

Phylogeny of Rhizobium galegae with respect to other rhizobia and agrobacteria.

作者信息

Terefework Z, Nick G, Suomalainen S, Paulin L, Lindström K

机构信息

Department of Applied Chemistry and Microbiology, University of Helsinki, Finland.

出版信息

Int J Syst Bacteriol. 1998 Apr;48 Pt 2:349-56. doi: 10.1099/00207713-48-2-349.

Abstract

PCR-RFLP with nine restriction enzymes was applied to the 16S and 23S rRNA genes of 42 rhizobial and agrobacterial strains to determine the phylogenetic position of Rhizobium galegae and increase the understanding of the evolution of ribosomal operons. The strains were selected based on previous phylogenetic studies. PCR primers were designed so that they amplified a 2.3 kb fragment of the 23S rRNA gene (excluding the B8 loop). Universal primers rD1 and fD1 were used to amplify the full-length 16S rRNA. The RFLP analysis resulted in 27 and 32 different restriction patterns for 16S and 23S, respectively. The RFLP patterns were transformed to genetic distances and dendrograms were constructed from the data using the unweighted pair group method with averages. The shapes of the dendrograms derived from the analysis of the 16S and 23S rRNA genes correlated well, with only a few strains having different positions. The 23S tree generally had deeper branching than the 16S tree, allowing better discrimination between species and strains. The combined data from the two analyses described 36 genotypes. The eight R. galegae strains formed a homogeneous cluster in all dendrograms. The RFLP analysis was confirmed by partial sequence analysis of the 16S rRNA gene (the first 800 bp), which correlated well with full-length 16S rRNA sequence analysis. The 16S data placed R. galegae near the genus Agrobacterium with Agrobacterium vitis as its nearest neighbour, whereas in the 23S and the combined dendrograms it showed closer affinity to the genus Rhizobium.

摘要

运用9种限制性内切酶的PCR-RFLP技术,对42株根瘤菌和土壤杆菌菌株的16S和23S rRNA基因进行分析,以确定加杨根瘤菌的系统发育位置,并增进对核糖体操纵子进化的理解。这些菌株是根据先前的系统发育研究挑选出来的。设计了PCR引物,使其扩增出23S rRNA基因的一个2.3 kb片段(不包括B8环)。通用引物rD1和fD1用于扩增全长16S rRNA。RFLP分析分别产生了16S和23S的27种和32种不同的限制性图谱。将RFLP图谱转换为遗传距离,并使用非加权平均法根据数据构建系统发育树状图。由16S和23S rRNA基因分析得出的树状图形状相关性良好,只有少数菌株位置不同。23S树状图的分支通常比16S树状图更深,能更好地区分物种和菌株。两种分析的合并数据描述了36种基因型。8株加杨根瘤菌菌株在所有树状图中形成了一个同质簇。通过对16S rRNA基因(前800 bp)的部分序列分析证实了RFLP分析结果,该分析与全长16S rRNA序列分析相关性良好。16S数据显示加杨根瘤菌与土壤杆菌属接近,其中葡萄土壤杆菌是其最接近的邻居,而在23S和合并的树状图中,它与根瘤菌属显示出更密切的亲缘关系。

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