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首页> 外文期刊>Applied and Environmental Microbiology >Genotypic Characterization ofBradyrhizobium Strains Nodulating Endemic Woody Legumes of the Canary Islands by PCR-Restriction Fragment Length Polymorphism Analysis of Genes Encoding 16S rRNA (16S rDNA) and 16S-23S rDNA Intergenic Spacers, Repetitive Extragenic Palindromic PCR Genomic Fingerprinting, and Partial 16S rDNA Sequencing
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Genotypic Characterization ofBradyrhizobium Strains Nodulating Endemic Woody Legumes of the Canary Islands by PCR-Restriction Fragment Length Polymorphism Analysis of Genes Encoding 16S rRNA (16S rDNA) and 16S-23S rDNA Intergenic Spacers, Repetitive Extragenic Palindromic PCR Genomic Fingerprinting, and Partial 16S rDNA Sequencing

机译:通过编码16S rRNA(16S rDNA)和16S-23S rDNA基因间隔子,重复的外基因回文PCR基因组指纹图谱和部分16S rDNA Sequence编码基因的PCR限制片段长度多态性分析,对加那利群岛特有木本豆科植物根瘤菌菌株进行基因型鉴定

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We present a phylogenetic analysis of nine strains of symbiotic nitrogen-fixing bacteria isolated from nodules of tagasaste (Chamaecytisus proliferus) and other endemic woody legumes of the Canary Islands, Spain. These and several reference strains were characterized genotypically at different levels of taxonomic resolution by computer-assisted analysis of 16S ribosomal DNA (rDNA) PCR-restriction fragment length polymorphisms (PCR-RFLPs), 16S-23S rDNA intergenic spacer (IGS) RFLPs, and repetitive extragenic palindromic PCR (rep-PCR) genomic fingerprints with BOX, ERIC, and REP primers. Cluster analysis of 16S rDNA restriction patterns with four tetrameric endonucleases grouped the Canarian isolates with the two reference strains, Bradyrhizobium japonicum USDA 110spc4 and Bradyrhizobium sp. strain (Centrosema) CIAT 3101, resolving three genotypes within these bradyrhizobia. In the analysis of IGS RFLPs with three enzymes, six groups were found, whereas rep-PCR fingerprinting revealed an even greater genotypic diversity, with only two of the Canarian strains having similar fingerprints. Furthermore, we show that IGS RFLPs and even very dissimilar rep-PCR fingerprints can be clustered into phylogenetically sound groupings by combining them with 16S rDNA RFLPs in computer-assisted cluster analysis of electrophoretic patterns. The DNA sequence analysis of a highly variable 264-bp segment of the 16S rRNA genes of these strains was found to be consistent with the fingerprint-based classification. Three different DNA sequences were obtained, one of which was not previously described, and all belonged to the B. japonicum/Rhodopseudomonas rDNA cluster. Nodulation assays revealed that none of the Canarian isolates nodulatedGlycine max or Leucaena leucocephala, but all nodulated Acacia pendula, C. proliferus,Macroptilium atropurpureum, and Vigna unguiculata.
机译:我们提出了九种菌株的共生固氮细菌的系统发育分析,这些细菌从塔加斯泰尔(Chamaecytisus proliferus)结节和西班牙加那利群岛的其他特有木本豆科植物中分离。通过计算机辅助分析16S核糖体DNA(rDNA)PCR-限制性片段长度多态性(PCR-RFLP),16S-23S rDNA基因间隔子(IGS)RFLP和不同基因组分辨率,对这些菌株和几种参考菌株进行了基因型鉴定。带有BOX,ERIC和REP引物的重复性外基因回文PCR(rep-PCR)基因组指纹。用四种四聚体核酸内切酶对16S rDNA限制性酶切图谱进行聚类分析,将Canarian分离株与两个参照菌株,日本慢生根瘤菌USDA 110spc4和慢生根瘤菌sp。分组。株(Centrosema)CIAT 3101,解决了这些缓生根瘤菌中的三种基因型。在用三种酶对IGS RFLP进行分析时,发现了六组,而rep-PCR指纹图谱显示出更大的基因型多样性,只有两个Canarian菌株具有相似的指纹图谱。此外,我们显示,通过在计算机辅助的电泳模式聚类分析中将它们与16S rDNA RFLP结合,可以将IGS RFLP甚至非常不同的rep-PCR指纹聚类为系统发育上合理的分组。发现这些菌株的16S rRNA基因的高度可变的264-bp片段的DNA序列分析与基于指纹的分类一致。获得了三个不同的DNA序列,其中一个以前没有描述过,并且全部属于日本芽孢杆菌/红景天rDNA簇。结瘤试验表明,没有一个加那利分离株结节为最大大豆或白头翁,而是所有结节的金合欢,C。proliferus,Macroptilium atropurpureum和Vigna unguiculata。

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