Vinuesa P, Rademaker J L, de Bruijn F J, Werner D
Fachbereich Biologie, Fachgebiet Angewandte Botanik und Zellbiologie, Philipps-Universität Marburg, D-35032 Marburg, Germany.
Appl Environ Microbiol. 1998 Jun;64(6):2096-104. doi: 10.1128/AEM.64.6.2096-2104.1998.
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 nodulated Glycine max or Leucaena leucocephala, but all nodulated Acacia pendula, C. proliferus, Macroptilium atropurpureum, and Vigna unguiculata.
我们对从西班牙加那利群岛的银荆(Chamaecytisus proliferus)及其他本地木本豆科植物根瘤中分离出的9株共生固氮细菌进行了系统发育分析。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基因间隔区(IGS)RFLP以及使用BOX、ERIC和REP引物的重复外显子回文PCR(rep-PCR)基因组指纹图谱,在不同分类分辨率水平上对这些菌株以及几个参考菌株进行了基因型鉴定。用四种四聚体核酸内切酶对16S rDNA限制性图谱进行聚类分析,将加那利群岛分离株与两个参考菌株——慢生根瘤菌大豆USDA 110spc4和慢生根瘤菌属(Centrosema)菌株CIAT 3101归为一类,在这些慢生根瘤菌中分辨出三种基因型。在用三种酶进行IGS RFLP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,加那利群岛菌株中只有两株具有相似的指纹图谱。此外,我们还表明,通过在计算机辅助的电泳图谱聚类分析中将IGS RFLP以及甚至非常不同的rep-PCR指纹图谱与16S rDNA RFLP相结合,可以将它们聚类为系统发育合理的分组。对这些菌株16S rRNA基因高度可变的264 bp片段进行DNA序列分析,结果与基于指纹图谱的分类一致。获得了三种不同的DNA序列,其中一种以前未描述过,所有序列均属于大豆慢生根瘤菌/红假单胞菌rDNA聚类。结瘤试验表明,加那利群岛分离株均不能使大豆或银合欢结瘤,但都能使垂枝相思、银荆、紫花大翼豆和豇豆结瘤。