rRNA based identification and detection systems for rhizobia and other bacteria

被引:40
作者
Ludwig, W [1 ]
Amann, R
Martinez-Romero, E
Schönhuber, W
Bauer, S
Neef, A
Schleifer, KH
机构
[1] Tech Univ Munich, Lehrstuhl Mikrobiol, D-80290 Munich, Germany
[2] Ctr Invest Sobre Fijac Nitrogeno, Cuernavaca, Morelos, Mexico
关键词
hybridization; in situ identification; phylogeny; probe design; rhizobia; rRNA;
D O I
10.1023/A:1004350708767
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Ribosomal ribonucleic acids are excellent marker molecules for the elucidation of bacterial phylogeny; they also provide useful target sites for identification and detection with nucleic acid probes. Based on the currently available 16S rRNA sequence data, bacteria of the rhizobial phenotype (plant nodulation, nitrogen fixation) are members of three moderately related phylogenetic sub-groups of the alpha-subclass of the Proteobacteria : i.e. the rhizobia group, the bradyrhizobia group, and the azorhizobia group. Ail rhizobia, azo-, brady-, meso- and sinorhizobia are closely related to and in some cases phylogenetically intermixed with, non-symbiotic and/or non-nitrogen-fixing bacteria. Especially in the case of Bradyrhizobium japonicum strains, the 16S rRNA sequence data indicate substantial heterogeneity. Specific probe design and evaluation are discussed. A multiprobe concept for resolving specificity problems with group specific probes is presented. In situ identification with group specific probes of rhizobia in cultures as well as rhizobia and cyanobacteria within plant material is shown.
引用
收藏
页码:1 / 19
页数:19
相关论文
共 80 条