Dupuy N, Willems A, Pot B, Dewettinck D, Vandenbruaene I, Maestrojuan G, Dreyfus B, Kersters K, Collins M D, Gillis M
Laboratoire de Microbiologie des Sols, ORSTOM, Dakar, Senegal.
Int J Syst Bacteriol. 1994 Jul;44(3):461-73. doi: 10.1099/00207713-44-3-461.
Rhizobial isolates that were obtained from both surface and deep soil samples in the Sahelian and Sudano-Guinean areas of Senegal (West Africa) under Acacia albida trees were compared with representative strains of known rhizobial species and genera. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of proteins was used to determine the taxonomic positions of these organisms and the relationships between isolates obtained from the surface and isolates obtained from deep soil. Most of the isolates belonged to eight electrophoretic clusters containing representative strains of Bradyrhizobium japonicum, Bradyrhizobium elkanii, and Bradyrhizobium sp. Isolates were also characterized by the Biolog system, and the results were compared with the results obtained by SDS-PAGE of total proteins; the level of correlation was very low. DNA-rRNA hybridizations with 16S or 23S rRNA from Bradyrhizobium japonicum LMG 6138T (T = type strain) confirmed that most of the protein electrophoretic clusters belong in the Bradyrhizobium-Rhodopseudomonas rRNA complex. Sequencing of 16S rRNA genes showed that some of the A. albida-nodulating isolates belong to a separate lineage together with representatives of other protein electrophoretic clusters. Other isolates that belong to the same electrophoretic cluster as the type strain of Bradyrhizobium japonicum are considered members of the lineage represented by this type strain. The first lineage is as far removed from Bradyrhizobium japonicum as it is from the genus Afipia, Blastobacter denitrificans, and the genus Rhodopseudomonas. The possible relationship among electrophoretic group, geographic origin, and depth of isolation at a particular site is discussed.
从西非塞内加尔的萨赫勒地区和苏丹-几内亚地区的阿拉伯胶树(Acacia albida)下的表层和深层土壤样本中获取的根瘤菌分离物,与已知根瘤菌物种和属的代表性菌株进行了比较。利用蛋白质的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)来确定这些微生物的分类地位,以及从表层土壤和深层土壤中获得的分离物之间的关系。大多数分离物属于八个电泳簇,其中包含日本慢生根瘤菌(Bradyrhizobium japonicum)、埃氏慢生根瘤菌(Bradyrhizobium elkanii)和慢生根瘤菌属(Bradyrhizobium sp.)的代表性菌株。还通过Biolog系统对分离物进行了表征,并将结果与总蛋白SDS-PAGE获得的结果进行了比较;相关性水平非常低。与来自日本慢生根瘤菌LMG 6138T(T = 模式菌株)的16S或23S rRNA进行DNA-rRNA杂交,证实大多数蛋白质电泳簇属于慢生根瘤菌-红假单胞菌rRNA复合体。16S rRNA基因测序表明,一些能与阿拉伯胶树结瘤的分离物与其他蛋白质电泳簇的代表菌株属于一个单独的谱系。其他与日本慢生根瘤菌模式菌株属于同一电泳簇的分离物被认为是该模式菌株所代表的谱系的成员。第一个谱系与日本慢生根瘤菌的距离,与它与阿菲普亚菌属(Afipia)、反硝化芽孢杆菌(Blastobacter denitrificans)和红假单胞菌属(Rhodopseudomonas)的距离一样远。讨论了电泳组、地理来源和特定地点分离深度之间可能的关系。