Ramakrishnan N, Prakash R K, Shantharam S, Duteau N M, Atherly A G
J Bacteriol. 1986 Dec;168(3):1087-95. doi: 10.1128/jb.168.3.1087-1095.1986.
DNA hybridization with the cloned nodulation region of Rhizobium meliloti as a probe revealed DNA homology with four HindIII fragments, 12.5, 6.8, 5.2, and 0.3 kilobases (kb) in size, of the symbiotic plasmid pRjaUSDA193. Both hybridization and complementation studies suggest that the common nodulation genes nodABC and nodD of R. fredii USDA 193 are present on the 5.2-kb HindIII and 2.8-kb EcoRI fragments, respectively, of the Sym plasmid. Both fragments together could confer nodulation ability on soybeans when present in Sym plasmid-cured (Sym-) and wild-type (Sym+) Rhizobium strains or in a Ti plasmid-cured Agrobacterium tumefaciens strain. Furthermore, the 2.8-kb EcoRI fragment alone was able to form nodulelike structures on Glycine max L. cv. "Peking" (soybean). Microscopic examination of these nodules revealed bacterial invasion of the cells, probably via root hair penetration. Bacterial strains harboring plasmids carrying the 5.2- and 2.8-kb nod fragments elicited root-hair-curling responses on infection. These data suggest that the genes responsible for host range determination and some of the early events of nodulation may be coded for by the 5.2-kb HindIII and 2.8-kb EcoRI fragments.
以苜蓿根瘤菌克隆的结瘤区域为探针进行DNA杂交,结果显示与共生质粒pRjaUSDA193的4个HindIII片段(大小分别为12.5、6.8、5.2和0.3千碱基(kb))存在DNA同源性。杂交和互补研究均表明,费氏中华根瘤菌USDA 193的共同结瘤基因nodABC和nodD分别位于共生质粒的5.2-kb HindIII片段和2.8-kb EcoRI片段上。当这两个片段存在于共生质粒缺失(Sym-)和野生型(Sym+)根瘤菌菌株中,或存在于Ti质粒缺失的根癌土壤杆菌菌株中时,它们共同能够赋予大豆结瘤能力。此外,单独的2.8-kb EcoRI片段能够在大豆品种“北京”上形成类根瘤结构。对这些根瘤进行显微镜检查发现细菌侵入了细胞,可能是通过根毛穿透。携带含有5.2-kb和2.8-kb结瘤片段质粒的细菌菌株在感染时引发根毛卷曲反应。这些数据表明,负责宿主范围确定和结瘤早期一些事件的基因可能由5.2-kb HindIII和2.8-kb EcoRI片段编码。