Russell P, Schell M G, Nelson K K, Halverson L J, Sirotkin K M, Stacey G
J Bacteriol. 1985 Dec;164(3):1301-8. doi: 10.1128/jb.164.3.1301-1308.1985.
The DNA region encoding early nodulation functions of Bradyrhizobium japonicum 3I1b110 (I110) was isolated by its homology to the functionally similar region from Rhizobium meliloti. Isolation of a number of overlapping recombinant clones from this region allowed the construction of a restriction map of the region. The identified nodulation region of B. japonicum shows homology exclusively to those regions of R. meliloti and Rhizobium leguminosarum DNA known to encode early nodulation functions. The region of homology with these two fast-growing Rhizobium species was narrowed to an 11.7-kilobase segment. A nodulation-defective mutant of Rhizobium fredii USDA 201, strain A05B-2, was isolated and found to be defective in the ability to curl soybean root hairs. Some of the isolated recombinant DNA clones of B. japonicum were found to restore wild-type nodulation function to this mutant. Analysis of the complementation results allows the identification of a 1.8-kilobase region as essential for restoration of Hac function.
通过与苜蓿中华根瘤菌功能相似区域的同源性,分离出了编码慢生根瘤菌3I1b110(I110)早期结瘤功能的DNA区域。从该区域分离出多个重叠的重组克隆,从而构建了该区域的限制性图谱。已鉴定出的慢生根瘤菌结瘤区域仅与苜蓿中华根瘤菌和豌豆根瘤菌中已知编码早期结瘤功能的那些区域具有同源性。与这两种快速生长的根瘤菌物种的同源区域被缩小到一个11.7千碱基的片段。分离出了费氏中华根瘤菌USDA 201的一个结瘤缺陷突变体A05B - 2,并发现其在卷曲大豆根毛的能力方面存在缺陷。一些分离出的慢生根瘤菌重组DNA克隆被发现能将该突变体的野生型结瘤功能恢复。对互补结果的分析使得能够鉴定出一个1.8千碱基的区域对于恢复结瘤功能是必不可少的。