Soybean and Alfalfa Research Laboratory, Agricultural Research Service, U.S. Department of Agriculture, Bldg. 011, HH-19, BARC-W, Beltsville, Maryland 20705-2350.
Appl Environ Microbiol. 1991 Dec;57(12):3496-501. doi: 10.1128/aem.57.12.3496-3501.1991.
Tn5 mutagenesis was coupled with a competition assay to isolate mutants of Bradyrhizobium japonicum defective in competitive nodulation. A double selection procedure was used, screening first for altered extracellular polysaccharide production (nonmucoid colony morphology) and then for decreased competitive ability. One mutant, which was examined in detail, was deficient in acidic polysaccharide and lipopolysaccharide production. The wild-type DNA region corresponding to the Tn5 insertion was isolated, mapped, and cloned. A 3.6-kb region, not identified previously as functioning in symbiosis, contained the gene(s) necessary for complementation of the mutation. The mutant was motile, grew normally on minimal medium, and formed nodules on soybean plants which fixed almost as much nitrogen as the wild type during symbiosis.
Tn5 突变与竞争测定相结合,以分离竞争结瘤缺陷的日本慢生根瘤菌突变体。采用双重选择程序,首先筛选改变的胞外多糖产生(非粘液菌落形态),然后筛选竞争能力降低。一个突变体被详细检查,它缺乏酸性多糖和脂多糖的产生。与 Tn5 插入相对应的野生型 DNA 区域被分离、作图和克隆。一个以前未被鉴定为在共生中起作用的 3.6kb 区域包含了互补突变所必需的基因。突变体是能动的,在最低培养基上正常生长,并在大豆植株上形成根瘤,在共生过程中固定的氮几乎与野生型相同。