McClung C R, Chelm B K
J Bacteriol. 1987 Jul;169(7):3260-7. doi: 10.1128/jb.169.7.3260-3267.1987.
A genetic locus essential for the formate-dependent growth of Bradyrhizobium japonicum was isolated by complementation of ethyl methanesulfonate-induced mutants with a cosmid gene library of B. japonicum DNA. Three related cosmids containing 18.7 kilobase pairs of B. japonicum DNA in common were identified as being able to restore formate-dependent growth capability to mutants lacking either ribulosebisphosphate carboxylase or both ribulosebisphosphate carboxylase and phosphoribulokinase activities. To further localize the complementing gene(s), a series of four deletions spanning a total of 16.1 kilobase pairs were introduced into the B. japonicum chromosome. Each resulting deletion mutant lacked formate dehydrogenase activity and lacked ribulosebisphosphate carboxylase activity and immunologically detectable protein. Three of the four also lacked phosphoribulokinase activity. Two other mutants in which the deletion-bearing recombinant plasmid had integrated into the chromosome also lacked ribulosebisphosphate carboxylase activity and protein and phosphoribulokinase activities. The genetic locus defined by these mutants could contain the structural genes for these enzymes or a regulatory gene(s) controlling their expression or both.
通过用日本慢生根瘤菌DNA的黏粒基因文库对甲磺酸乙酯诱导的突变体进行互补,分离出了一个对日本慢生根瘤菌甲酸盐依赖型生长至关重要的基因座。鉴定出三个相关的黏粒,它们共含有18.7千碱基对的日本慢生根瘤菌DNA,能够将甲酸盐依赖型生长能力恢复到缺乏核酮糖二磷酸羧化酶或同时缺乏核酮糖二磷酸羧化酶和磷酸核酮糖激酶活性的突变体中。为了进一步定位互补基因,将一系列总共跨越16.1千碱基对的四个缺失片段导入日本慢生根瘤菌染色体。每个产生的缺失突变体都缺乏甲酸脱氢酶活性,缺乏核酮糖二磷酸羧化酶活性和免疫可检测的蛋白质。四个中的三个也缺乏磷酸核酮糖激酶活性。另外两个缺失携带重组质粒整合到染色体中的突变体也缺乏核酮糖二磷酸羧化酶活性、蛋白质和磷酸核酮糖激酶活性。这些突变体定义的基因座可能包含这些酶的结构基因或控制其表达的调控基因或两者都有。