Kranz R G, Haselkorn R
Gene. 1985;40(2-3):203-15. doi: 10.1016/0378-1119(85)90043-5.
Translational fusions of the Escherichia coli lacZYA operon to Rhodopseudomonas capsulata nif genes were obtained by using mini-MudII1734 [Castilho et al., J. Bacteriol. 158 (1984) 488-495] inserts into cloned fragments of R. capsulata DNA. A lac fusion to the nifH gene, which encodes dinitrogenase reductase, was used to classify Nif- mutations occurring in regulatory genes. Nine mutations were unable to activate nifHDK transcription. The nine mutations define four nif regulatory genes. Three of these genes are located on the same R. capsulata 8.4-kb EcoRI fragment. Each is transcribed independently. One of these (complementing mutant J61) is partially homologous with the ntrC gene of Escherichia coli, based on Southern hybridization. The fourth nif regulatory gene (complementing mutants LJ1, AH1 and AH3) is unlinked to the others. Lac fusions to all four regulatory genes were constructed. Each regulatory gene is weakly expressed compared to derepressed nifH and partially repressed in the presence of ammonia.
通过将mini - MudII1734[卡斯蒂略等人,《细菌学杂志》158(1984)488 - 495]插入荚膜红假单胞菌DNA的克隆片段中,获得了大肠杆菌lacZYA操纵子与荚膜红假单胞菌nif基因的翻译融合体。一个与编码固氮酶还原酶的nifH基因的lac融合体被用于对调控基因中发生的Nif - 突变进行分类。九个突变无法激活nifHDK转录。这九个突变定义了四个nif调控基因。其中三个基因位于同一荚膜红假单胞菌8.4kb的EcoRI片段上。每个基因都是独立转录的。基于Southern杂交,其中一个基因(互补突变体J61)与大肠杆菌的ntrC基因部分同源。第四个nif调控基因(互补突变体LJ1、AH1和AH3)与其他基因不连锁。构建了与所有四个调控基因的lac融合体。与去阻遏的nifH相比,每个调控基因的表达都较弱,并且在有氨存在的情况下会部分受到抑制。