Zinchenko V V, Kopteva A V, Frolova V D, Shestakov S V
Genetika. 1988 Jun;24(6):998-1007.
The genes glnA, ntr, nif or their promoters from Klebsiella pneumoniae cloned on the vectors, based on the plasmid RSF1010, were introduced into Rhodobacter sphaeroides cells. It was found that K. pneumoniae genes glnA, nifB, nifE, nifL and nifH are not expressed in R. sphaeroides. Neither was the glnA gene from cyanobacterium Anabaena 7120 expressed in R. sphaeroides. No functional activity of K. pneumoniae product of ntrA gene which is expressed from its own promoter, and the product of the gene nifA which is expressed from the constitutive promoter of the kanamycin resistance gene of the transposon Tn903, was detected. The implications of these findings are discussed.
将基于质粒RSF1010构建的载体上克隆的肺炎克雷伯菌的谷氨酰胺合成酶基因(glnA)、氮调节基因(ntr)、固氮基因(nif)或其启动子导入球形红杆菌细胞。结果发现,肺炎克雷伯菌的glnA、nifB、nifE、nifL和nifH基因在球形红杆菌中不表达。蓝藻鱼腥藻7120的glnA基因在球形红杆菌中也不表达。未检测到肺炎克雷伯菌ntrA基因从其自身启动子表达的产物以及转座子Tn903卡那霉素抗性基因组成型启动子表达的nifA基因产物的功能活性。文中讨论了这些发现的意义。