Tuli R, Fisher R, Haselkorn R
Gene. 1982 Jul-Aug;19(1):109-16. doi: 10.1016/0378-1119(82)90195-0.
Regulation of the synthesis of glutamine synthetase and of the arginine and glutamine transport systems (Ntr phenotype) in Salmonella have been shown to require two regulatory genes on the C-terminal side of the glnA gene (McFarland et al., 1981). We have cloned a HindIII-EcoRI DNA fragment from Escherichia coli coding for analogous properties with respect to the Ntr phenotype in E. coli. A plasmid containing this E. coli DNA fragment joined to another fragment carrying a cyanobacterial glnA gene (but no functional regulatory genes) was introduced into a Klebsiella pneumoniae mutant with a Gln-Ntr- phenotype, i.e., which could not derepress nitrogenase. The cyanobacterial gene made the Klebsiella strain Gln+ and the E. coli DNA fragment made the strain Ntr+, including the ability to derepress nitrogenase fully. Thus the products of the glnA-linked ntr genes of E. coli can regulate expression of the Ntr-dependent genes of Klebsiella.
已证明,沙门氏菌中谷氨酰胺合成酶以及精氨酸和谷氨酰胺转运系统(Ntr表型)的合成调控需要glnA基因C端的两个调控基因(麦克法兰等人,1981年)。我们从大肠杆菌中克隆了一个HindIII-EcoRI DNA片段,该片段编码与大肠杆菌Ntr表型类似的特性。将一个含有此大肠杆菌DNA片段并与携带蓝藻glnA基因(但无功能性调控基因)的另一个片段相连的质粒导入具有Gln-Ntr-表型的肺炎克雷伯菌突变体中,即该突变体无法解除对固氮酶的阻遏。蓝藻基因使肺炎克雷伯菌菌株变为Gln+,而大肠杆菌DNA片段使该菌株变为Ntr+,包括完全解除对固氮酶阻遏的能力。因此,大肠杆菌glnA连锁的ntr基因产物可以调控肺炎克雷伯菌Ntr依赖基因的表达。