Ninfa A J, Ueno-Nishio S, Hunt T P, Robustell B, Magasanik B
J Bacteriol. 1986 Nov;168(2):1002-4. doi: 10.1128/jb.168.2.1002-1004.1986.
We purified the product of glnL (ntrB), NRII, and the product of a mutant glnL allele, NRII2302. In vitro transcription of the nitrogen-regulated promoter glnAp2 by purified components of Escherichia coli required NRII or NRII2302 when the template DNA was linear.
我们纯化了谷氨酰胺合成酶基因L(ntrB)的产物NRII,以及谷氨酰胺合成酶基因L突变等位基因的产物NRII2302。当模板DNA呈线性时,利用大肠杆菌的纯化成分对氮调节启动子谷氨酰胺合成酶基因A2(glnAp2)进行体外转录需要NRII或NRII2302。