Camarena L, Poggio S, García N, Osorio A
Departamento de Biología Molecular, Universidad Nacional Autónoma de México, D.F., Mexico.
FEMS Microbiol Lett. 1998 Oct 1;167(1):51-6. doi: 10.1111/j.1574-6968.1998.tb13206.x.
In this work we show that the nac gene from Escherichia coli is transcriptionally active, and that its expression is dependent on NRI (NtrC) and sigma-54. Northern blot experiments show a monocistronic nac-specific mRNA that is detected when wild-type cells are grown in nitrogen-limiting conditions. Our data also show that in nitrogen-limiting conditions Nac is involved in the transcriptional repression of the gdhA gene (encoding glutamate dehydrogenase) except when L-glutamine is used as the only nitrogen source. Moreover, the high level of GDH activity observed in a nac mutant strain is reduced when a wild-type nac gene is introduced under control of the lac promoter in N-limiting conditions, but not in L-glutamine or N-excess. These results suggest the existence of an additional mechanism responsible for overcoming repression by Nac.
在本研究中,我们发现大肠杆菌的nac基因具有转录活性,其表达依赖于NRI(NtrC)和σ-54。Northern印迹实验显示,当野生型细胞在氮限制条件下生长时,可检测到一种单顺反子nac特异性mRNA。我们的数据还表明,在氮限制条件下,除了以L-谷氨酰胺作为唯一氮源时,Nac参与gdhA基因(编码谷氨酸脱氢酶)的转录抑制。此外,在氮限制条件下,当野生型nac基因在lac启动子控制下导入nac突变株时,观察到的高水平GDH活性会降低,但在L-谷氨酰胺或氮过量条件下则不会。这些结果表明存在一种额外的机制来克服Nac的抑制作用。