Gamper M, Haas D
Mikrobiologisches Institut, Eidgenössische Technische Hochschule, Zürich, Switzerland.
Gene. 1993 Jul 15;129(1):119-22. doi: 10.1016/0378-1119(93)90706-9.
In Pseudomonas aeruginosa, arginine catabolism via the arginine deiminase pathway depends on the anaerobically inducible arcDABC operon, whose expression is further modulated by mRNA processing. Fusion of the cloned arc operon to an external tac promoter did not alter the processing pattern in P. aeruginosa and allowed heterologous expression in Escherichia coli. Processing within a specific region of the arcD mRNA was similar in P. aeruginosa and in E. coli. In E. coli, a conditional temperature-sensitive (ts) mutation in the gene specifying RNase E prevented cleavage of the arc mRNA at the non-permissive temperature, whereas mutations in the genes encoding RNase III or RNase P had no effect. We therefore speculate that in P. aeruginosa, an RNase E-like enzyme exists which is involved in the specific processing of the arc mRNA.
在铜绿假单胞菌中,通过精氨酸脱亚氨酶途径进行的精氨酸分解代谢依赖于厌氧诱导的arcDABC操纵子,其表达通过mRNA加工进一步调节。将克隆的arc操纵子与外部tac启动子融合不会改变铜绿假单胞菌中的加工模式,并允许在大肠杆菌中进行异源表达。arcD mRNA特定区域内的加工在铜绿假单胞菌和大肠杆菌中相似。在大肠杆菌中,指定核糖核酸酶E的基因中的条件性温度敏感(ts)突变在非允许温度下阻止了arc mRNA的切割,而编码核糖核酸酶III或核糖核酸酶P的基因中的突变没有影响。因此,我们推测在铜绿假单胞菌中存在一种类似核糖核酸酶E的酶,它参与arc mRNA的特异性加工。