Murgier M, Gharbi S
Mol Gen Genet. 1982;187(2):316-9. doi: 10.1007/BF00331136.
Strains of Escherichia coli K12 were isolated in which the lac structural genes were fused to the promoter for the aminopeptidasee N structural gene (pepN). Although this enzyme is constitutively produced, the differential rate of synthesis is increased about 4-fold upon phosphate starvation. The pepN-lac fusions were shown to respond to phosphate specific regulatory signals. A plaque forming lambda transducing phage bearing the pepN-lac fusion was isolated. This phage was used to prove genetically the fusion of lac genes to the promoter for the aminopeptidase. These results demonstrate a control at the transcriptional level of aminopeptidase synthesis.
分离出了大肠杆菌K12菌株,其中乳糖操纵子结构基因与氨肽酶N结构基因(pepN)的启动子融合。尽管这种酶是组成型产生的,但在磷酸盐饥饿时,合成的差异速率增加约4倍。已证明pepN-乳糖操纵子融合对磷酸盐特异性调节信号有反应。分离出了携带pepN-乳糖操纵子融合的形成噬菌斑的λ转导噬菌体。该噬菌体被用于从遗传学上证明乳糖基因与氨肽酶启动子的融合。这些结果证明了氨肽酶合成在转录水平上的调控。