Greenfield L, Boone T, Wilcox G
Proc Natl Acad Sci U S A. 1978 Oct;75(10):4724-8. doi: 10.1073/pnas.75.10.4724.
The L-arabinose operon in Escherichia coli is a model system for the study of the control of gene expression. Maximal expression of the araBAD operon requires two positive control components: the araC protein-L-arabinose complex and the cyclic AMP receptor protein-cyclic AMP complex. Both araC protein and cyclic AMP receptor protein are required for the initiation of transcription of araBAD mRNA. We have used the plasmid pBR322 as a vector for cloning DNA fragments that contain the araBAD promoter. The cloned ara fragments were identified by both physical and genetic tests. A restriction map was constructed and the DNA sequence of the promoter was determined. The promoter contains a site that is similar to the RNA polymerase recognition sites in the galactose and lactose operons. It also contains a region similar to the known cyclic AMP receptor protein binding sites in the galactose and lactose operons.
大肠杆菌中的L-阿拉伯糖操纵子是用于研究基因表达调控的模型系统。araBAD操纵子的最大表达需要两个正调控元件:araC蛋白-L-阿拉伯糖复合物和环腺苷酸受体蛋白-环腺苷酸复合物。araC蛋白和环腺苷酸受体蛋白都是启动araBAD mRNA转录所必需的。我们使用质粒pBR322作为载体来克隆含有araBAD启动子的DNA片段。通过物理和遗传学测试鉴定了克隆的ara片段。构建了限制酶切图谱并确定了启动子的DNA序列。该启动子包含一个与半乳糖和乳糖操纵子中RNA聚合酶识别位点相似的位点。它还包含一个与半乳糖和乳糖操纵子中已知的环腺苷酸受体蛋白结合位点相似的区域。