Hudson M C, Stewart G C
Gene. 1986;48(1):93-100. doi: 10.1016/0378-1119(86)90355-0.
Promoter-cloning plasmids were constructed and have been used to isolate transcriptionally active DNA fragments from Staphylococcus aureus. The plasmids contain a chloramphenicol acetyltransferase (CAT) gene of Gram-positive (G+) origin which lacks both its promoter and the sequence responsible for CAT inducibility. The ability of S. aureus promoters to direct CAT expression in Escherichia coli and Bacillus subtilis was examined. Two classes of staphylococcal promoter sequences have been obtained. Class I DNA fragments direct CAT expression in S. aureus, B. subtilis, and E. coli, while class II DNA sequences direct CAT expression only in the G+ hosts.
构建了启动子克隆质粒,并用于从金黄色葡萄球菌中分离转录活性DNA片段。这些质粒含有一个革兰氏阳性(G+)来源的氯霉素乙酰转移酶(CAT)基因,该基因既缺乏其启动子,也缺乏负责CAT诱导性的序列。研究了金黄色葡萄球菌启动子在大肠杆菌和枯草芽孢杆菌中指导CAT表达的能力。已获得两类葡萄球菌启动子序列。I类DNA片段可在金黄色葡萄球菌、枯草芽孢杆菌和大肠杆菌中指导CAT表达,而II类DNA序列仅在G+宿主中指导CAT表达。