Duran R, Chion C K, Arnaud A, Galzy P
Chaire de Microbiologie Industrielle et de Génétique des Microorganismes, Ecole Nationale Supérieure Agronomique, Montpellier, France.
Zentralbl Mikrobiol. 1992 Nov;147(8):499-502.
Promoter sequences recognized by Escherichia coli RNA polymerase were isolated from Brevibacterium sp. R312, a coryneform strain producing nitrile hydratase and amidase. Ten Escherichia coli clones containing promoter sequences were selected for their ability to grow with chloramphenicol concentrations of up to 1500 micrograms/ml. The strength of these promoter sequences was determined. We carried out a preliminary study of the strongest promoter having a chloramphenicol acetyl-transferase/beta-lactamase activities ratio of 18.4.
从短杆菌属R312(一种产腈水合酶和酰胺酶的棒状菌株)中分离出了能被大肠杆菌RNA聚合酶识别的启动子序列。选择了十个含有启动子序列的大肠杆菌克隆,因其能在高达1500微克/毫升氯霉素浓度下生长。测定了这些启动子序列的强度。我们对氯霉素乙酰转移酶/β-内酰胺酶活性比为18.4的最强启动子进行了初步研究。