Piron-Fraipont C, Duez C, Matagne A, Molitor C, Dusart J, Frère J M, Ghuysen J M
Département de Microbiologie, Université de Liège, Sart Tilman, Belgium.
Biochem J. 1989 Sep 15;262(3):849-54. doi: 10.1042/bj2620849.
By using the promoter-probe plasmid pIJ424, genomic DNA fragments of Actinomadura R39 were shown to have promoter activity in Streptomyces lividans. The same 100-200-copy-number plasmid was used to clone in S. lividans TK24, the gene that encodes the Actinomadura R39 beta-lactamase. Gene cloning resulted in an amplified expression of the beta-lactamase when compared with the amounts of enzyme produced by the original strain (1 mg versus 0.008 mg.litre of culture-1).
通过使用启动子探针质粒pIJ424,已证明马杜拉放线菌R39的基因组DNA片段在淡紫链霉菌中具有启动子活性。使用相同的拷贝数为100 - 200的质粒在淡紫链霉菌TK24中克隆编码马杜拉放线菌R39β-内酰胺酶的基因。与原始菌株产生的酶量相比(每升培养物中1毫克对0.008毫克),基因克隆导致β-内酰胺酶的表达增加。