Müller J, Malke H
Academy of Sciences of the G.D.R., Central Institute of Microbiology and Experimental Therapy, Jena.
FEMS Microbiol Lett. 1990 Oct;60(1-2):75-8. doi: 10.1016/0378-1097(90)90348-t.
The erythromycin resistance plasmid pSM752 carrying the cloned streptokinase gene, skc, was introduced by protoplast transformation into Streptococcus equisimilis H46A from which skc was originally cloned. Cells transiently supporting the replication of pSM752 gave rise to an erythromycin-resistant clone designated H46SM which was plasmid free and produced streptokinase at levels approximately twice as high as the wild type. Southern hybridization of total cell DNA with an skc-containing probe provided evidence for the duplication of the skc gene in the H46SM chromosome. The results, which have some bearing on industrial streptokinase production, can be best explained by a single cross-over event between the chromosome and the plasmid in the region of shared homology leading to the integration of pSM752 in a Campbell-like manner.
携带克隆的链激酶基因skc的红霉素抗性质粒pSM752通过原生质体转化被导入到最初从中克隆出skc的类马链球菌H46A中。短暂支持pSM752复制的细胞产生了一个名为H46SM的红霉素抗性克隆,该克隆不含质粒,产生链激酶的水平约为野生型的两倍。用含skc的探针与总细胞DNA进行Southern杂交,为H46SM染色体中skc基因的复制提供了证据。这些结果与工业链激酶生产有一定关系,最合理的解释是在同源区域染色体与质粒之间发生了单交换事件,导致pSM752以类似坎贝尔的方式整合。