Kok J, van der Vossen J M, Venema G
Appl Environ Microbiol. 1984 Oct;48(4):726-31. doi: 10.1128/aem.48.4.726-731.1984.
The cryptic Streptococcus cremoris Wg2 plasmid pWV01 (1.5 megadaltons) was genetically marked with the chloramphenicol resistance (Cmr) gene from pC194. The recombinant plasmid (pGK1, 2.4 megadaltons) replicated and expressed Cmr in Bacillus subtilis. From this plasmid an insertion-inactivation vector was constructed by inserting the erythromycin resistance (Emr) gene from pE194 cop-6. This plasmid (pGK12, 2.9 megadaltons) contained a unique BclI site in the Emr gene and unique ClaI and HpaII sites outside both resistance genes. It was stably maintained in B. subtilis at a copy number of approximately 5. pGK12 also transformed Escherichia coli competent cells to Cmr and Emr. The copy number in E. coli was about 60. Moreover, pGK12 transformed protoplasts of Streptococcus lactis. In this host both resistance genes are expressed. pGK12 is stably maintained in S. lactis at a copy number of 3.
隐秘的嗜热链球菌Wg2质粒pWV01(1.5兆道尔顿)用来自pC194的氯霉素抗性(Cmr)基因进行了遗传标记。重组质粒(pGK1,2.4兆道尔顿)在枯草芽孢杆菌中复制并表达Cmr。从该质粒构建了一个插入失活载体,方法是插入来自pE194 cop - 6的红霉素抗性(Emr)基因。该质粒(pGK12,2.9兆道尔顿)在Emr基因中含有一个独特的BclI位点,在两个抗性基因之外含有独特的ClaI和HpaII位点。它在枯草芽孢杆菌中以大约5的拷贝数稳定维持。pGK12还将大肠杆菌感受态细胞转化为对氯霉素和红霉素抗性。在大肠杆菌中的拷贝数约为60。此外,pGK12转化了乳酸链球菌的原生质体。在这个宿主中,两个抗性基因都表达。pGK12在乳酸链球菌中以3的拷贝数稳定维持。