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Construction of Plasmid Cloning Vectors for Lactic Streptococci Which Also Replicate in Bacillus subtilis and Escherichia coli

机译:乳酸链球菌也可在枯草芽孢杆菌和大肠杆菌中复制的质粒克隆载体的构建

摘要

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.
机译:用来自pC194的氯霉素抗性(Cmr)基因在遗传上标记了隐秘的克雷莫氏链球菌Wg2质粒pWV01(1.5兆道尔顿)。重组质粒(pGK1,2.4兆道尔顿)在枯草芽孢杆菌中复制并表达了Cmr。通过插入来自pE194 cop-6的红霉素抗性(Emr)基因,从该质粒构建了插入失活载体。该质粒(pGK12,2.9兆道尔顿)在Emr基因中包含一个独特的BclI位点,在两个抗性基因之外均包含一个独特的ClaI和HpaII位点。它以约5的拷贝数稳定地保持在枯草芽孢杆菌中。pGK12还将大肠杆菌感受态细胞转化为Cmr和Emr。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。在该宿主中,两种抗性基因均被表达。 pGK12稳定地保持在乳酸链球菌中,拷贝数为3。

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