Keen N T, Tamaki S, Kobayashi D, Trollinger D
Department of Plant Pathology, University of California, Riverside 92521.
Gene. 1988 Oct 15;70(1):191-7. doi: 10.1016/0378-1119(88)90117-5.
Improved broad-host-range plasmid vectors were constructed based on existing plasmids RSF1010 and RK404. The new plasmids pDSK509, pDSK519, and pRK415, have several additional cloning sites and improved antibiotic-resistance genes which facilitate subcloning and mobilization into various Gram-negative bacteria. Several new polylinker sites were added to the Escherichia coli plasmids pUC118 and pUC119, resulting in the new plasmids, pUC128 and pUC129. These plasmids facilitate the transfer of cloned DNA fragments to the broad-host-range vectors. Finally, the broad-host-range cosmid cloning vector pLAFR3 was improved by the addition of a double cos casette to generate the new plasmid, pLAFR5. This latter cosmid simplifies vector preparation and has permitted the rapid cloning of genomic DNA fragments generated with Sau3A. The resulting clones may be introduced into other Gram-negative bacteria by conjugation.
基于现有的质粒RSF1010和RK404构建了改良的广宿主范围质粒载体。新的质粒pDSK509、pDSK519和pRK415具有多个额外的克隆位点和改良的抗生素抗性基因,这有助于亚克隆以及向各种革兰氏阴性菌中转移。在大肠杆菌质粒pUC118和pUC119中添加了几个新的多克隆位点,从而产生了新的质粒pUC128和pUC129。这些质粒便于将克隆的DNA片段转移到广宿主范围载体中。最后,通过添加双黏粒盒对广宿主范围黏粒克隆载体pLAFR3进行了改良,从而产生了新的质粒pLAFR5。后一种黏粒简化了载体制备,并允许快速克隆用Sau3A产生的基因组DNA片段。所得克隆可通过接合作用导入其他革兰氏阴性菌中。