Lydiate D J, Malpartida F, Hopwood D A
Gene. 1985;35(3):223-35. doi: 10.1016/0378-1119(85)90001-0.
Detailed restriction maps of the plasmid SCP2* and its deletion derivative pSCP103 were constructed. DNA fragments carrying hygromycin (Hyg), thiostrepton (Thio) or viomycin-resistance (VioR) determinants were inserted into pSCP103, and various segments were deleted from the resulting plasmids. Changes in plasmid phenotypes associated with these insertions and deletions allowed the localisation and characterisation of plasmid replication, stability, transfer and fertility functions. Several useful cloning vectors were constructed. They are able to maintain large (greater than 30 kb) DNA inserts, with stable inheritance at a low copy number (1-2 per chromosome) and without structural rearrangements, in Streptomyces hosts. The vectors have a broad host range in the genus Streptomyces. One of them (pIJ903) is a shuttle vector for Streptomyces and Escherichia coli.
构建了质粒SCP2*及其缺失衍生物pSCP103的详细限制酶图谱。将携带潮霉素(Hyg)、硫链丝菌素(Thio)或紫霉素抗性(VioR)决定簇的DNA片段插入pSCP103,并从所得质粒中缺失了各个片段。与这些插入和缺失相关的质粒表型变化使得能够定位和表征质粒的复制、稳定性、转移和育性功能。构建了几种有用的克隆载体。它们能够在链霉菌宿主中维持大片段(大于30 kb)的DNA插入片段,以低拷贝数(每条染色体1 - 2个)稳定遗传且无结构重排。这些载体在链霉菌属中具有广泛的宿主范围。其中之一(pIJ903)是用于链霉菌和大肠杆菌的穿梭载体。