Dhaese P, Dobbelaere M R, Van Montagu M
Mol Gen Genet. 1985;200(3):490-2. doi: 10.1007/BF00425736.
Two different PstI fragments of temperate phage phi 105 DNA are shown to confer superinfection immunity upon Bacillus subtilis when inserted into the multicopy cloning vector pE194 cop-6. The 2.3 kb PstI fragment I is located almost entirely within EcoRI fragment F and encompasses a region previously known to encode a repressor. The other fragment, PstI-E (4.3 kb) maps inside the EcoRI-B fragment, and allows an explanation of the clear-plaque phenotype of the deletion mutant phi 105DII:6c. The two regions can be distinguished functionally, since only the PstI fragment I product interacts with a specific phi 105 promoter-operator site.
当温和噬菌体φ105 DNA的两个不同的PstI片段插入多拷贝克隆载体pE194 cop-6时,它们可赋予枯草芽孢杆菌超感染免疫性。2.3 kb的PstI片段I几乎完全位于EcoRI片段F内,包含一个先前已知编码阻遏物的区域。另一个片段PstI-E(4.3 kb)定位于EcoRI-B片段内,这可以解释缺失突变体φ105DII:6c的清晰噬菌斑表型。这两个区域在功能上可以区分,因为只有PstI片段I的产物与特定的φ105启动子-操纵子位点相互作用。