Deichelbohrer I, Alonso J C, Lüder G, Trautner T A
J Bacteriol. 1985 Jun;162(3):1238-43. doi: 10.1128/jb.162.3.1238-1243.1985.
Any SPP1 DNA restriction fragment cloned into Bacillus subtilis plasmid pC194 or pUB110 increased the transduction frequency of the plasmid by SPP1 100- to 1,000-fold over the transduction level of the plasmid alone. This increment was observed irrespective of whether a fragment contained the SPP1 packaging origin (pac). Furthermore, an SPP1 derivative into whose genome pC194 DNA had been integrated transduced pC194 DNA with a greatly enhanced frequency. Transduction enhancement mediated by DNA-DNA homology between plasmid and SPP1 was independent of the extent of homology (size range analyzed, 0.5 to 3.9 kilobases) and the recombination proficiency of donor or recipient.
任何克隆到枯草芽孢杆菌质粒pC194或pUB110中的SPP1 DNA限制性片段,都使SPP1对该质粒的转导频率比单独质粒的转导水平提高了100至1000倍。无论片段是否包含SPP1包装起始位点(pac),均可观察到这种增加。此外,基因组中整合了pC194 DNA的SPP1衍生物以大大提高的频率转导pC194 DNA。由质粒与SPP1之间的DNA - DNA同源性介导的转导增强与同源性程度(分析的大小范围为0.5至3.9千碱基)以及供体或受体的重组能力无关。