Shpakovskiĭ G V, Khimina M P, Berlin Iu A
Bioorg Khim. 1989 Jul;15(7):997-1000.
Investigating molecular mechanism of illegitimate recombinations in prokaryote we study transducing bacteriophages of the lambda lac series. We have carried out physical mapping of bacteriophage lambda plac9 DNA and, by comparing the obtained results with the data on the structure of lambda DNA and lac operon of E. coli, located the phage-bacterial junction corresponding to the lambda-lac9 abnormal excision and elucidated the nucleotide sequence around the junction. It led to the primary structure of phage and bacterial segments in the lysogenic bacterium which took part in the recombinational act leading to the abnormal excision and lambda lac9 formation. Structural homology of the partners in the lambda plac9 excision proved to be lower than in case of the earlier studied lambda plac5 and lambda plac10 whose excision proceeded regioselectively. Various aspects of the crossover area, including the crossover point's probable position and enzymic systems participating in the abnormal excision, are discussed.
在研究原核生物中非法重组的分子机制时,我们研究了λ lac系列的转导噬菌体。我们对噬菌体λ plac9 DNA进行了物理图谱分析,并通过将所得结果与λ DNA结构和大肠杆菌lac操纵子的数据进行比较,确定了与λ - lac9异常切除相对应的噬菌体 - 细菌连接点,并阐明了连接点周围的核苷酸序列。这导致了溶原性细菌中参与导致异常切除和λ lac9形成的重组行为的噬菌体和细菌片段的一级结构。事实证明,λ plac9切除中伙伴的结构同源性低于早期研究的λ plac5和λ plac10,后者的切除是区域选择性进行的。文中讨论了交叉区域的各个方面,包括交叉点的可能位置以及参与异常切除的酶系统。