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Events following prophage Mu induction.

机译:预言慕事件之后的事件。

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摘要

Escherichia coli strains lysogenic for a thermoinducible Mu prophage (Mu cts62) undergo rapid lysis about 50 min after heat induction. Induction of Mu cts62 apparently causes damage to the host sequences in which Mu is inserted. The normal expression of A, BU, and X genes of Mu is needed for this specific deleterious effect on the prophage-containing host sequences. Mu deoxyribonucleic acid can be shown to reintegrate extensively at different sites on the host genome during the lytic cycle after prophage induction or after infection of sensitive cells by clear-plaque mutants of Mu. We estimate that approximately 10 copies of Mu deoxyribonucleic acid are inserted per chromosome during vegetative growth. The episome rescue method for detecting vegetative Mu deoxyribonucleic acid insertion, in which an episome is transferred from the lytically infected cells to F- receipient cells, can be applied to study Mu integration without requiring the host cells to survive. It also provides an easy system to isolate Mu insertions in transmissible episomes and plasmids.
机译:热诱导的Mu prophage(Mu cts62)的致溶性大肠杆菌菌株在热诱导后约50分钟迅速裂解。 Mu cts62的诱导显然会破坏插入Mu的宿主序列。 Mu的A,BU和X基因的正常表达对于这种对含噬菌体的宿主序列的特定有害作用是必需的。可以证明,Mu脱氧核糖核酸在诱导前体后或在被Mu的空斑突变体感染敏感细胞后的裂解周期中,在宿主基因组的不同位点上广泛整合。我们估计在营养生长期间,每个染色体大约插入10个拷贝的Mu脱氧核糖核酸。用于检测营养性Mu脱氧核糖核酸插入的附加体拯救方法(其中附加体从裂解感染细胞转移到F受体细胞)可用于研究Mu整合,而无需宿主细胞存活。它还提供了一种简便的系统,可将Mu插入可传播的附加体和质粒中。

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