首页> 美国卫生研究院文献>Nucleic Acids Research >Restoration of ligase activity in E. coli K12 lig ts7 strain by bacteriophage Mu and cloning of a DNA fragment harbouring the Mu lig gene.
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Restoration of ligase activity in E. coli K12 lig ts7 strain by bacteriophage Mu and cloning of a DNA fragment harbouring the Mu lig gene.

机译:通过噬菌体Mu恢复大肠杆菌K12 lig ts7菌株中的连接酶活性并克隆具有Mulig基因的DNA片段。

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摘要

Restoration of ligase activity has been observed in E. coli K12 ligts7 strain lysogenic for Mu, in presence as well in absence of lysogenic immunity. This restoration consist in phenotypic reversal of temperature sensitivity of E. coli ligts7 which also regain the ability to sustain the complete growth cycle of T4 lig-phages. It is possible to put under the control of the gal operon the expression of the viral gene responsible for the restoration effect. This new gene of Mu has been named 'lig'. A 5 kb fragment responsible for the reported effects and localized between genes gam and lys of Mu genome has been cloned in pBR322. This recombinant plasmid used for transforming ligts7 strain restores in it normal behaviour for ligation of Okazaki pieces.
机译:在存在和不存在溶原性免疫的情况下,在对Mu具有致溶性的大肠杆菌K12 ligts7菌株中,观察到连接酶活性的恢复。这种恢复包括大肠杆菌ligts7温度敏感性的表型逆转,这也恢复了维持T4噬菌体完整生长周期的能力。可以在gal操纵子的控制下使负责恢复作用的病毒基因表达。 Mu的这个新基因被命名为“ lig”。已将负责报道效应并位于Mu基因组的基因gam和lys之间的5 kb片段克隆到pBR322中。用于转化ligts7菌株的重组质粒恢复了冈崎片段连接的正常行为。

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