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在大肠杆菌乳糖启动子控制下噬菌体λ阻遏物的过量产生。

Overproduction of phage lambda repressor under control of the lac promotor of Escherichia coli.

作者信息

Gronenborn B

出版信息

Mol Gen Genet. 1976 Nov 17;148(3):243-50. doi: 10.1007/BF00332898.

Abstract

The gene coding for bacteriophage Lambda repressor (cI gene) has been fused to the lac operon of Escherichia coli. In some of the fusions Lambda repressor synthesis can be controlled by the lac operator and promoter. Upon induction of the lac operon the amount of Lambda repressor is increased by a factor of 7 over that found in a single lysogen. In combination with the polarity suppressor suA the induction factor rises to 20. Transducing phages of one fusion were constructed. After thermal induction of this phage the final level of Lambda repressor was enhanced by a factor of 150.

摘要

编码噬菌体λ阻遏物的基因(cI基因)已与大肠杆菌的乳糖操纵子融合。在某些融合中,λ阻遏物的合成可由乳糖操纵基因和启动子控制。诱导乳糖操纵子后,λ阻遏物的量比单个溶原菌中的量增加了7倍。与极性抑制因子suA结合后,诱导因子升至20。构建了一种融合的转导噬菌体。热诱导这种噬菌体后,λ阻遏物的最终水平提高了150倍。

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