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将lac基因与大肠杆菌K-12胞嘧啶脱氨酶基因的启动子融合。

Fusion of the lac genes to the promotor for the cytidine deaminase gene of Escherichia coli K-12.

作者信息

Josephsen J, Hammer-Jespersen K

出版信息

Mol Gen Genet. 1981;182(1):154-8. doi: 10.1007/BF00422783.

Abstract

Phage Mu has been inserted into the structural gene for cytidine deaminase (cdd). By the use of phage lambda (lac, Mu) the promoter for the cdd gene has been fused to lacZ. In these strains lacZ expression is regulated by the cytR repressor protein and is therefore induced by cytidine. The fusion strains were used for the isolation of cddo mutants. Plaque forming lambda phages carrying the different cdd-lacZ fusions were isolated. Studies of the cdd-Mu strains showed that the cdd gene is transcribed clockwise with respect to the Escherichia coli map.

摘要

噬菌体Mu已插入胞苷脱氨酶(cdd)的结构基因中。通过使用噬菌体λ(lac,Mu),cdd基因的启动子已与lacZ融合。在这些菌株中,lacZ的表达受cytR阻遏蛋白调控,因此可被胞苷诱导。这些融合菌株被用于分离cddo突变体。分离出了携带不同cdd-lacZ融合体的噬菌斑形成λ噬菌体。对cdd-Mu菌株的研究表明,相对于大肠杆菌图谱,cdd基因是顺时针转录的。

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