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利用转导噬菌体Mu d(Apr lac)在鼠伤寒沙门氏菌LT2中分离ara-lac基因融合体。

Isolation of ara-lac gene fusions in Salmonella typhimurium LT2 by using transducing bacteriophage Mu d (Apr lac).

作者信息

Lee J H, Heffernan L, Wilcox G

出版信息

J Bacteriol. 1980 Sep;143(3):1325-31. doi: 10.1128/jb.143.3.1325-1331.1980.

Abstract

A specialized Mu transducing phage containing a gene encoding ampicillin resistance and the lac structural genes without the lac promotor [Mu d(apr lac)] has been constructed and used to create gene fusions in Escherichia coli (M. J. Cadadaban and S. N. Cohen, Proc. Natl. Acad. Sci. U.S.A. 76:4530--4533, 1979). Transposition of the Mu d(Apr lac) phage to chromosomal sites can result in lac expression being controlled by a chromosomal promoter. We have constructed an Escherichia coli K-12 strain in which the Mu d(Apr lac) phage is integrated into an F factor. The F+::Mu d(Apr lac) was then transferred by conjugation into a Salmonella typhimurium strain that was sensitive to L-arabinose. Strains containing gene fusions were selected as L-arabinose-resistant colonies after partial induction of the phage. Two classes of ara-lac fusion strains were isolated: (i) araC-lac fusions in which the expression of beta-galactosidase synthesis was constitutuve and not inducible by L-arabinose; and ((ii) fusion of the lac genes to the ara structural genes in which the expression of beta-galatosidase synthesis was induced 263-fold by L-arabinose.

摘要

已构建出一种特殊的Mu转导噬菌体,它含有编码氨苄青霉素抗性的基因以及不含lac启动子的lac结构基因[Mu d(apr lac)],并用于在大肠杆菌中创建基因融合体(M. J. 卡达班和S. N. 科恩,《美国国家科学院院刊》76:4530 - 4533, 1979)。Mu d(Apr lac)噬菌体转座到染色体位点可导致lac表达受染色体启动子控制。我们构建了一株大肠杆菌K - 12菌株,其中Mu d(Apr lac)噬菌体整合到了F因子中。然后通过接合将F+::Mu d(Apr lac)转移到对L - 阿拉伯糖敏感的鼠伤寒沙门氏菌菌株中。在对噬菌体进行部分诱导后,将含有基因融合体的菌株选择为抗L - 阿拉伯糖的菌落。分离出了两类ara - lac融合菌株:(i) araC - lac融合体,其中β - 半乳糖苷酶合成的表达是组成型的,且不能被L - 阿拉伯糖诱导;以及(ii) lac基因与ara结构基因的融合体,其中β - 半乳糖苷酶合成的表达被L - 阿拉伯糖诱导了263倍。

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