首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Filamentous coliphage M13 as a cloning vehicle: insertion of a HindII fragment of the lac regulatory region in M13 replicative form in vitro.
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Filamentous coliphage M13 as a cloning vehicle: insertion of a HindII fragment of the lac regulatory region in M13 replicative form in vitro.

机译:丝状噬菌体M13作为克隆媒介:体外以M13复制形式插入lac调控区的HindII片段。

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摘要

A HindII restriction fragment comprising the Escherichia coli lac regulatory region and the genetic information for the alpha peptide of beta-galactosidase (beta-D-galactosidegalactohydrolase, EC. 3.2.1.23) has been inserted into 1 of the 10 Bsu I cleavage sites of M13 by blunt end ligation. A stable hybrid phage was isolated and identified by its ability to complement the lac alpha function. Further characterization of the hybrid phage includes retransformation studies, agarose gel electrophoresis, DNA-DNA hybridization, and heteroduplex mapping. The insertion point has been localized at 0.083 map unit on thewild-type circular map-i.e., within the intergenic region. The results prove that part of the intergenic region is nonessential and that the phage can be used as a cloning vehicle.
机译:包含大肠杆菌lac调控区和β-半乳糖苷酶α肽的遗传信息(β-D-半乳糖苷半乳糖水解酶,EC.3.2.1.23)的HindII限制性片段已插入M13的10个Bsu I切割位点之一。通过钝端结扎。分离出稳定的杂合噬菌体,并通过其补充lacα功能的能力进行鉴定。杂交噬菌体的进一步表征包括重新转化研究,琼脂糖凝胶电泳,DNA-DNA杂交和异源双链作图。插入点已定位在野生型圆形图谱上的0.083个图谱单元处,即在基因间区域内。结果证明部分基因间区域是非必需的,并且噬菌体可用作克隆载体。

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