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腺病毒中期系统:通过Tn7介导的转座在大肠杆菌中产生重组腺病毒。

The admid system: generation of recombinant adenoviruses by Tn7-mediated transposition in E. coli.

作者信息

Richards C A, Brown C E, Cogswell J P, Weiner M P

机构信息

Glaxo Wellcome, Research Triangle Park, NC, USA.

出版信息

Biotechniques. 2000 Jul;29(1):146-54. doi: 10.2144/00291rr01.

Abstract

A new system has been developed for generating recombinant adenoviruses by Tn7-mediated transposition in E. coli. Low copy number E. coli plasmids containing a full-length adenoviral genome with lacZattTn7 replacing E1 have been constructed. The adenovirus plasmid or admid, as well as high copy number progenitors, were stably maintained in E. coli strain DH10B. Several transfer vectors containing a mammalian expression cassette flanked by Tn7R and Tn7L were used as donors to transpose the mini-Tn7 into the E1 region of the adenoviral genome. Transposed recombinant admids are readily identified by their beta-galactosidase phenotype. Transfection of admid DNA into producer cells resulted in the efficient production of infectious adenovirus. This easy-to-use, efficient system generates pure, clonal stocks of recombinant adenovirus without successive rounds of plaque purification.

摘要

已开发出一种新系统,用于通过Tn7介导的转座在大肠杆菌中产生重组腺病毒。构建了低拷贝数的大肠杆菌质粒,其含有全长腺病毒基因组,其中lacZattTn7取代了E1区。腺病毒质粒或腺病毒中期质粒以及高拷贝数前体在大肠杆菌DH10B菌株中稳定维持。几种含有由Tn7R和Tn7L侧翼的哺乳动物表达盒的转移载体用作供体,将mini-Tn7转座到腺病毒基因组的E1区。通过其β-半乳糖苷酶表型很容易鉴定转座的重组腺病毒中期质粒。将腺病毒中期质粒DNA转染到生产细胞中可高效产生感染性腺病毒。这种易于使用的高效系统可产生纯的、克隆的重组腺病毒株,无需连续进行噬斑纯化。

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