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将真核生物5S RNA和组蛋白基因整合到噬菌体λ受体中。

Integration of eukaryotic genes for 5S RNA and histone proteins into a phage lambda receptor.

作者信息

Clarkson S G, Smith H O, Schaffner W, Gross K W, Birnstiel M L

出版信息

Nucleic Acids Res. 1976 Oct;3(10):2617-32. doi: 10.1093/nar/3.10.2617.

Abstract

Highly purified HindIII restriction fragments of Xenopus laevis 5S DNA and of Psammechinus miliaris histone DNA have been covalently inserted into a derivative of phage lambda. This phage, genetically constructed by Murray et al. (1), contains only a single target for HindIII in the cI gene. Viable hybrid molecules were detected as clear plaque-forming phage after transfection of E. coli, the vast majority of which were shown by hybridization to be recombinants of the desired type. The lambdaSam7 mutation has been introduced into one hybrid phage containing histone DNA, thereby substantially increasing the yield of recombinant DNA.

摘要

非洲爪蟾5S DNA和砂海胆组蛋白DNA的高度纯化的HindIII限制性片段已被共价插入噬菌体λ的一个衍生物中。这种噬菌体是由默里等人(1)通过基因构建的,在cI基因中仅含有一个HindIII的靶位点。在大肠杆菌转染后,可检测到有活力的杂交分子,它们表现为清亮噬菌斑形成噬菌体,通过杂交表明其中绝大多数是所需类型的重组体。已将λSam7突变引入一个含有组蛋白DNA的杂交噬菌体中,从而显著提高了重组DNA的产量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7885/343117/9dbe4b3c64c1/nar00495-0221-a.jpg

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