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通过质粒载体在大肠杆菌中繁殖来自酿酒酵母线粒体DNA的限制性片段。

Propagation of restriction fragments from the mitochondrial DNA of Saccharomyces cerevisiae in E. coli by means of plasmid vectors.

作者信息

Berg P E, Lewin A, Christianson T, Rabinowitz M

出版信息

Nucleic Acids Res. 1979;6(6):2133-50. doi: 10.1093/nar/6.6.2133.

Abstract

Some of the EcoRI fragments of yeast (Saccharomyces cerevisiae) mitochondrial DNA were cloned into E. coli using plasmid pMB9. The five smallest fragments in molecular weight appeared to be preferentially retained by E coli; partial fragments derived from larger mitochondrial DNA fragments were also found. One of the fragments, R7 (2.4 kb), may contain the OII gene. Cloned R7 DNA was stable under a variety of growth conditions, but showed some changes in molecular weight after transfer to different E. coli strains. Fragment R7 is transcribed in minicells, producing RNA that hybridizes specifically to mitochondrial DNA. Both DNA strands are transcribed, in contrast to the asymmetric transcription found in mitochondria. No new polypeptides were observed in minicells containing cloned fragment 7.

摘要

利用质粒pMB9将酵母(酿酒酵母)线粒体DNA的一些EcoRI片段克隆到大肠杆菌中。分子量最小的五个片段似乎被大肠杆菌优先保留;还发现了源自较大线粒体DNA片段的部分片段。其中一个片段R7(2.4 kb)可能包含OII基因。克隆的R7 DNA在各种生长条件下都很稳定,但转移到不同的大肠杆菌菌株后分子量出现了一些变化。片段R7在小细胞中被转录,产生与线粒体DNA特异性杂交的RNA。与线粒体中发现的不对称转录不同,两条DNA链都被转录。在含有克隆片段7的小细胞中未观察到新的多肽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98e2/327841/dcd8bbdc8883/nar00447-0103-a.jpg

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