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首页> 外文期刊>Nucleic acids research >Propagation of restriction fragments from the mitochondrial DNA of Saccharomyces cerevisiae in E coli by means of plasmid vectors
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Propagation of restriction fragments from the mitochondrial DNA of Saccharomyces cerevisiae in E coli by means of plasmid vectors

机译:通过质粒载体从啤酒酵母线粒体DNA中扩增限制性片段

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摘要

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 0II 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.
机译:使用质粒pMB9将酵母线粒体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优先被大肠杆菌保留;还发现了来自较大线粒体DNA片段的部分片段。其中一个片段R7(2.4 kb)可能包含0 II 基因。克隆的R7 DNA在多种生长条件下均稳定,但在转移至不同的大肠杆菌菌株后,分子量显示出一些变化。片段R7在小细胞中转录,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相反,两条DNA链均被转录。在含有克隆片段7的小细胞中未观察到新的多肽。

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