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利用重组DNA技术分析支原体基因组。

Analysis of the mycoplasma genome by recombinant DNA technology.

作者信息

Christiansen C, Frydenberg J, Christiansen G, Andersen H, Hedegaard L

出版信息

Isr J Med Sci. 1984 Sep;20(9):781-4.

PMID:6392184
Abstract

A library of DNA fragments from Mycoplasma sp. strain PG50 has been made in the vector pBR325. Analysis in Escherichia coli minicells of randomly picked clones from this library demonstrated that many plasmids can promote synthesis of mycoplasma protein in the E. coli genetic background. Screening with labeled rRNA identified plasmids with sequences from the beginning of the rRNA cistron to about two-thirds within the gene for 23S rRNA. Use of these plasmids as probes allowed an accurate determination of the number of RNA cistrons as two, and demonstrated that the cistrons are more than 20 kbp apart. The DNA sequence of 16S rRNA and the surrounding control regions has been determined.

摘要

已经构建了来自支原体菌株PG50的DNA片段文库,载体为pBR325。对该文库中随机挑选的克隆在大肠杆菌微小细胞中进行分析表明,许多质粒能够在大肠杆菌遗传背景下促进支原体蛋白的合成。用标记的rRNA进行筛选,鉴定出了含有从rRNA顺反子起始序列到23S rRNA基因内约三分之二序列的质粒。使用这些质粒作为探针能够准确确定RNA顺反子的数量为两个,并表明这两个顺反子相距超过20千碱基对。已经测定了16S rRNA及其周围调控区域的DNA序列。

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