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编码DNA拓扑异构酶I的topA基因的克隆及大肠杆菌cysB-topA-trp区域的物理图谱绘制。

Cloning of the gene topA encoding for DNA topoisomerase I and the physical mapping of the cysB-topA-trp region of Escherichia coli.

作者信息

Wang J C, Becherer K

出版信息

Nucleic Acids Res. 1983 Mar 25;11(6):1773-90. doi: 10.1093/nar/11.6.1773.

Abstract

The gene topA of Escherichia coli that encodes for DNA topoisomerase I has been cloned by a combination of genetic and radioimmunal screening. The gene has been mapped to be within a 3.4 Kb segment of the bacterial genome. The intracellular level of the enzyme in strains harboring extrachromosomal copies of topA gene increases with increasing copy number of the gene and the introduction of extrachromosomal copies of the topA gene truncated at its 3' side into a topA strain of E. coli does not significantly influence the expression of the chromosomal copy of topA. These results suggest that the expression of topA is not tightly regulated. Strains in which DNA topoisomerase I is overproduced grow significantly slower in broth and give smaller size colonies on agar plates. Physical mapping of a 20 Kb region containing cysB; topA and trp has also been carried out with a number of restriction enzymes; topA is found to be immediately adjacent to cysB and is separated from trp by a 7 Kb segment where no known gene resides.

摘要

通过遗传筛选和放射免疫筛选相结合的方法,克隆了编码大肠杆菌DNA拓扑异构酶I的基因topA。该基因被定位在细菌基因组的一个3.4 Kb片段内。携带topA基因染色体外拷贝的菌株中,该酶的细胞内水平随着基因拷贝数的增加而增加,并且将3'端截短的topA基因的染色体外拷贝导入大肠杆菌的topA菌株中,对topA染色体拷贝的表达没有显著影响。这些结果表明,topA的表达不受严格调控。DNA拓扑异构酶I过量产生的菌株在肉汤中生长明显较慢,在琼脂平板上形成的菌落较小。还使用了多种限制酶对包含cysB、topA和trp的20 Kb区域进行了物理图谱分析;发现topA紧邻cysB,与trp之间被一个7 Kb的片段隔开,该片段中没有已知基因。

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