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细菌DNA拓扑异构酶I能够使含有单链环的正超螺旋DNA松弛。

Bacterial DNA topoisomerase I can relax positively supercoiled DNA containing a single-stranded loop.

作者信息

Kirkegaard K, Wang J C

出版信息

J Mol Biol. 1985 Oct 5;185(3):625-37. doi: 10.1016/0022-2836(85)90075-0.

Abstract

Using heteroduplex molecules formed from a pair of plasmids, one of which contains a small deletion relative to the other, it is shown that bacterial topoisomerase I can relax a positively supercoiled DNA if a short single-stranded loop is placed in the DNA. This result supports the postulate that the specificity of bacterial DNA topoisomerase I for negatively supercoiled DNA in its relaxation reaction derives from the requirement of a short single-stranded DNA segment in the active enzyme-substrate complex. Nucleolytic and chemical probing of complexes between bacterial DNA topoisomerase I and heteroduplex DNA molecules containing single-stranded loops ranging from 13 to 27 nucleotides in length suggests that the enzyme binds specifically to the region containing a single-stranded loop; the site of DNA cleavage by the topoisomerase appears to lie within the single-stranded loop, with the enzyme interacting with nucleotides on both sides of the point of cleavage.

摘要

利用由一对质粒形成的异源双链分子(其中一个相对于另一个含有小的缺失),研究表明,如果在DNA中放置一个短的单链环,细菌拓扑异构酶I可以使正超螺旋DNA松弛。这一结果支持了这样的假设,即细菌DNA拓扑异构酶I在其松弛反应中对负超螺旋DNA的特异性源于活性酶-底物复合物中短单链DNA片段的需求。对细菌DNA拓扑异构酶I与长度在13至27个核苷酸之间的含单链环的异源双链DNA分子之间的复合物进行核酸酶和化学探测表明,该酶特异性结合到含有单链环的区域;拓扑异构酶切割DNA的位点似乎位于单链环内,酶与切割点两侧的核苷酸相互作用。

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