首页> 美国卫生研究院文献>Nucleic Acids Research >Does the specific recognition of DNA by the restriction endonuclease EcoRI involve a linear diffusion step? Investigation of the processivity of the EcoRI endonuclease.
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Does the specific recognition of DNA by the restriction endonuclease EcoRI involve a linear diffusion step? Investigation of the processivity of the EcoRI endonuclease.

机译:限制性核酸内切酶EcoRI对DNA的特异性识别是否涉及线性扩散步骤?研究EcoRI核酸内切酶的生产力。

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摘要

The time course of the EcoRI endonuclease catalysed cleavage of three substrates, two plasmid DNAs and one oligonucleotide, each with two EcoRI sites, was measured. The two plasmid DNAs with the EcoRI sites 318 and 96 base pairs apart are cut in a distributive fashion, while the oligonucleotide with the EcoRI sites 8 base pairs apart is cut in a partially processive manner. It is concluded that a linear diffusion of the EcoRI endonuclease on its substrate across long stretches of DNA is not likely to be operative during the recognition process. Microscopic dissociation-reassociation processes, however, increase the probability of the enzyme to attack further sites located in the immediate vicinity of a given site.
机译:测量了EcoRI核酸内切酶催化的三种底物,两个质粒DNA和一个寡核苷酸的裂解的时间进程,每个底物具有两个EcoRI位点。以分布方式切割具有EcoRI位点318和96个碱基对的两个质粒DNA,而以部分加工方式切割具有EcoRI位点8个碱基对的寡核苷酸。结论是,在识别过程中,EcoRI核酸内切酶在其底物上跨长链DNA的线性扩散不太可能起作用。然而,微观解离-重结合过程增加了酶攻击位于给定位点附近的其他位点的可能性。

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