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首页> 外文期刊>Nucleic acids research >Does the specific recongnition 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 recongnition 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? EcoRI核酸内切酶的生产力研究

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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 3 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。 EcoRI位点分别为318和96个碱基对的两个质粒DNA均以分布方式被切割,而EcoRI位点为3个碱基对的寡核苷酸以部分加工的方式被切割。结论是EcoRI的线性扩散跨越长链DNA的底物上的核酸内切酶在识别过程中不太可能起作用。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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