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McrBC切割对识别元件之间距离的依赖性。

Dependence of McrBC cleavage on distance between recognition elements.

作者信息

Stewart F J, Raleigh E A

机构信息

New England Biolabs, Beverly, MA 01915, USA.

出版信息

Biol Chem. 1998 Apr-May;379(4-5):611-6.

PMID:9628366
Abstract

DNA cleavage by the modification-dependent restriction enzyme McrBC requires the presence of two suitably modified recognition elements appropriately spaced in the substrate. To characterize the spacing requirement in more detail, we have constructed a plasmid with a single McrBC cleavage site, in which the distance between recognition elements could be systematically varied while preserving the local sequence surrounding the recognition elements. Optimal separation between elements was 55-103 basepairs, with detectable cleavage observed at spacing of 32 bp to 2 kb; no cleavage was seen with spacing of 22 bp or less or with 3 kb between elements. Changing the spacing by 4 basepairs within the optimal range had little effect on the efficiency of cleavage, suggesting that the recognition elements need not lie on the same face of the DNA helix.

摘要

依赖修饰的限制酶McrBC切割DNA需要在底物中存在两个适当修饰的识别元件,并以适当的间距排列。为了更详细地描述间距要求,我们构建了一个带有单个McrBC切割位点的质粒,其中识别元件之间的距离可以系统地变化,同时保留识别元件周围的局部序列。元件之间的最佳间隔为55 - 103个碱基对,在32 bp至2 kb的间距处可观察到可检测的切割;元件之间间距为22 bp或更小或为3 kb时未观察到切割。在最佳范围内将间距改变4个碱基对,对切割效率影响不大,这表明识别元件不一定位于DNA螺旋的同一面上。

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