首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >Cloning crystallization and preliminary X-ray diffraction analysis of an intact DNA methyltransferase of a type I restriction–modification enzyme from Vibrio vulnificus
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Cloning crystallization and preliminary X-ray diffraction analysis of an intact DNA methyltransferase of a type I restriction–modification enzyme from Vibrio vulnificus

机译:创伤弧菌I型限制性修饰酶的完整DNA甲基转移酶的克隆结晶和初步X射线衍射分析

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摘要

Independently of the restriction (HsdR) subunit, the specificity (HsdS) and methylation (HsdM) subunits interact with each other, and function as a methyltransferase in type I restriction–modification systems. A single gene that combines the HsdS and HsdM subunits in Vibrio vulnificus YJ016 was expressed and purified. A crystal suitable for X-ray diffraction was obtained from 25%(w/v) polyethylene glycol monomethylether 5000, 0.1 M HEPES pH 8.0, 0.2 M ammonium sulfate at 291 K by hanging-drop vapour diffusion. Diffraction data were collected to a resolution of 2.31 Å using synchrotron radiation. The crystal belonged to the primitive monoclinic space group P21, with unit-cell parameters a = 93.25, b = 133.04, c = 121.49 Å, β = 109.7°. With four molecules in the asymmetric unit, the crystal volume per unit protein weight was 2.61 Å3 Da−1, corresponding to a solvent content of 53%.
机译:独立于限制性(HsdR)亚基,特异性(HsdS)和甲基化(HsdM)亚基彼此相互作用,并在I型限制性修饰系统中充当甲基转移酶。表达和纯化了在创伤弧菌YJ016中结合了HsdS和HsdM亚基的单个基因。通过悬滴气相扩散,在291 K下从25%(w / v)的聚乙二醇单甲醚5000、0.1 M HEPES pH 8.0、0.2 M硫酸铵中获得适合X射线衍射的晶体。使用同步加速器辐射将衍射数据收集到2.31Å的分辨率。该晶体属于原始单斜晶空间群P21,晶胞参数a = 93.25,b = 133.04,c = 121.49Å,β= 109.7°。在不对称单元中有四个分子时,每单位蛋白质重量的晶体体积为2.61Å 3 Da -1 ,对应于53%的溶剂含量。

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