首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >Cloning expression purification and crystallization of dihydrodipicolinate synthase from the grapevine Vitis vinifera
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Cloning expression purification and crystallization of dihydrodipicolinate synthase from the grapevine Vitis vinifera

机译:葡萄Vitis vinifera中的二氢二吡啶甲酸合酶的克隆表达纯化和结晶

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摘要

Dihydrodipicolinate synthase (DHDPS) catalyses the first committed step of the lysine-biosynthesis pathway in bacteria, plants and some fungi. This study describes the cloning, expression, purification and crystallization of DHDPS from the grapevine Vitis vinifera (Vv-DHDPS). Following in-drop cleavage of the hexahistidine tag, cocrystals of Vv-DHDPS with the substrate pyruvate were grown in 0.1 M Bis-Tris propane pH 8.2, 0.2 M sodium bromide, 20%(w/v) PEG 3350. X-ray diffraction data in space group P1 at a resolution of 2.2 Å are presented. Preliminary diffraction data analysis indicated the presence of eight molecules per asymmetric unit (V M = 2.55 Å3 Da−1, 52% solvent content). The pending crystal structure of Vv-DHDPS will provide insight into the molecular evolution in quaternary structure of DHDPS enzymes.
机译:二氢二吡啶甲酸合酶(DHDPS)催化细菌,植物和某些真菌中赖氨酸生物合成途径的第一步。这项研究描述了来自葡萄(Vv-DHDPS)的DHDPS的克隆,表达,纯化和结晶。六组氨酸标签滴入切割后,Vv-DHDPS与底物丙酮酸盐的共晶体在0.1 M Bis-Tris丙烷pH 8.2、0.2 M溴化钠,20%(w / v)PEG 3350中生长。X射线衍射给出了空间群P1中的数据,分辨率为2.2Å。初步衍射数据分析表明,每个不对称单元存在8个分子(V M = 2.55Å 3 Da -1 ,溶剂含量为52%)。 Vv-DHDPS的未决晶体结构将提供DHDPS酶四级结构分子进化的见识。

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