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Expression purification and crystallization of Chaetomium thermophilum CuZn superoxide dismutase

机译:嗜热死球菌CuZn超氧化物歧化酶的表达纯化和结晶

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摘要

Cu,Zn superoxide dismutase (Cu,ZnSOD) from the thermophilic fungus Chaetomium thermophilum was expressed in Pichia pastoris and purified. Crystals were grown in over 120 conditions but only those produced with 1.4 M sodium potassium phosphate pH 8.2 as precipitant were suitable for structural studies. Data were collected to 1.9 Å resolution at 100 K from a single crystal using a synchrotron-radiation source. The crystals belonged to space group P61/P65, with unit-cell parameters a = 90.2, c = 314.5 Å and eight molecules in the asymmetric unit. Elucidation of the crystal structure will provide insights into the active site of the enzyme and a better understanding of the structure–activity relationship, assembly and thermal stability of Cu,ZnSODs.
机译:嗜热真菌嗜热杆菌(Chaetomium thermophilum)的铜,锌超氧化物歧化酶(Cu,ZnSOD)在毕赤酵母中表达并纯化。晶体在超过120个条件下生长,但只有那些以1.4 M磷酸钠钾(pH 8.2)为沉淀剂的晶体适合进行结构研究。使用同步辐射源从单晶以100 K的分辨率采集到1.9Å的数据。晶体属于空间群P61 / P65,单位晶胞参数a = 90.2,c = 314.5,非对称单元中有8个分子。阐明晶体结构将提供对酶活性位点的见识,并能更好地了解Cu,ZnSODs的结构-活性关系,组装和热稳定性。

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