首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >Expression crystallization and preliminary X-ray crystallographic analysis of d-alanine-d-alanine ligase from OXA-23-producing Acinetobacter baumannii K0420859
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Expression crystallization and preliminary X-ray crystallographic analysis of d-alanine-d-alanine ligase from OXA-23-producing Acinetobacter baumannii K0420859

机译:产生OXA-23的鲍曼不动杆菌K0420859的d-丙氨酸-d-丙氨酸连接酶的表达结晶和初步X射线晶体学分析

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摘要

Acinetobacter baumannii causes bacteraemia, pneumonia, other respiratory-tract and urinary-tract infections in humans. OXA-23 carbapenemase-producing A. baumannii K0420859 (A. baumannii OXA-23) is resistant to carbapenem, a common antibacterial drug. To develop an efficient and novel antibacterial drug against A. baumannii OXA-23, d-alanine-d-alanine ligase, which is essential in bacterial cell-wall synthesis, is of interest. Here, the d-alanine-d-alanine ligase (AbDdl) gene from A. baumannii OXA-23 was cloned and expressed, and the AbDdl protein was purified and crystallized; this enzyme can be used as a novel target for an antibacterial drug against A. baumannii OXA-23. The AbDdl crystal diffracted to a resolution of 2.8 Å and belonged to the orthorhombic space group P212121, with unit-cell parameters a = 113.4, b = 116.7, c = 176.5 Å, a corresponding V M of 2.8 Å3 Da−1 and a solvent content of 56.3%, and six protomers in the asymmetric unit.
机译:鲍曼不动杆菌引起人的菌血症,肺炎,其他呼吸道和泌尿道感染。产生OXA-23碳青霉烯酶的鲍曼不动杆菌K0420859(鲍曼不动杆菌OXA-23)对常见的抗菌药物碳青霉烯耐药。为了开发针对鲍曼不动杆菌OXA-23的有效且新颖的抗菌药物,在细菌细胞壁合成中必不可少的d-丙氨酸-d-丙氨酸连接酶是重要的。在此,克隆并表达了来自鲍曼不动杆菌OXA-23的d-丙氨酸-d-丙氨酸连接酶(AbDdl)基因,并纯化和结晶了AbDdl蛋白。该酶可以用作针对鲍曼不动杆菌OXA-23的抗菌药物的新型靶标。 AbDdl晶体衍射至2.8Å的分辨率,属于正交晶空间群P212121,单位晶胞参数a = 113.4,b = 116.7,c = 176.5Å,相应的VM为2.8Åsup3 Da -1 ,溶剂含量为56.3%,在不对称单元中有六个protomer。

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