首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >Crystallization and preliminary X-ray analysis of 5-­keto-d-gluconate reductase from Gluconobacter suboxydans IFO12528 complexed with 5-keto-d-gluconate and NADPH
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Crystallization and preliminary X-ray analysis of 5-­keto-d-gluconate reductase from Gluconobacter suboxydans IFO12528 complexed with 5-keto-d-gluconate and NADPH

机译:与5-酮-d-葡萄糖酸酯和NADPH络合的副氧化葡糖杆菌IFO12528中5 -­-酮-d-葡萄糖酸酯还原酶的结晶和初步X射线分析

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摘要

NADPH-dependent 5-keto-d-gluconate reductase from Gluconobacter suboxy­dans IFO12528 (5KGR) catalyzes oxidoreduction between 5-keto-d-gluconate and d-gluconate with high specificity. 5KGR was expressed in Escherichia coli, purified and crystallized with 5-keto-d-gluconate and NADPH using the sitting-drop vapour-diffusion method at 288 K. A crystal of the 5KGR–NADPH complex was obtained using reservoir solution containing PEG 4000 as a precipitant and diffracted X-rays to 1.75 Å resolution. The crystal of the complex belonged to space group P42212, with unit-cell parameters a = b = 128.6, c = 62.9 Å. A crystal of the 5KGR–NADPH–5-keto-d-gluconate complex was prepared by soaking the 5KGR–NADPH complex crystal in reservoir solution supplemented with 100 mM 5-keto-d-gluconate and 10 mM NADPH for 20 min and diffracted X-rays to 2.26 Å resolution. The crystal of the ternary complex belonged to space group P42212, with unit-cell parameters a = b = 128.7, c = 62.5 Å. Both crystals contained two molecules in the asymmetric unit.
机译:来自亚氧化葡糖杆菌IFO12528(5KGR)的NADPH依赖性5-酮-d-葡萄糖酸还原酶具有高特异性催化5-酮-d-葡萄糖酸和d-葡萄糖酸之间的氧化还原。 5KGR在大肠杆菌中表达,并通过坐滴蒸汽扩散法在288 K下用5-酮-d-葡萄糖酸盐和NADPH纯化和结晶。使用包含PEG 4000的储库溶液获得5KGR-NADPH复合物的晶体。沉淀剂和X射线衍射到1.75Å分辨率。该复合物的晶体属于空间群P42212,单位晶胞参数a = b = 128.6,c = 62.9Å。通过将5KGR–NADPH复合晶体浸泡在补充了100 mM 5-酮-d-葡萄糖酸酯和10 mM NADPH的储液中浸泡20 min并衍射X制成5KGR–NADPH–5-酮-d-葡萄糖酸酯复合物晶体。射线至2.26Å分辨率。三元复合物的晶体属于空间群P42212,单位晶胞参数a = b = 128.7,c = 62.5Å。两个晶体在不对称单元中都包含两个分子。

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