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分子内 NH···O 氢键对 Mg²⁺依赖的磷酸酶模型水解活性的调控。

Regulation of the hydrolytic activity of Mg²⁺-dependent phosphatase models by intramolecular NH···O hydrogen bonds.

机构信息

Department of Macromolecular Science, Graduate School of Science, Osaka University , Toyonaka, Osaka 560-0043, Japan.

出版信息

J Am Chem Soc. 2014 Oct 22;136(42):14639-41. doi: 10.1021/ja509006x. Epub 2014 Oct 10.

Abstract

Magnesium-dependent phosphatase models containing intramolecular NH···O hydrogen bonds were synthesized and structurally characterized by X-ray analysis. The Mg-O bond distances varied with the mode of the hydrogen bonds. (1)H NMR spectra in nonpolar solvents revealed that the acidity of the coordinated water molecule was regulated by the hydrogen bonds. Further, stoichiometric hydrolysis of phosphoric ester significantly depended on the hydrogen bonds. Zinc analogues showed similar but smaller dependencies, which suggest the indispensable role of Mg(2+) ion in the activation of the enzymes.

摘要

含有分子内 NH···O 氢键的镁依赖性磷酸酶模型通过 X 射线分析进行了合成和结构表征。Mg-O 键距离随氢键的模式而变化。非极性溶剂中的 1H NMR 谱表明,配位水分子的酸性受氢键调节。此外,磷酸酯的化学计量水解明显取决于氢键。锌类似物表现出相似但较小的依赖性,这表明 Mg(2+)离子在酶的激活中起着不可或缺的作用。

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