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嗜水气单胞菌的氨那菌素(双(儿茶酚)铁载体)的配位化学(1)。

Coordination Chemistry of the Amonabactins, Bis(catecholate) Siderophores from Aeromonas hydrophila(1).

作者信息

Telford Jason R., Raymond Kenneth N.

机构信息

Department of Chemistry, University of California, Berkeley, California 94720.

出版信息

Inorg Chem. 1998 Sep 7;37(18):4578-4583. doi: 10.1021/ic980090x.

Abstract

The amonabactins are a series of four bis(catecholate) siderophores isolated from the pathogenic organism, Aeromonas hydrophila. As tetradentate ligands, they cannot singly satisfy the octahedral coordination sphere of iron. The solution coordination chemistry of the amonabactins has been elucidated using potentiometric and spectrophotometric titrations, circular dichroism, and mass spectroscopy. They form 2:3 metal:ligand complexes at high pH and excess ligand. Their complexation behavior is essentially identical to one another, with log beta(230) = 86.3. At lower pH, they preferentially form a 1:1 bis(catecholato)bis(aqua) iron(III) species, with log beta(110) = 34.3. The 2:3 complexes show a very slight Delta preference in chirality at the metal center, while the 1:1 complexes are achiral. The biological implications of these properties are discussed.

摘要

氨那巴菌素是从致病生物嗜水气单胞菌中分离出的一系列四种双(儿茶酚)铁载体。作为四齿配体,它们不能单独满足铁的八面体配位球。已使用电位滴定法、分光光度滴定法、圆二色性和质谱法阐明了氨那巴菌素的溶液配位化学。它们在高pH值和过量配体条件下形成2:3的金属:配体配合物。它们的络合行为基本相同,logβ(230) = 86.3。在较低pH值下,它们优先形成1:1的双(儿茶酚)双(水)铁(III)物种,logβ(110) = 34.3。2:3配合物在金属中心的手性上表现出非常轻微的Δ偏好,而1:1配合物是非手性的。讨论了这些性质的生物学意义。

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