Electronic Structure Analysis of the Dinuclear Metal Center in the Bioremediator Glycerophosphodiesterase (GpdQ) from Enterobacter aerogenes
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- 作者：Kieran S. Hadler ; Nataa Miti ; Sylvia Hsu-Chen Yip ; Lawrence R Gahan ; David L. Ollis ; Gerhard Schenk ; James A. Larrabee
- 刊名：Inorganic Chemistry
- 出版年：2010
- 出版时间：March 15, 2010
- 年：2010
- 卷：49
- 期：6
- 页码：2727-2734
- 全文大小：844K
- 年卷期：v.49,no.6(March 15, 2010)
- ISSN：1520-510X
文摘
The glycerophosphodiesterase (GpdQ) from Enterobacter aerogenes is a promiscuous, dinuclear metallohydrolase that has potential application in the remediation of organophosphate nerve agents and pesticides. GpdQ employs an unusual reaction mechanism in which the enzyme is predominantly mononuclear in the resting state, and substrate binding induces the formation of the catalytically competent dinuclear center (Hadler et al. J. Am. Chem. Soc. 2008, 130, 14129). Reactivity is further modulated by the coordination flexibility of Asn80, a ligand that binds to the second, loosely bound metal ion (Hadler et al. J. Am. Chem. Soc. 2009, 131, 11900). It is proposed that hydrolysis is initiated by a terminal, metal-bound hydroxide molecule which is activated at unusually low pH by electrostatic/hydrogen bonding interactions with a bridging hydroxide species. In this study, electronic structure analysis of the dinuclear center is employed to study the coordination environment of the dinuclear center at the resting and product-bound stage of catalysis. This is achieved through the use of variable temperature, variable field magnetic circular dichroism experiments involving the Co(II)-substituted wild type enzyme and its Asn80Asp variant. The data support the above model for the catalytic mechanism whereby the metal ion-bridging hydroxide molecule activates a terminally bound hydroxide nucleophile. Replacement of Asn80 by an aspartate residue does prevent coordination flexibility but also leads to cleavage of the μ-hydroxide bridge and reduced reactivity. This is the first study to investigate the electronic structure of an enzyme with a μ-1,1-carboxylate bridged dicobalt(II) center.