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A density functional investigation of the extradiol cleavage mechanism in non-heme iron catechol dioxygenases
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UNSPECIFIED (2003) A density functional investigation of the extradiol cleavage mechanism in non-heme iron catechol dioxygenases. JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 8 (4). pp. 409-418. doi:10.1007/s00775-002-0430-7 ISSN 0949-8257.
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Official URL: http://dx.doi.org/10.1007/s00775-002-0430-7
Abstract
The mechanism for extradiol cleavage in non-heme iron catechol dioxygenase was modelled theoretically via density functional theory. Based on the Fe-II-His,His,Glu motif observed in enzymes, an active site model complex, [Fe(acetate)(imidazole)(2)(catecholate)(O-2)](-), was optimized for states with six, four and two unpaired electrons (U6, U4 and U2, respectively). The transfer of the terminal atom of the coordinated dioxygen leading to "ferryl" Fe = O intermediates spontaneously generates an extradiol epoxide. The computed barriers range from 19 kcal mol(-1) on the U6 surface to similar to25 kcal mol(-1) on the U4 surface, with overall reaction energies of + 11.6, 6.3 and 7.1 kcal mol(-1) for U6, U4 and U2, respectively. The calculations for a protonated process reveal the terminal oxygen Of O-2 to be the thermodynamically favoured site but subsequent oxygen transfer to the catechol has a barrier of similar to30-40 kcal mol(-1), depending on the spin state. Instead, protonating the acetate group gives a slightly higher energy species but a subsequent barrier on the U4 surface of only 7 kcal mol(-1) relative to the hydroperoxide complex. The overall exoergicity increases to 13 kcal mol(-1). The favoured proton-assisted pathway does not involve significant radical character and has features reminiscent of a Criegee rearrangement which involves the participation of the aromatic ring pi-orbitals in the formation of the new carbon-oxygen bond. The subsequent collapse of the epoxide, attack by the coordinated hydroxide and final product formation proceeds with an overall exoergicity of similar to75 kcal mol(-1) on the U4 surface.
Item Type: | Journal Article | ||||
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Subjects: | Q Science > QD Chemistry | ||||
Journal or Publication Title: | JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY | ||||
Publisher: | SPRINGER-VERLAG | ||||
ISSN: | 0949-8257 | ||||
Official Date: | April 2003 | ||||
Dates: |
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Volume: | 8 | ||||
Number: | 4 | ||||
Number of Pages: | 10 | ||||
Page Range: | pp. 409-418 | ||||
DOI: | 10.1007/s00775-002-0430-7 | ||||
Publication Status: | Published |
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