Assigning the EPR Fine Structure Parameters of the Mn(II) Centers in Bacillus subtilis Oxalate Decarboxylase by Site-Directed Mutagenesis and DFT/MM Calculations
| Autor: | Andrew Ozarowski, Lindsey M. Easthon, Whitney F. Kellett, Alexander Angerhofer, Ursula Rothlisberger, Pablo Campomanes, Nigel G. J. Richards, Karen N. Allen |
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| Rok vydání: | 2014 |
| Předmět: |
Magnetic Resonance Spectroscopy
Carboxy-Lyases Decarboxylation Inorganic chemistry chemistry.chemical_element Manganese Crystallography X-Ray Models Biological Biochemistry Article Catalysis Oxalate law.invention Oxalate decarboxylase chemistry.chemical_compound Colloid and Surface Chemistry law QD Formate Electron paramagnetic resonance Binding Sites General Chemistry Nuclear magnetic resonance spectroscopy Lyase Crystallography chemistry Mutagenesis Site-Directed Quantum Theory Bacillus subtilis |
| Zdroj: | Journal of the American Chemical Society |
| ISSN: | 1520-5126 0002-7863 |
| DOI: | 10.1021/ja408138f |
| Popis: | Oxalate decarboxylase (OxDC) catalyzes the Mn-dependent conversion of the oxalate monoanion into CO2 and formate. EPR-based strategies for investigating the catalytic mechanism of decarboxylation are complicated by the difficulty of assigning the signals associated with the two Mn(II) centers located in the N- and C-terminal cupin domains of the enzyme. We now report a mutational strategy that has established the assignment of EPR fine structure parameters to each of these Mn(II) centers at pH 8.5. These experimental findings are also used to assess the performance of a multistep strategy for calculating the zero-field splitting parameters of protein-bound Mn(II) ions. Despite the known sensitivity of calculated D and E values to the computational approach, we demonstrate that good estimates of these parameters can be obtained using cluster models taken from carefully optimized DFT/MM structures. Overall, our results provide new insights into the strengths and limitations of theoretical methods for understanding electronic properties of protein-bound Mn(II) ions, thereby setting the stage for future EPR studies on the electronic properties of the Mn(II) centers in OxDC and site-specific variants. |
| Databáze: | OpenAIRE |
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