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The reaction mechanism of allene oxide synthase: Interplay of theoretical QM/MM calculations and experimental investigations.
- Source :
-
Archives of biochemistry and biophysics [Arch Biochem Biophys] 2011 Mar 01; Vol. 507 (1), pp. 14-25. Date of Electronic Publication: 2010 Jul 21. - Publication Year :
- 2011
-
Abstract
- A combined theoretical and experimental study highlights the reaction mechanism of allene oxide synthase (AOS) and its possible link to hydroperoxide lyase (HPL) pathway. A previously published study (Lee et al., Nature 455 (2008) 363) has shown that the F137 residue is of central importance in differentiating between the AOS and HPL pathways after initial identical steps. In the experimental part of this study, we show that wild-type AOS from Arabidopsis or rice in fact produces both AOS and HPL products in a ratio of about 80:15, something that was found only in trace amounts before. Theoretical calculations successfully map the whole AOS pathway with 13(S)-hydroperoxy linolenic and linoleic acid as substrates. Subsequent calculations investigated the effects of in silico F137L mutation at the suggested diverging point of the two pathways. The results show that QM/MM calculations can reasonably reproduce three out of four experimentally available cases, and confirm that the pathways are energetically very close to each other, thus making a switch from one path to other plausible under different circumstances.<br /> (Copyright © 2010 Elsevier Inc. All rights reserved.)
- Subjects :
- Aldehyde-Lyases metabolism
Alkadienes metabolism
Arabidopsis chemistry
Arabidopsis genetics
Cytochrome P-450 Enzyme System chemistry
Cytochrome P-450 Enzyme System genetics
Epoxy Compounds metabolism
Intramolecular Oxidoreductases chemistry
Intramolecular Oxidoreductases genetics
Linoleic Acids chemistry
Models, Molecular
Mutation
Oryza chemistry
Oryza genetics
Oxides metabolism
Quantum Theory
Arabidopsis enzymology
Cytochrome P-450 Enzyme System metabolism
Intramolecular Oxidoreductases metabolism
Linoleic Acids metabolism
Oryza enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0384
- Volume :
- 507
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Archives of biochemistry and biophysics
- Publication Type :
- Academic Journal
- Accession number :
- 20654573
- Full Text :
- https://doi.org/10.1016/j.abb.2010.07.016