RT Journal Article
T1 Introducing Mutations to Modify the C13/C9 Ratio in Linoleic Acid Oxygenations Catalyzed by Rabbit 15‐Lipoxygenase: A QM/MM and MD Study
A1 Suardíaz Delrío, Reynier
A1 Masgrau, Laura
A1 Lluch, José
A1 González‐Lafont, Àngels
AB Lipoxygenases (LOs) are a family of nonheme iron-containing enzymes that catalyze the hydroperoxidation of several polyunsaturated fatty acids with a huge regio- and stereospecificity. Mammalian 15-LO-1 yields almost exclusively oxygenation at the C13 position of the linoleic acid (LA), its preferred substrate. This is very important because metabolites derived from oxidation in distinct positions produce opposite physiological effects. We have combined here quantum mechanics/molecular mechanics calculations with molecular dynamics simulations to show how a suitable mutation of the rabbit 15-LO1 enzyme can produce a significant amount of products derived from oxygenation at the C9 position of LA. In effect, the Leu597Val or Leu597Ala mutants are predicted to lead to a diminution of the oxygenation C13/C9 ratio in LA as huge as five orders of magnitude. This shows that the conserved residue Leu597 actually drives the regiospecific hydroperoxidation of LA catalyzed by 15-LO-1 enzyme
PB Wiley
SN 1439-4235
YR 2014
FD 2014
LK https://hdl.handle.net/20.500.14352/92519
UL https://hdl.handle.net/20.500.14352/92519
LA eng
NO Suardíaz, R., Masgrau, L., Lluch, J.M. and González-Lafont, À. (2014), Introducing Mutations to Modify the C13/C9 Ratio in Linoleic Acid Oxygenations Catalyzed by Rabbit 15-Lipoxygenase: A QM/MM and MD Study. ChemPhysChem, 15: 4049-4054. https://doi.org/10.1002/cphc.201402471
NO Ministerio de Economía y Competitividad (España)
NO Generalitat de Catalunya
NO Alianza 4U
DS Docta Complutense
RD 21 abr 2025