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Papers In Press, published online ahead of print April 1, 2007 J. Lipid Res., doi:10.1194/jlr.M600505-JLR200
Journal of Lipid Research, Vol. 48, 890-903, April 2007 On the singular, dual, and multiple positional specificity of manganese lipoxygenase and its G316A mutant
Division of Biochemical Pharmacology, Department of Pharmaceutical Biosciences, Uppsala University Biomedical Center, SE-751 24 Uppsala, Sweden Published, JLR Papers in Press, January 26, 2007.
1 To whom correspondence should be addressed. e-mail: ernst.oliw{at}farmbio.uu.se
Abstract manganese lipoxygenase (Mn-LO) oxygenates 18:3n-3 and 18:2n-6 to bis-allylic 11S-hydroperoxy fatty acids, which are converted to 13R-hydroperoxy fatty acids. Other unsaturated C16-C22 fatty acids, except 17:3n-3, are poor substrates, possibly because of ineffective enzyme activation (MnII
Supplementary key words nonconjugated peroxyls fatty acid oxygenation hydroperoxide isomerase mass spectrometry metalloenzymes dilinoleoyl-glycerophosphatidylcholine thermostability Abbreviations: CP, chiral phase; GPC, glycerophosphatidylcholine; HETE, hydroxyeicosatetraenoic acid; HHTrE, hydroxyhexadecatrienoic acid; HNTrE, hydroxynonadecatrienoic acid; HPETE, hydroperoxyeicosatetraenoic acid; HPHTrE, hydroperoxyhexadecatrienoic acid; HPNTrE, hydroperoxynonadecatrienoic acid; HPODE, hydroperoxyoctadecadienoic acid; HPOTrE, hydroperoxyoctadecatrienoic acid; KETE, ketoeicosatetraenoic acid; KETrE, ketoeicosatrienoic acid; KHTrE, ketohexadecatrienoic acid; KNTrE, ketononadecatrienoic acid; LOX, lipoxygenase; Mn-LO, manganese lipoxygenase; NP, normal-phase; RP, reverse-phase; sLO, soybean lipoxygenase; TPP, triphenylphosphine; UV, ultraviolet
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