In this paper, we use our quantitative 31P NMR spin trapping methods, already developed for simple oxygen- and carbon-centered radicals, to understand the radical intermediates generated by enzymatic systems and more specifically lipoxygenases. Our methodology rests on the fact that free radicals react with the nitroxide phosphorus compound, 5-diisopropoxy-phosphoryl-5- methyl-1-pyrroline-N-oxide (DIPPMPO), to form stable radical adducts, which are suitably detected and accurately quantified using 31P NMR in the presence of a phosphorus containing internal standard. This system was thus applied to better understand the mechanism of enzymatic oxidation of linoleic acid by soybean lipoxygenases-1 (LOX). The total amount of radicals trapped by DIPPMPO was detected by 31P NMR at different experimental conditions. In particular the effect of dioxygen concentration on the amount of radicals being trapped was studied. At low dioxygen concentration, a huge increase of radicals trapped was observed with respect to the amount of radicals being trapped at normal dioxygen concentrations. © 2011 Published by Elsevier Ltd.

Zoia, L., Perazzini, R., Crestini, C., Argyropoulos, D. (2011). Understanding the radical mechanism of lipoxygenases using (31)P NMR spin trapping. BIOORGANIC & MEDICINAL CHEMISTRY, 19(9), 3022-3028 [10.1016/j.bmc.2011.02.046].

Understanding the radical mechanism of lipoxygenases using (31)P NMR spin trapping

ZOIA, LUCA;
2011

Abstract

In this paper, we use our quantitative 31P NMR spin trapping methods, already developed for simple oxygen- and carbon-centered radicals, to understand the radical intermediates generated by enzymatic systems and more specifically lipoxygenases. Our methodology rests on the fact that free radicals react with the nitroxide phosphorus compound, 5-diisopropoxy-phosphoryl-5- methyl-1-pyrroline-N-oxide (DIPPMPO), to form stable radical adducts, which are suitably detected and accurately quantified using 31P NMR in the presence of a phosphorus containing internal standard. This system was thus applied to better understand the mechanism of enzymatic oxidation of linoleic acid by soybean lipoxygenases-1 (LOX). The total amount of radicals trapped by DIPPMPO was detected by 31P NMR at different experimental conditions. In particular the effect of dioxygen concentration on the amount of radicals being trapped was studied. At low dioxygen concentration, a huge increase of radicals trapped was observed with respect to the amount of radicals being trapped at normal dioxygen concentrations. © 2011 Published by Elsevier Ltd.
Articolo in rivista - Articolo scientifico
Lipoxygenases; Spin trapping; (31)P NMR; Radicals
English
2011
19
9
3022
3028
none
Zoia, L., Perazzini, R., Crestini, C., Argyropoulos, D. (2011). Understanding the radical mechanism of lipoxygenases using (31)P NMR spin trapping. BIOORGANIC & MEDICINAL CHEMISTRY, 19(9), 3022-3028 [10.1016/j.bmc.2011.02.046].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/24935
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