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Online oxygen kinetic isotope effects using membrane inlet mass spectrometry can differentiate between oxidases for mechanistic studies and calculation of their contributions to oxygen consumption in whole tissues

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Cheah, Mun Hon
Millar, A. Harvey
Myers, Ruth
Day, David
Roth, Justine
Hillier, Warwick
Badger, Murray

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American Chemical Society

Abstract

The reduction chemistry of molecular oxygen underpins the energy metabolism of multicellular organisms, liberating free energy needed to catalyse a plethora of enzymatic reactions. Measuring the isotope signatures of 16O and 18O during O2 reduction can provide insights into both kinetic and equilibrium isotope effects. However, current methods to measure O2 isotope signatures are time consuming and disruptive. This paper describes the application of membrane inlet mass spectrometry (MIMS) to determining the oxygen isotope discrimination of a range of O2-consuming reactions, providing a rapid and convenient method for determining these values. A survey of oxygenase and oxidase reactions provides new insights into previously uncharacterised amino acid oxidase enzymes. Liquid and gas phase measurements show the ease of assays using this approach for purified enzymes, biological extracts and intact tissues.

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Analytical Chemistry 86. 10 (2014): 5171-5178

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