Publication year
2014Source
Philosophical Transactions - Royal Society. Biological Sciences, 369, 1646, (2014), pp. 20130446ISSN
Publication type
Article / Letter to editor

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Organization
Biochemistry (UMC)
Paediatrics - OUD tm 2017
CMBI
Journal title
Philosophical Transactions - Royal Society. Biological Sciences
Volume
vol. 369
Issue
iss. 1646
Page start
p. 20130446
Subject
Radboudumc 6: Metabolic Disorders RIMLS: Radboud Institute for Molecular Life SciencesAbstract
Oxygen radical formation in mitochondria is an incompletely understood attribute of eukaryotic cells. Recently, a kinetic model was proposed, in which the ratio between electrons entering the respiratory chain via FADH2 or NADH determines radical formation. During glucose breakdown, the ratio is low; during fatty acid breakdown, the ratio is high (the ratio increasing-asymptotically-with fatty acid length to 0.5, when compared with 0.2 for glucose). Thus, fatty acid oxidation would generate higher levels of radical formation. As a result, breakdown of fatty acids, performed without generation of extra FADH2 in mitochondria, could be beneficial for the cell, especially in the case of long and very long chained ones. This possibly has been a major factor in the evolution of peroxisomes. Increased radical formation, as proposed by the model, can also shed light on the lack of neuronal fatty acid oxidation and tells us about hurdles during early eukaryotic evolution. We specifically focus on extending and discussing the model in light of recent publications and findings.
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- Academic publications [227248]
- Faculty of Medical Sciences [86732]
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