How to deal with oxygen radicals stemming from mitochondrial fatty acid oxidation

D. Speijer*, G. R. Manjeri, R. Szklarczyk

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

34 Citations (Web of Science)

Abstract

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 FADH(2) 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 FADH(2) 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.
Original languageEnglish
Article number20130446
JournalPhilosophical Transactions of the Royal Society B-biological Sciences
Volume369
Issue number1646
DOIs
Publication statusPublished - 5 Jul 2014

Keywords

  • radical formation
  • FADH(2)/NADH ratio
  • complex I
  • supercomplex
  • neurodegenerative disorder
  • peroxisome

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