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Alpha-oxidation of 3-methyl-substituted fatty acids and its thiamine dependence
Minne Casteels1, Veerle Foulon, Guy P Mannaerts
1Afdeling Farmacologie, Department of Molecular Cell Biology, Katholieke Universiteit Leuven, Belgium. minne.casteels@med.kuleuven.ac.be
European Journal of Biochemistry
|April 16, 2003
Abstract:
3-Methyl-branched fatty acids, as phytanic acid, undergo peroxisomal alpha-oxidation in which they are shortened by 1 carbon atom. This process includes four steps: activation, 2-hydroxylation, thiamine pyrophosphate dependent cleavage and aldehyde dehydrogenation. The thiamine pyrophosphate dependence of the third step is unique in peroxisomal mammalian enzymology. Human pathology due to a deficient alpha-oxidation is mostly linked to mutations in the gene coding for the second enzyme of the sequence, phytanoyl-CoA hydroxylase.