Application Notes:
D,L-2,6-Dimethylheptanoic acid is a simple natural product derived in animal tissues from the metabolism of phytol by the
oxidation of phytanic acid which results in the formation of 2,6-dimethylheptanoic acid along with other compounds.1
Phytanic acid and pristanic acid are initially oxidized in peroxisomes to 4,8-dimethylnonanoyl-CoA, which is converted to
the corresponding acylcarnitine (presumably by peroxisomal carnitine octanoyltransferase), and exported to the
mitochondrion. After transport across the mitochondrial membrane and transfer of the acylgroup to coenzyme A, further
oxidation to 2,6-dimethylheptanoyl-CoA occurs.2 The alkyl chain of cholesterol contains 2,6-dimethylheptane which can be
converted to 2,6-dimethylheptanoic acid during the degradation of cholesterol. (2R)-branched chain fatty acids cannot be
enzymaticaly broken down but must first be converted to the (2S) configuration. A mitochondrial enzyme has been found to
convert (2R,6)-dimethylheptanoyl-CoA to its (2S) stereoisomer.3
References:
1. J. Smoot et al. “Structures and concentrations of surfactants in gut fluid of the marine polychaete Arenicola marina” Marine Ecology Progress Series,
Vol. 258, pp. 161-169, 2003
2. N. Verhoeven et al. “Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts” Journal
of Lipid Research, Vol. 39, pg. 66-74, 1998
3. S. Ferdinandusse et al. “Subcellular localization and physiological role of -methylacyl-CoA racemase” Journal of Lipid Research, Vol. 41, pp. 1890-
1896, 2000