Literature DB >> 8224157

Intraorganellar localization of CoASH-independent phytanic acid oxidation in human liver peroxisomes.

K Pahan1, I Singh.   

Abstract

In human tissues phytanic acid is alpha-oxidized to pristanic acid in peroxisomes. Studies of the intraorganellar site of alpha-oxidation of [1-14C]phytanic acid to pristanic acid in peroxisomes isolated from human liver demonstrate that phytanoyl-CoA ligase is present in the peroxisomal membrane and that the enzyme system for alpha-oxidation of phytanic acid to pristanic acid is in the peroxisomal matrix. In contrast to the beta-oxidation system for fatty acids, the substrate for alpha-oxidation is free phytanic acid. The studies described in this manuscript report a novel fatty acid oxidation system where the substrate for the enzyme system is free fatty acid; however, phytanoyl-CoA ligase regulates the alpha-oxidation of phytanic acid at the organellar (peroxisomal) level.

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Year:  1993        PMID: 8224157     DOI: 10.1016/0014-5793(93)80395-b

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

1.  Peroxisomal localization of alpha-oxidation in human liver.

Authors:  M Casteels; K Croes; P P Van Veldhoven; G P Mannaerts
Journal:  J Inherit Metab Dis       Date:  1997-09       Impact factor: 4.982

Review 2.  Biochemistry of peroxisomes in health and disease.

Authors:  I Singh
Journal:  Mol Cell Biochem       Date:  1997-02       Impact factor: 3.396

3.  Lipid specificity and location of the sterol carrier protein-2 fatty acid-binding site: a fluorescence displacement and energy transfer study.

Authors:  A Frolov; K Miller; J T Billheimer; T H Cho; F Schroeder
Journal:  Lipids       Date:  1997-11       Impact factor: 1.880

  3 in total

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