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The biosynthesis of ubiquinone: Synthesis and enzymatic modification of biosynthetic precursors

  • ,
  • Wayne W. Poona(Author)
    ,
  • David C. Mylesa(Author)
    ,
  • Catherine F. Clarkea(Author)
  • aUniversity of California, Los Angeles
    ,
  • bDept. of Chemistry and Biochemistry
Research Output: Contribution to journal Article Peer-review

Abstract

The synthesis of key intermediates in the eukaryotic biosynthetic pathway of ubiquinone (Q) and the biotransformation of these materials with yeast (S.cerevisiae) mitochondria are described. The synthesis of Q aromatic precursors 2, 3, and 4 (n = 3 in all cases) relies on the palladium (0) catalyzed coupling of farnesyl tributylstannane with suitably functionalized aryl halides. Preliminary experiments show that incubation of synthetic substrate 3 with mitochondria from yeast containing the 3,4-dihydroxy-5-hexaprenylbenzoate methyltransferase gene (COQ3) and S-[methyl-3H]adenosyl-L-methionine yields radiolabeled 4.