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

*Corresponding author for this work
  • University of California, Los Angeles
    ,
  • Dept. of Chemistry and Biochemistry
Research Output:
Contribution to journal
Article
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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.

Bibliographic Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 2395-2398 (4 pages)

Journal (Volume, Issue Number)

Tetrahedron Letters (Volume 37, Issue 14)

Publication milestones

  • Published - 01/04/1996

Publication status

Published - 01/04/1996

ISSN

0040-4039

Publication IDs

  • Scopus: 0029991946