کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1391392 | 983256 | 2011 | 9 صفحه PDF | دانلود رایگان |

SummaryCoenzyme Q (Q), an essential component of eukaryotic cells, is synthesized by several enzymes from the precursor 4-hydroxybenzoic acid. Mutations in six of the Q biosynthesis genes cause diseases that can sometimes be ameliorated by oral Q supplementation. We establish here that Coq6, a predicted flavin-dependent monooxygenase, is involved exclusively in the C5-hydroxylation reaction. In an unusual way, the ferredoxin Yah1 and the ferredoxin reductase Arh1 may be the in vivo source of electrons for Coq6. We also show that hydroxylated analogs of 4-hydroxybenzoic acid, such as vanillic acid or 3,4-dihydroxybenzoic acid, restore Q biosynthesis and respiration in a Saccharomyces cerevisiae coq6 mutant. Our results demonstrate that appropriate analogs of 4-hydroxybenzoic acid can bypass a deficient Q biosynthetic enzyme and might be considered for the treatment of some primary Q deficiencies.
Graphical AbstractFigure optionsDownload high-quality image (316 K)Download as PowerPoint slideHighlights
► Inactivation of Coq6 abrogates the C5-hydroxylation in coenzyme Q biosynthesis
► Vanillic acid restores Q biosynthesis and respiration in coq6 S. cerevisiae mutants
► 4-hydroxybenzoic acid analogs bypass a deficient S. cerevisiae Q biosynthetic step
Journal: - Volume 18, Issue 9, 23 September 2011, Pages 1134–1142