Abstract
A procedure was developed to isolate fractions enriched in plasma membrane from Caenorhabditis elegans. Coenzyme Q 9 (Q 9) was found in plasma membrane isolated from either wild-type or long-lived qm30 and qm51 clk-1 mutant strains of Caenorhabditis elegans, along with dietary coenzyme Q 8 (Q 8) and the biosynthetic intermediate demethoxy-Q 9 (DMQ 9). NADH was able to reduce both Q 8 and Q 9, but not DMQ 9. Our results indicate that DMQ 9 cannot achieve the same redox role of Q 9 in plasma membrane, suggesting that proportion of all these Q isoforms in plasma membrane must be an important factor in establishing the clk-1 mutant phenotype.
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