4.6 Article

Evolutionarily conserved Δ25(27)-olefin ergosterol biosynthesis pathway in the alga Chlamydomonas reinhardtii

Journal

JOURNAL OF LIPID RESEARCH
Volume 53, Issue 8, Pages 1636-1645

Publisher

ELSEVIER
DOI: 10.1194/jlr.M027482

Keywords

green algae; sterol evolution; cycloartenol; membranes; sterol C24-methyl transferase; sterol C25-reductase

Funding

  1. National Science Foundation Grant [MCB-0929212]
  2. National Institutes of Health Grant [GM-25661]
  3. Direct For Biological Sciences
  4. Div Of Molecular and Cellular Bioscience [0920212] Funding Source: National Science Foundation

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Ergosterol is the predominant sterol of fungi and green algae. Although the biosynthetic pathway for sterol synthesis in fungi is well established and is known to use C24-methylation-C24 (28)-reduction (Delta(24(28))-olefin pathway) steps, little is known about the sterol pathway in green algae. Previous work has raised the possibility that these algae might use a novel pathway because the green alga Chlamydomonas reinhardtii was shown to possess a mevalonate-independent methylerythritol 4-phosphate not present in fungi. Here, we report that C. reinhardtii synthesizes the protosterol cycloartenol and converts it to ergosterol (C24 beta-methyl) and 7-dehydroporiferasterol (C24 beta-ethyl) through a highly conserved sterol C24- methylation-C25-reduction (Delta(25(27))-olefin) pathway that is distinct from the well-described acetate-mevalonate pathway to fungal lanosterol and its conversion to ergosterol by the Delta(24) ((28))-olefin pathway. We isolated and characterized 23 sterols by a combination of GC-MS and proton nuclear magnetic resonance spectroscopy analysis from a set of mutant, wild-type, and 25-thialanosterol-treated cells. The structure and stereochemistry of the final C24- alkyl sterol side chains possessed different combinations of 24 beta-methyl/ethyl groups and Delta(22(23)) E and Delta(25 (27))-double bond constructions. When incubated with [methyl-H-2(3)] methionine, cells incorporated three (into ergosterol) or five (into 7-dehydroporiferasterol) deuterium atoms into the newly biosynthesized 24 beta-alkyl sterols, consistent only with a Delta(25 (27))-olefin pathway.(jlr) Thus, our findings demonstrate that two separate isoprenoid-24-alkyl sterol pathways evolved in fungi and green algae, both of which converge to yield a common membrane insert ergosterol.-Miller, M. B., B. A. Haubrich, Q. Wang, W. J. Snell, and W. D. Nes. Evolutionarily conserved Delta(25(27))-olefin ergosterol biosynthesis pathway in the alga Chlamydomonas reinhardtii. J. Lipid Res. 2012. 53: 1636-1645.

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