Biosynthesis of arachidonic acid in the oleaginous microalga Parietochloris incisa (chlorophyceae): Radiolabeling studies

Chiara Bigogno, Inna Khozin-Goldberg, Daniel Adlerstein, Zvi Cohen

    Research output: Contribution to journalArticlepeer-review

    54 Scopus citations

    Abstract

    The fresh-water green alga Parietochloris incisa is the richest plant source of the PUFA arachidonic acid (20:4n-6, AA). To elucidate the biosynthesis of AA in this alga we labeled cultures of P. incisa with radioactive precursors. Pulse chase labeling with acetate resulted in its incorporation via the de novo biosynthesis pathway of FA. However, labeled acetate was also utilized for the elongation of C16 and C18 PUFA. Labeling with [1-14C]oleic acid has shown that the first steps of the lipid-linked FA desaturations utilize cytoplasmic lipids. PC and diacylglyceryltrimethylhomoserine are the major lipids involved as acyl carriers for the Δ12 and Δ6 desaturations of oleic acid, leading sequentially to linoleic and γ-linolenic acids. The latter is released from its lipid carrier and elongated to 20:3n-6, which is reincorporated primarily into PE and PC and finally desaturated to AA. Galactolipids, mostly monogalctosyldiacylglycerol (MGDG), serve as substrates for the chloroplastic Δ12 desaturase and, apparently, the ω3 desaturation, common to higher plants and many green algae. The predominant sequence desaturates the 18:1/16:0 molecular species of MGDG stepwise to the 18:3n-3/16:3n-3 molecular species similar to the prokaryotic pathway of higher plants and green algae.

    Original languageEnglish
    Pages (from-to)209-216
    Number of pages8
    JournalLipids
    Volume37
    Issue number2
    DOIs
    StatePublished - 1 Jan 2002

    ASJC Scopus subject areas

    • Biochemistry
    • Organic Chemistry
    • Cell Biology

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