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Occurrence of high levels of tetracosahexaenoic acid in the jellyfish Aurelia sp.

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Lipids

Abstract

The FA composition of the pelagic jellyfish Aurelia sp. collected from off-shore Western Australia waters was determined by capillary GC and GC-MS, with confirmation of PUFA structure performed by analysis of 4,4-dimethyloxazoline derivatives. PUFA constituted 47.6% of the total FA, with the essential PUFA eicosapentaenoic acid (FPA), arachidonic acid, and DHA accounting for 34%. Of particular interest, the unusual very long chain PUFA 6,9,12,15,18,21-tetracosahexaenoic acid (THA, 24∶6n−3) was present at 9.3%, and the rarely reported 6,9,12,15,18-tetracosapentaenoic acid (24∶5n−6) also was detected at 0.8%. To our knowledge, this represents the first report of THA as a major PUFA in a pelagic marine organism.

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Abbreviations

AA:

arachidonic acid

DMOX:

4,4-dimethyloxazoline

THA:

tetracosahexaenoic acid

TPA:

tetracosapentaenoic acid

VLC-PUFA:

very long chain PUFA

References

  1. Sargent, J.R., and Whittle, J.J. (1981) Lipids and Hydrocarbons in the Marine Food Web, in Analysis of Marine Ecosystems (Longhurst, A.R., ed.), pp. 453–491, Academic Press, London.

    Google Scholar 

  2. Nichols, P.D., Klumpp, D.W., and Johns, R.B. (1986) A Study of Food Chains in Seagrass Communities. IX. Lipid Components and Utilization by Consumers of a Seagrass Community: An Indication of Carbon Source, Comp. Biochem. Physiol. 83B, 103–113.

    CAS  Google Scholar 

  3. Phleger, C.F., Nichols, P.D., and Virtue, P. (1998) Lipids and Trophodynamics of Antarctic Zooplankton, Comp. Biochem. Physiol. B 120, 311–323.

    Article  Google Scholar 

  4. Nelson, M.M., Phleger, R.P., Mooney, B., and Nichols, P.D. (2000) Lipids of Gelatinous Antarctic Zooplankton: Cnidaria and Ctenophora, Lipids 35, 551–559.

    Article  PubMed  CAS  Google Scholar 

  5. Swadling, K.M., Nichols, P.D., Gibson, J.A.E., and Ritz, D.A. (2000) Role of Lipid in the Life Cycles of Ice-Dependent and Ice-Independent Populations of the Copepod Paralabidocera antarctica, Mar. Ecol. Prog. Series 208, 171–182.

    CAS  Google Scholar 

  6. Phillips, K.L., Jackson, G.D., and Nichols, P.D. (2001) The Diet of the Sub-Antarctic Squid Moroteuthis ingens around Macquarie and Heard Islands: Stomach Content and Fatty Acids as Dietary Tracers, Mar. Ecol. Prog. Series 215, 179–189.

    CAS  Google Scholar 

  7. Bradshaw, C., Hindell, M.A., Best, N.J., Phillips, K.L., Wilson, G., and Nichols, P.D. (2003) You Are What You Eat: Estimating Diet Structure of Southern Elephant Seals (Mirounga leonine) Using Blubber Fatty Acids, Proc. Royal Soc. London B: Biol. Sci. 270, 1283–1292.

    Article  Google Scholar 

  8. Jeffs, A.G., Phleger, C.F., Nelson, M.M., Mooney, B.D., and Nichols, P.D. (2002) Marked Depletion of Polar Lipid and Nonessential Fatty Acids Following Settlement by Post-larvae of the Spiny Lobster Jasus verreauxi, Comp. Biochem. Physiol. 131A, 305–311.

    CAS  Google Scholar 

  9. Jeffs, A.G., Nichols, P.D., and Bruce, M. (2001) Lipid Reserves Used by Pueruli of the Spiny Lobster Jasus edwardsii in Crossing the Continental Shelf of New Zealand, Comp. Biochem. Physiol. A 129, 305–311.

    Article  CAS  Google Scholar 

  10. Phleger, C.F., Nelson, M.M., Mooney, B.D., Nichols, P.D., Ritar, A.R., Smith, G.S., Hart, P.R., and Jeffs, A.G. (2001) Lipids and Nutrition of the Southern Rock Lobster, Jasus edwardsii, from Hatch to Puerulus, Mar. Freshwater Res. 52, 1475–1486.

    Article  CAS  Google Scholar 

  11. Russell, F.S. (1970) Medusae of the British Isles II: Pelagic Scyphozoa, with a Supplement to the First Volume on Hydromedusae, Cambridge University Press, Cambridge.

    Google Scholar 

  12. Mayer, A.G. (1910) Medusae of the World, Vols. 1 and 2, The Hydromedusae, Vol. 3, The Scyphomedusae, Carnegie Institution, Washington, DC.

    Google Scholar 

  13. Bligh, E.G., and Dyer, W.M. (1959) A Rapid Method of Total Lipid Extraction and Purification, Can. J. Biochem. Physiol. 35, 911–917.

    Google Scholar 

  14. Christie, W.W. (1998) Mass Spectrometry of Fatty Acids with Methylene-Interrupted Ene-yne Systems, Chem. Phys. 94, 35–41.

    CAS  Google Scholar 

  15. Mansour, M.P., Volkman, J.K., Holdsworth, D.G., Jackson, A.E., and Blackburn, S.I. (1999) Very-Long-Chain (C28) Highly Unsaturated Fatty Acids in Marine Dinoflagellates, Phytochemistry 50, 541–548.

    Article  CAS  Google Scholar 

  16. Sipos, J.C., and Ackman, R.G. (1968) Jellyfish (Cyanea capillata) Lipids: Fatty Acid Composition, J. Fish. Res. Board Can. 25, 1561–1569.

    CAS  Google Scholar 

  17. Hooper, S.N., and Ackman, R.G. (1972) Presence of trans-6-Hexadecenoic Acid in the White Jellyfish Aurelia aurila Lamarck and in a Caribbean Gorgonian, Lipids 7, 624–626.

    CAS  Google Scholar 

  18. Kariotoglou, D.M., and Mastronicolis, S.K. (2001) Sphingophosphonolipids, Phospholipids, and Fatty Acids from Aegean Jellyfish Aurelia aurita, Lipids 36, 1255–1264.

    Article  PubMed  CAS  Google Scholar 

  19. Phleger, C.F., Nelson, M., Mooney, B.D., and Nichols, P.D. (2000) Lipids of Antarctic Salps and Their Commensal Hyperiid Amphipods, Polar Biol. 23, 329–337.

    Article  Google Scholar 

  20. Linko, R.R., and Karinkanta, H. (1970) Fatty Acids of Long Chain Length in Baltic Herring Lipids, J. Am. Oil Chem. Soc. 47, 42–46.

    CAS  Google Scholar 

  21. Murphy, K.J., Mooney, B.D., Mann, N.J., Nichols, P.D., and Sinclair, A.J. (2002) Lipids, FA, and Sterol Composition of New Zealand Green Lipped Mussel (Perna canaliculus) and Tasmanian Blue Mussel (Mytilis edulis), Lipids 37, 587–595.

    PubMed  CAS  Google Scholar 

  22. Rezanka, T. (1989) Very Long Chain Fatty Acids from the Animal and Plant Kingdoms, Prog. Lipid Res. 28, 147–187.

    Article  PubMed  CAS  Google Scholar 

  23. Kawasaki, K.-I., Nabeshima, Y.I., Ishihara, K., Kaneniwa, M., and Ooizumi, T. (2000) High Level of 6,9,12,15,18,21-Tetracosahexaenoic Acid Found in Lipids of Ophiuroidea Ophiura sarsi Lutken, Fish. Sci. 66, 614–615.

    Article  CAS  Google Scholar 

  24. Takagi, T., Kaneniwa, M., and Itabashi, Y. (1986) Fatty Acids in Crinoidea and Ophiuroidea: Occurrence of all-cis-6,9,12, 15,18,21-Tetracosahexaenoic Acid, Lipids 21, 430–433.

    CAS  Google Scholar 

  25. Ota, T., Chihara, Y., Itabashi, Y., and Takagi, T. (1994) Occurrence of all-cis-6,9,12,15,18,21-Tetracosahexaenoic Acid in Flatfish Lipids, Fish. Sci. 60, 171–175.

    CAS  Google Scholar 

  26. Hooper, S.N., Paradis, M., and Ackman, R.G. (1973) Distribution of trans-6-Hexadecenoic Acid, 7-Methyl-7-hexadecenoic Acid and Common Fatty Acids in Lipids of the Ocean Sunfish Mola mola, Lipids 8, 509–516.

    PubMed  CAS  Google Scholar 

  27. Simopoulos, A.P., Leaf, A., and Salem, N., Jr. (1999) Workshop on the Essentiality of and Recommended Dietary Intake for Omega-6 and Omega-3 Fatty Acids, Food Austr. 51, 332–333.

    Google Scholar 

  28. Marra, J. (2002, November) The State of Dietary Supplements, Nutraceut. World, 32–40.

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Correspondence to Peter D. Nichols.

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Nichols, P.D., Danaher, K.T. & Koslow, J.A. Occurrence of high levels of tetracosahexaenoic acid in the jellyfish Aurelia sp.. Lipids 38, 1207–1210 (2003). https://doi.org/10.1007/s11745-003-1180-z

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  • DOI: https://doi.org/10.1007/s11745-003-1180-z

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