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The lipid composition of the abdominal muscle of shrimp Crangon crangon from the Gulf of Gdansk in spring and winter periods

Published online by Cambridge University Press:  04 June 2013

Adriana Mika
Affiliation:
Institute for Environmental and Human Health Protection, University of Gdansk, ul. Sobieskiego 18/19, 80-952 Gdansk, Poland Faculty of Biology, University of Gdansk, Wita Stwosza 59, 80-308 Gdansk, Poland
Edward Skorkowski
Affiliation:
Faculty of Biology, University of Gdansk, Wita Stwosza 59, 80-308 Gdansk, Poland
Piotr Stepnowski
Affiliation:
Institute for Environmental and Human Health Protection, University of Gdansk, ul. Sobieskiego 18/19, 80-952 Gdansk, Poland
Marek Gołębiowski*
Affiliation:
Institute for Environmental and Human Health Protection, University of Gdansk, ul. Sobieskiego 18/19, 80-952 Gdansk, Poland
*
Correspondence should be addressed to: M. Gołębiowski, Institute for Environmental and Human Health Protection University of Gdansk, ul. Sobieskiego 18/19, 80-952 Gdansk, Poland email: goleb@chem.univ.gda.pl

Abstract

The composition of fatty acids and sterols of Crangon crangon abdomen muscle was determined during two periods in the year 2010/2011. For determination of lipids classes, especially of fatty acids and sterols, high performance liquid chromatography with a laser light-scattering detector and gas chromatography–mass spectrometry were applied. Diversity and variety of saturated and unsaturated fatty acids was the highest during the spring period. Twenty-seven free fatty acids with from nine to 24 carbon atoms were determined in the spring periods. Among this fraction, 14 saturated and 13 unsaturated fatty acids (eight mono- and five polyunsaturated) were present. Only seven saturated and four unsaturated free fatty acids (14:2, 17:1, 16:1 and 18:1) were identified in December 2010. Arachidonic acid (20:4) and eicosapentaenoic acid (20:5) were detected in these two periods, and during the spring season an additional essential fatty acid—docosahexaenoic acid (22:6)—was present, which was not detected in the winter period. The number of identified sterols was correlated with phytoplankton, which was abundant during April 2011. Also, the sterol fraction in winter periods was very poor—only cholesterol was detected.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2013 

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References

REFERENCES

Abad, M., Ruiz, C., Martinez, D., Mosquera, G. and Sánchez, J.L. (1995) Seasonal variations of lipids classes and fatty acids in flat oyster Ostrea edulis, from San Cibran (Galicia, Spain). Comparative Biochemistry and Physiology 110C, 109118.Google Scholar
Alexander, J.W. (1998) Immunonutrition: the role of ω-3 fatty acids. Nutrition 14, 627633.Google Scholar
Allen, C.E. (1999) Lipid profiles of deep-sea organisms. PhD thesis. University of Southampton, UKGoogle Scholar
Amara, R., Laffargue, P., Dewarumez, J.M., Maryniak, C., Lagardère, F. and Luczac, C. (2001) Feeding ecology and growth of 0-group flatfish (sole, dab and plaice) on a nursery ground (southern Bight of the North Sea). Journal of Fish Biology 25, 788803.Google Scholar
Boutry, J.L., Saliot, A. and Barbier, M. (1979) The diversity of marine sterols and the role of algal bio-masses; from facts to hypothesis. Experientia 35, 15411684.CrossRefGoogle ScholarPubMed
Bragagnolo, N. and Rodriguez-Amaya, D.B. (2001) Total lipid, cholesterol, and fatty acids of farmed freshwater prawn (Macrobrachium rosenbergii) and wild marine shrimp (Penaeus brasiliensis, Penaeus schimitti, Xiphopenaeus kroyeri). Journal of Food Composition and Analysis 14, 359369.CrossRefGoogle Scholar
Campos, J., Van der Veer, H.W., Freitas, V. and Kooijman, S.A.L.M. (2009) Contribution of different generations of the brown shrimp C. crangon (L.) in the Dutch Wadden Sea to commercial fisheries: a dynamic energy budget approach. Journal of Sea Research 62, 106113.CrossRefGoogle Scholar
Çelik, M., Türeli, C., Çelik, M., Yanar, Y., Erdem, Ü. and KüÇükgülmez, A. (2004) Fatty acid composition of the blue crab (Callinectes sapidus Rathbun, 1896) in the north eastern Mediterranean. Food Chemistry 88, 271273.CrossRefGoogle Scholar
Clarke, A. (1979) Lipid content and composition of the pink shrimp, Pandalus montagui (Leach) (Crustacea: Decapoda). Journal of Experimental Marine Biology and Ecology 38, 117.CrossRefGoogle Scholar
Coutteau, P. and Mourente, G. (1997) Lipid classes and their content of n-3 highly unsaturated fatty acids (HUFA) in Artemia franciscana after hatching, HUFA-enrichment and subsequent starvation. Marine Biology 130, 8191.CrossRefGoogle Scholar
Donaldson, H.A. (1976) Chemical composition of sergestid shrimps (Decapoda: Natantia) collected near Bermuda. Marine Biology 38, 5158.CrossRefGoogle Scholar
Garofalaki, T.F., Miniadis-Meimaroglou, S. and Sinanoglou, V.J. (2006) Main phospholipids and their fatty acid composition in muscle and cephalothorax of the edible Mediterranean crustacean Palinurus vulgaris (spiny lobster). Chemistry and Physics of Lipids 140, 5565.CrossRefGoogle ScholarPubMed
Gołębiowski, M. (2012) Comparison of free fatty acids composition of cuticular lipids of Calliphora vicina larvae and pupae. Lipids 47, 10011009.CrossRefGoogle ScholarPubMed
Gołębiowski, M., Boguś, M.I., Paszkiewicz, M., Wieloch, W., Włóka, E. and Stepnowski, P. (2012) The composition of the cuticular and internal free fatty acids and alcohols from Lucilia sericata males and females. Lipids 47, 613622.CrossRefGoogle ScholarPubMed
Gołębiowski, M., Cerkowniak, M., Boguś, M.I., Włóka, E., Dawgul, M., Kamysz, W. and Stepnowski, P. (2013) Free fatty acids in the cuticular and internal lipids of Calliphora vomitoria and their antimicrobial activity. Journal of Insect Physiology 59, 416429.CrossRefGoogle ScholarPubMed
Green, K.N., Martinez-Coria, H., Khashwji, H., Hall, E.B., Yurko-Mauro, K.A., Ellis, L. and LaFerla, H.M. (2007) Dietary docosahexaenoic acid and docosapentaenoic acid ameliorate amyloid- and pathology via a mechanism involving presenilin 1 levels. Journal of Neuroscience 27, 43854395.CrossRefGoogle Scholar
Heu, M.-S., Kim, J.-S. and Shahidi, F. (2003) Components and nutritional quality of shrimp processing by-products. Food Chemistry 82, 235242.CrossRefGoogle Scholar
Holthuis, L.B. (1980) Shrimps and prawns of the World—Volume 1. An Annotated Catalogue of Species of Interest to Fisheries. FAO Fisheries Synopsis 125.Google Scholar
Holub, B.J. (2002) Clinical nutrition: 4. ω-3 fatty acids in cardiovascular care. Canadian Medical Association Journal 166, 608615.Google ScholarPubMed
Jeffs, A.G., Phleger, C.F., Nelson, M.M., Mooney, B.D. and Nichols, P.D. (2002) Marked depletion of polar lipid and non-essential fatty acids following settlement by post-larvae of the spiny lobster Jasus erreauxi. Comparative Biochemistry and Physiology 131A, 305311.CrossRefGoogle Scholar
Jung, K. and Zauke, G.P. (2008) Bioaccumulation of trace metals in the brown shrimp C. crangon (Linnaeus, 1758) from the German Wadden Sea. Aquatic Toxicology 88, 243249.CrossRefGoogle ScholarPubMed
Kanazawa, A. (2001) Sterols in marine invertebrates. Fish Science 67, 9971007.CrossRefGoogle Scholar
Kasai, T. and Sakai, H. (2004) Seasonal changes in icosapentaenoic acid and docosahexaenoic acid contents in muscle lipids of Hokkai prawn Pandalus kessleri. Fish Science 70, 527529.CrossRefGoogle Scholar
Le Nechet, S., Dubois, N., Gouygou, J.-P. and Berge, J.-P. (2007) Lipid composition of the liver oil of the ray, Himantura bleekeri. Food Chemistry 104, 559564.CrossRefGoogle Scholar
Lee, R.F., Hagen, W. and Kattner, G. (2006) Lipid storage in marine zooplankton. Marine Ecology Progress Series 307, 273306.CrossRefGoogle Scholar
Limbourn, A.J. and Nichols, P.D. (2009) Lipid, fatty acid and protein content of late larval to early juvenile stages of the western rock lobster, Panulirus cygnus. Comparative Biochemistry and Physiology 152B, 292298.CrossRefGoogle Scholar
Logan, A.L. (2004) ω-3 fatty acids and major depression: a primer for the mental health professional. Lipids Health Disease 3, 18.CrossRefGoogle ScholarPubMed
Luttikhuizen, P.C., Campos, J., van Bleijswijk, J., Peijnenburg, K. and van der Veer, H.W. (2008) Phylogeography of the common shrimp, C. crangon (L.) across its distribution range. Molecular Phylogenetics and Evolution 46, 10151030.CrossRefGoogle ScholarPubMed
Maazouzi, C., Masson, G., Soledad Izquierdo, M. and Pihan, J.-C. (2007) Fatty acid composition of the amphipod Dikerogammarus villosus: feeding strategies and trophic links. Comparative Biochemistry and Physiology 147A, 868875.CrossRefGoogle Scholar
Mika, A., Gołębiowski, M., Szafranek, J., Rokicki, J. and Stepnowski, P. (2010) Identification of lipids in the cuticle of the parasitic nematode Anisakis simplex and the somatic tissues of the Atlantic cod Gadus morhua. Experimental Parasitology 124, 334340.CrossRefGoogle ScholarPubMed
Mika, A., Gołębiowski, M., Skorkowski, E. and Stepnowski, P. (2012) Composition of fatty acids and sterols composition in brown shrimp C. crangon and herring Clupea harengus membras from the Baltic Sea. Oceanological and Hydrobiological Studies 41, 5764.CrossRefGoogle Scholar
Mika, A., Shorkowski, E., Stepnowski, P. and Gołębiowski, M. (2013) Identification of lipid components in the abdominal muscle of fall-caught Crangon crangon from a coastal area of the Baltic Sea. Journal of the Brazilian Chemical Society 24, 439448.Google Scholar
Mourente, G. and Rodriquez, A. (1991) Variation in lipid content of wild caught females of the marine shrimp, Penaeus kerathurus during sexual maturation. Marine Biology 110, 2128.CrossRefGoogle Scholar
Perez-Velazquez, M., Gonzalez-Felix, M.L., Lawrence, A.L. and Gatlin III, D.M. (2003) Changes in lipid class and fatty acid composition of adult male Litopenaeus vannamei (Boone) in response to culture temperature and food deprivation. Aquaculture Research 34, 12051213.CrossRefGoogle Scholar
Philips, B.F., Jeffs, A.G., Melville-Smith, R., Chubb, C.F., Nelson, M.M. and Nichols, P.D. (2006) Changes in lipid and fatty acid composition of late larval and puerulus stages of the spiny lobster (Panulirus cygnus) across the continental shelf of Western Australia. Comparative Biochemistry and Physiology 143B, 219228.CrossRefGoogle Scholar
Selleslagh, J. and Amara, R. (2008) Environmental factors structuring fish composition and assemblages in a small macrotidal estuary (eastern English Channel). European Journal of Lipid Science and Technology 79, 507517.Google Scholar
Sijben, J.W.C. and Calder, P.C. (2007) Differential immunomodulation with long-chain n-3 PUFA in health and chronic disease. Proceedings of the Nutrition Society 66, 237259.CrossRefGoogle ScholarPubMed
Stulnig, T.M. (2003) Immunomodulation by polyunsaturated fatty acids: mechanisms and effects. International Archives of Allergy and Immunology 132, 310321.CrossRefGoogle ScholarPubMed
Tiews, K. (1970) Synopsis of biological data on the common shrimp Crangon crangon (Linnaeus, 1758). FAO Fisheries Report 57, 1167–1224.Google Scholar
Tocher, D.R. (2003) Metabolism and functions of lipids and fatty acids in teleost fish. Reviews in Fisheries Science 11, 107184.CrossRefGoogle Scholar
Van der Veer, H.W. and Bergman, M.J.M. (1987) Predation by crustaceans on a newly settled 0-group of plaice Pleuronectes platessa populations in the Western Wadden Sea. Marine Ecology Progress Series 35, 203215.CrossRefGoogle Scholar
Virtue, P., Nicol, S. and Nichols, P.D. (1993) Changes in the digestive gland of Euphausia superba during short-term starvation: lipid class, fatty acid and sterol content and composition. Marine Biology 117, 441448.CrossRefGoogle Scholar
Yang, L., Zhang, A. and Zheng, X. (2009) Shrimp shell catalyst for biodiesel. Production Energy Fuels 23, 38593865.CrossRefGoogle Scholar
Zhao, S., Jia, L., Gao, P., Li, Q., Lu, X., Li, J. and Xu, G. (2008) Study on the effect of eicosapentaenoic acid on phospholipids composition in membrane microdomains of tight junctions of epithelial cells by liquid chromatography/electrospray mass spectrometry. Journal of Pharmaceutical and Biomedical Analysis 47, 343350.CrossRefGoogle Scholar