Marine microalgae Pavlova viridis and Nannochloropsis sp. as n-3 PUFA source in diets for juvenile European sea bass (Dicentrarchus labrax L.)

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• 作者：S. Haas ; J. L. Bauer ; A. Adakli ; S. Meyer ; S. Lippemeier…
• 关键词：Fish feed ; Polyunsaturated fatty acids ; Microalgae ; Pavlova ; Nannochloropsis
• 刊名：Journal of Applied Phycology
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：28
• 期：2
• 页码：1011-1021
• 全文大小：552 KB
• 参考文献：Atalah E, Cruz CMH, Izquierdo MS, Rosenlund G, Caballero MJ, Valencia A, Robaina L (2007) Two microalgae Crypthecodinium cohnii and Phaeodactylum tricornutum as alternative source of essential fatty acids in starter feeds for seabream (Sparus aurata). Aquaculture 270:178–185CrossRef
  Becker W (2004) Microalgae in human and animal nutrition. In: Richmond A (ed) Handbook of microalgal culture. Blackwell, Oxford, pp 312–351
  Bell JG, Sargent JR (2003) Arachidonic acid in aquaculture feeds: current status and future opportunities. Aquaculture 218:491–499CrossRef
  Bell JG, McEvoy J, Tocher DR, McGhee F, Campbell PJ, Sargent JR (2001) Replacement of fish oil with rapeseed oil in diets of Atlantic salmon (Salmo salar) affects tissue lipid compositions and hepatocyte fatty acid metabolism. J Nutr 131:1535–1543PubMed
  Bendif EM, Probert I, Hervé A, Billard C, Goux D, Lelong C, Cadoret J-P, Véron B (2011) Integrative taxonomy of the Pavlovophyceae (Haptophyta): a reassessment. Protist 162:783–761CrossRef
  Borowitzka MA (1997) Microalgae for aquaculture: opportunities and constraints. J Appl Phycol 9:393–401CrossRef
  Brown MR, Mular M, Miller I, Farmer C, Trenerry C (1999) The vitamin content of microalgae used in aquaculture. J Appl Phycol 11:247–255CrossRef
  Bruce M, Oyen F, Bell G, Asturiano JF, Farndale B, Carrillo M, Zanuy S, Ramos J, Bromage N (1999) Development of broodstock diets for the European Sea Bass (Dicentrarchus labrax) with special emphasis on the importance of n − 3 and n − 6 highly unsaturated fatty acid to reproductive performance. Aquaculture 177:85–97CrossRef
  Bureau DP, Kaushik SJ, Cho CY (2002) Bioenergetics. In: Halver JE, Hardy RW (eds) Fish nutrition. Elsevier Science, USA, pp 2–61
  Castell JD, Bell JG, Tocher DR, Sargent JR (1994) Effects of purified diets containing different combinations of arachidonic and docosahexaenoic acid on survival, growth and fatty acid composition of juvenile turbot (Scophthalmus maximus). Aquaculture 128:315–333CrossRef
  Corraze G, Kaushik S (1999) Les lipides des poissons marins et d’eau douce. Oléagineux Corps Gras Lipids 6:111–115
  EU guideline (EC) 152/2009 Commission regulation laying down the methods of sampling and analysis for the official control of feed. 130 pp
  Figueiredo-Silva A, Rocha E, Dias J, Silva P, Rema P, Gomes E, Valente LMP (2005) Partial replacement of fish oil by soybean oil on lipid distribution and liver histology in European sea bass (Dicentrarchus labrax) and rainbow trout (Oncorhynchus mykiss) juveniles. Aquac Nutr 11:147–155CrossRef
  Folch J, Lees M, Sloane-Stanley GH (1957) A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 226:497–509PubMed
  Glencross BD (2009) Exploring the nutritional demand for essential fatty acids by aquaculture species. Rev Aquac 1:71–124CrossRef
  Izquierdo MS, Obach A, Arantzamendi L, Montero D, Robaina L, Rosenlund G (2003) Dietary lipid sources for seabream and seabass: growth performance, tissue composition and flesh quality. Aquac Nutr 9:397–407CrossRef
  Llames C, Fontaine J (1994) Determination of amino acids in feeds: collaborative study. J AOAC Int 77:1362–1402
  Miller MR, Nichols PD, Carter CG (2007) Replacement of fish oil with thraustochytrid Schizochytrium sp. L oil in Atlantic salmon parr (Salmo salar L) diets. Comp Biochem Phys A 148:382–392CrossRef
  Navarro N, Sarasquete C (1998) Use of freeze-dried microalgae for rearing gilthead seabream, Sparus aurata, larvae: I. Growth, histology and water quality. Aquaculture 167:179–193CrossRef
  Naylor RL, Hardy RW, Bureau DP, Chiu A, Elliott M, Farrell AP, Forster I, Gatlin DM III, Goldburg RJ, Hua K (2009) Feeding aquaculture in an era of finite resources. Proc Natl Acad Sci 106:15103–15110CrossRef PubMed PubMedCentral
  Norsker NH, Barbosa MJ, Vermuë MH, Wijffels RH (2011) Microalgal production—a close look at the economics. Biotechnol Adv 29:24–27CrossRef PubMed
  Olvera‐Novoa MA, Dominguez‐Cen LJ, Olivera‐Castillo L, Martínez‐Palacios CA (1998) Effect of the use of the microalga Spirulina maxima as fish meal replacement in diets for tilapia, Oreochromis mossambicus (Peters), fry. Aquac Res 29:709–715CrossRef
  Patil V, Källqvist T, Olsen E, Vogt G, Gislerød H (2007) Fatty acid composition of 12 microalgae for possible use in aquaculture feed. Aquac Int 15:1–9CrossRef
  Pereira S, Leonard A, Huang Y, Chuang L, Mukerji P (2004) Identification of two novel microalgal enzymes involved in the conversion of the omega3-fatty acid, eicosapentaenoic acid, into docosahexaenoic acid. Biochem J 384:357–366CrossRef PubMed PubMedCentral
  Qiao H, Wang H, Song Z, Ma J, Li B, Liu X, Zhang S, Wang J, Zhang L (2014) Effects of dietary fish oil replacement by microalgae raw materials on growth performance, body composition and fatty acid profile of juvenile olive flounder, Paralichthys olivaceus. Aquac Nutr 20:646–653CrossRef
  RAFOA (2005) Researching Alternatives to Fish Oils in Aquaculture. http://​www.​rafoa.​stir.​ac.​uk/​project_​results.​html . Accessed January 29 2015
  Regost C, Arzel J, Robin J, Rosenlund G, Kaushik SJ (2003) Total replacement of fish oil by soybean or linseed oil with a return to fish oil in turbot (Psetta maxima): 1. Growth performance, flesh fatty acid profile, and lipid metabolism. Aquaculture 217:465–482CrossRef
  Roy SS, Pal R (2015) Microalgae in aquaculture: a review with special references to nutritional value and fish dietetics. Proc Zool Soc 68:1–8CrossRef
  Ruyter B, Rosjo C, Einen O, Thomassen MS (2000) Essential fatty acids in Atlantic salmon: time course of changes in fatty acid composition of liver, blood and carcass induced by a diet deficient in n-3 and n-6 fatty acids. Aquac Nutr 6:109–118CrossRef
  Sargent JR, Tocher DR, Bell JG (2002) The lipids. Fish Nutr 3:181–257
  Simopoulos AP (1991) Omega-3 fatty acids in health and disease and in growth and development. Am J Clin Nutr 54:438–463PubMed
  Skalli A, Robin JH (2004) Requirement of n-3 long chain polyunsaturated fatty acids for European sea bass (Dicentrarchus labrax) juveniles: growth and fatty acid composition. Aquaculture 240:399–415CrossRef
  Skrede A, Mydland LT, Ahlstrøm Ø, Reitan KI, Gislerød HR, Øverland M (2011) Evaluation of microalgae as sources of digestible nutrients for monogastric animals. J Anim Feed Sci 20:131–142
  Spolaore P, Joannis-Cassan C, Duran E, Isambert A (2006) Commercial applications of microalgae. J Biosci Bioeng 101:87–96CrossRef PubMed
  Tartiel MB, Ibrahim EM, Zeinhom MM (2008) Partial replacement of fish meal with dried microalgae (Chlorella spp. and Scenedesmus spp.) in Nile Tilapia (Oreochromis niloticus) diets, 8th International Symposium on Tilapia in Aquaculture, pp. 801-811
  Tibaldi E, Kaushik SJ (2005) Amino-acid requirements of Mediterranean fish species. Cah Opt Med 63:59–65
  Tibaldi E, ChiniZittelli G, Parisi G, Bruno M, Giorgi G, Tulli F, Venturini S, Tredici MR, Poli BM (2015) Growth performance and quality traits of European sea bass (D. labrax) fed diets including increasing levels of freeze-dried Isochrysis sp. (T-ISO) biomass as a source of protein and n-3 long chain PUFA in partial substitution of fish derivatives. Aquaculture 440:60–68CrossRef
  Tulli F, Chini Zittelli G, Giorgi G, Poli BM, Tibaldi E, Tredici MR (2012) Effect of the inclusion of dried Tetraselmis suecica on growth, feed utilization and fillet composition of European sea bass juveniles fed organic diets. J Aquat Food Prod Technol 21:1–11CrossRef
  Vizcaíno A, López G, Sáez M, Jiménez J, Barros A, Hidalgo L, Camacho-Rodríguez J, Martínez T, Cerón-García M, Alarcón F (2014) Effects of the microalga Scenedesmus almeriensis as fishmeal alternative in diets for gilthead sea bream, Sparus aurata, juveniles. Aquaculture 431:34–43CrossRef
  Volkman JK, Jeffrey SW, Nichols PD, Rogers GI, Garland CD (1989) Fatty acid and lipid composition of 10 species of microalgae used in mariculture. J Exp Mar Biol Ecol 128:219–240CrossRef
  Volkman JK, Dunstan GA, Jeffrey SW, Kearney PS (1991) Fatty acids from microalgae of the genus Pavlova. Phytochemistry 30:1855–1859CrossRef
  Waldenstedt L, Inborr J, Hansson I, Elwinger K (2003) Effects of astaxanthin-rich algal meal (Haematococcus pluvalis) on growth performance, caecal campylobacter and clostridial counts and tissue astaxanthin concentration of broiler chickens. Anim Feed Sci Technol 108:119–132CrossRef
  Watanabe T (1982) Lipid nutrition in fish. Comp Biochem Physiol B 73:3–15
  Yone Y, Fujii M (1975) Studies on nutrition of red sea bream, 12: effect of omega-3 fatty acid supplement in a corn oil diet on fatty acid composition of fish. Bull Jap Soc Sci Fish 41:79–86 
  Zeinhom MM (2004) Nutritional and physiological studies on fish, Faculty of Agriculture. Zagazig University, Egypt, 102 pp
  
• 作者单位：S. Haas (1) (5)
  J. L. Bauer (2)
  A. Adakli (3)
  S. Meyer (1)
  S. Lippemeier (4)
  K. Schwarz (2)
  C. Schulz (1) (5)
  
  1. GMA – Gesellschaft für Marine Aquakultur mbH, Büsum, Germany
  5. Institute of Animal Breeding and Husbandry, Christian-Albrechts-University, Kiel, Germany
  2. Department of Food Technology, Institute of Human Nutrition and Food Science, Christian-Albrechts-University, Kiel, Germany
  3. Fisheries Faculty, Department Aquaculture, Cukurova University, Adana, Turkey
  4. BlueBioTech GmbH, Büsum, Germany
  
• 刊物主题：Plant Sciences; Freshwater & Marine Ecology; Plant Physiology; Ecology;
• 出版者：Springer Netherlands
• ISSN：1573-5176

文摘

In the present study, the potential of the microalga Pavlova viridis (=Diacronema viridis) as an n-3 polyunsaturated fatty acid (PUFA) source was evaluated and compared to Nannochloropsis sp. in diets for juvenile European sea bass (Dicentrarchus labrax L.) (initial weight ~12.8 ± 1.7 g) in an 8-week feeding trial. Six different isoenergetic and isonitrogenous test diets were used: (1) fish oil diet (FO), major lipid source fish oil (100 %), (2) basal diet, 40 % fish oil and 60 % plant oil (in equal parts rapeseed, sunflower, and linseed oil), (3) Pavlova 50 % (P50), 50 % of the fish oil of the basal diet was substituted by lipid content of P. viridis meal, (4) Pavlova 100 % (P100), 100 % of the fish oil of the basal diet was substituted by lipid content of P. viridis meal, (5) Nannochloropsis 50 % (N50), 50 % of the fish oil of the basal diet was substituted by lipid content of Nannochloropsis sp. meal, and (6) Nannochloropsis 100 % (N100), 100 % of the fish oil of the basal diet was substituted by lipid content of Nannochloropsis sp. meal. The specific growth rate was highest and feed conversion ratio was lowest in the P100 group (SGR 1.77 ± 0.10 % day−1; FCR 1.17 ± 0.01), although not significantly different to the results for the FO and the other algae-groups. Furthermore, the sum of PUFA was also highest in the P100 group, followed by the P50, N100, N50, and B group (mainly due to the high content of linoleic and linolenic acids coming from plant oils and microalgal products) with the lowest levels in the FO group. The highest amounts of docosahexaenoic acid (DHA) of total fatty acids were found in the FO and B group, although not significantly higher than in groups P50 and P100. The significantly highest amount of eicosapentaenoic acid (EPA, % of total fatty acids) was in the P100 samples and the lowest amount was in samples of the basal group. The histological analyses of liver and intestine samples did not reveal any negative effects caused by the experimental treatments. Based on the basal diet, a 50 % fish oil replacement by Nannochloropsis sp. meal and a total replacement by P. viridis meal were possible without negative effects on the growth performance and nutrient utilization of juvenile sea bass.