본문 바로가기
KERD
논문KCI 등재

Mixotrophic 배양조건에 따른 Euglena gracilis의 성장과 지질에 미치는 영향

Effect of Growth Conditions on the Biomass and Lipid Production of Euglena gracilis Cells Raised in Mixotrophic Culture

2

조회

0

다운로드

1

인용

0

참고문헌

키워드

주제분류수산학

초록

Microalgae are functional foods because they contain special anti-aging inhibitors and other functional components, such as ecosapentaenoic acid (EPA), docosahexaenoic acid (DHA), and omega-3 polyunsaturated fatty acids. Many of these functional dietary components are absent in animals and terrestrial plants. Thus, microalgae are widely utilized in human functional foods and in the feed provided to farmed fish and terrestrial livestock. Many marine organisms consume microalgae, often because they are in an appropriate portion of the cell size spectrum, but also because of their nutritional content. The nutritional requirements of marine organisms differ from those of terrestrial animals. After hatching, marine animals need small live forage species that have high omega-3 polyunsaturated fatty acid contents, including EPA and DHA. Euglena cells have both plant and animal characteristics; they are motile, elliptical in shape, 15-500 μm in diameter, and have a valuable nutritional content. Mixotrophic cell cultivation provided the best growth rates and nutritional content. Diverse carbon (fructose, lactose, glucose, maltose and sucrose) and nitrogen (tryptone, peptone, yeast extract, urea and sodium glutamate) supported the growth of microalgae with high lipid contents. We found that the best carbon and nitrogen sources for the production of high quality Euglena cells were glucose (10 g L–1) and sodium glutamate (1.0 g L–1), respectively.

Abstract

Microalgae are functional foods because they contain special anti-aging inhibitors and other functional components, such as ecosapentaenoic acid (EPA), docosahexaenoic acid (DHA), and omega-3 polyunsaturated fatty acids. Many of these functional dietary components are absent in animals and terrestrial plants. Thus, microalgae are widely utilized in human functional foods and in the feed provided to farmed fish and terrestrial livestock. Many marine organisms consume microalgae, often because they are in an appropriate portion of the cell size spectrum, but also because of their nutritional content. The nutritional requirements of marine organisms differ from those of terrestrial animals. After hatching, marine animals need small live forage species that have high omega-3 polyunsaturated fatty acid contents, including EPA and DHA. Euglena cells have both plant and animal characteristics; they are motile, elliptical in shape, 15-500 μm in diameter, and have a valuable nutritional content. Mixotrophic cell cultivation provided the best growth rates and nutritional content. Diverse carbon (fructose, lactose, glucose, maltose and sucrose) and nitrogen (tryptone, peptone, yeast extract, urea and sodium glutamate) supported the growth of microalgae with high lipid contents. We found that the best carbon and nitrogen sources for the production of high quality Euglena cells were glucose (10 g L–1) and sodium glutamate (1.0 g L–1), respectively.

참고문헌 (34)

  1. Ackman RG, "Marine phytoplankton fatty acids", J Fish Res Board Can, 25, pp.1603~1620 (1968)
  2. Barsanti LR, "Fatty acid content in wild type and WZSL mutant of Euglena gracilis", J Appl Phycol, 12, pp.515~520 (2000)
  3. Bligh EG, "A rapid method of total lipid extraction and purification", Can J Biochem Physiol, 37, pp.911~917 (1959)
  4. Choi JA, "Impact of beta-1, 3-glucan isolated from Euglena gracilis on corneal epithelial cell migration and on wound healing in a rat alkali burn model", Curr Eye Res, 38, pp.1207~1213 (2013)
  5. Duncan DB, "Multiple range and multiple F test", Biometric, 11, pp.1~42 (1955)
  6. Fan KW, "Physiological studies of subtropical mangrove Thraustochytrids", Botanica Marina, 45, pp.50~57 (2002)
  7. Harwood JL, "Fatty acid metabolism", Ann Rev Plant Physiol Plant Mol Biol, 39, pp.101~138 (1988)
  8. Hayashi M, "Dietary value of rotifers and artemia enriched with Euglena gracilis for red sea bream", Nippon uisan Gakkaishi, 59, pp.1051~1058 (1993)
  9. Hayashi M, "Effects of shifting pH in the stationary phase of growth on the chemical composition of Euglena gracilis", Biosci Biotech Biochem, 58, pp.1964~1967 (1994)
  10. Honda D, "Schizochytrium limacinum sp. nov., a new thraustochytrid from a mangrove area in West Pacific Ocean", Mycol Res, 102, pp.439~448 (1998)
  11. James GW, "The Δ8-Desaturase of Euglenagracilis : An alternate pathway for synthsi of 20-carbon polyunsaturated fatty acids", Archiv Biochem Biophy, 365, pp.307~316 (1999)
  12. James CM, "Growth and ω-3 fatty acid and amino acid composition of microalgae under different temperature regimes", Aquaculture, 77, pp.337~351 (1989)
  13. Jiang Y, "Effect of temperature and temperature shift on docosahexaenoic acid production by the marine microalgae Crypthecodiniumcohnii", JAOCS, 77, pp.613~617 (2000)
  14. 허병기, "당농도 및 염농도가 해양미생물 Thraustochytrium aureum ATCC 34304의 성장 및 지질과 DHA 생성에 미치는 영향 규명", KSBB Journal, 20(4), pp.271~277 (2005), 한국생물공학회
  15. 허병기, "탄소원과 질소원의 무게비가 Thraustochytrium aureum ATCC 34304의 성장 및 지방산 조성 특성에 미치는 영향", KSBB Journal, 20(4), pp.266~270 (2005), 한국생물공학회
  16. Mortensen SH, "Fatty acid and elemental composition of the marine diatom Chaetoceros gracilis Schutt. Effect of silicate deprivation, temperature and light intensity", J Exp Mar Bio Ecol, 122, pp.173~185 (1988)
  17. Navarro L, "Comparison of physiological changes in Euglena gracilis during exposure to heavy metals of heterotrophic and autotrophic cells", Comp Biochem Physiol, 116, pp.265~272 (1997)
  18. Neidelman SL, "Effect of temperature on lipid unsaturation", Biotech Genetic, 5, pp.245~268 (1987)
  19. Oliveira MAS, "Growth and chemical composition of Spirulena maxima and Spirulena platensis biomass at different temperatures", Aquacult, 7, pp.261~275 (1999)
  20. Perez-Garcia O, "Heterotrophic cultures of microalgae: Metabolism and potential products", Water Res, 45, pp.11~36 (2011)
  21. Piorreck M, "Biomass production, total protein, chlorophylls, lipids and fatty acids of freshwater green and blue-green algae under different nitrogen regimes", Phytoch, 23, pp.207~216 (1984)
  22. Regnault A, "Lipid composition of Euglena gracilis in relation to carbon-nitrogen balance", Phytochemistry, 40, pp.725~733 (1995)
  23. Renaud SM, "The gross chemical composition and fatty acid composition of 18 species of tropical Australian microalgae for possible use in mariculture", Aquaculture, 170, pp.147~159 (1999)
  24. Rodríguez-Zavala JS, "Increased synthesis of a-tocopherol, paramylon and tyrosine by Euglena gracilis under conditions of high biomass production", J Appl Microbiol, 1096, pp.2160~2172 (2010)
  25. Ruiz LB, "Isolation, culture and characterization of a new strain of Euglena gracilis. New strain of Euglena gracilis", Phycol Res, 52, pp.168~174 (2004)
  26. Sajbidor J, "Arachidonic acid production by Mortierella sp. S-17: influence of C", N ratio, 1990, pp.12, 455~456
  27. Satu N, "Temperature shift-induced responses in lipids in the blue-green alga, Anabaena variabilis: The central role of diacylmonoalactosyl glycerol in thermoadaption", Biochim Biophys Acta, 619, pp.353~365 (1980)
  28. Thompson PA, "Effects of variation in temperature: ωⅡ. On the fatty acid composition of eight species of marine phytoplankton", J Phycol, 28, pp.488~497 (1992)
  29. Wang H, "Mixotrophic cultivation of Chlorella pyrenoidosa with diluted primary piggery wastewater to produce lipids", Biores Tech, 104, pp.215~220 (2012)
  30. Watanabe K, "Lipid and fatty acid composition of a novel docosahexaenoic acid producing marine bacterium", Lipids, 32, pp.975~978 (1997)
  31. Wen ZY, "Heterotrophic production of eicosapentaenoic acid by microalgae", Biotech Advances, 21, pp.273~294 (2003)
  32. Wu ST, "Effect of culture conditions on docosahexaenoic acid production by Schizochytrium sp. S31", Process Biochem, 40, pp.3103~3108 (2005)
  33. Yokochi T, "Optimization of docosahexaenoic acid production by Schizochytrium limacium SR21", Appl Microbiol Biotechnol, 49, pp.72~76 (1998)
  34. Zhu L, "Changes of lipid content and fatty acid composition of Schizochytrium limacinum in response to different temperatures and salinities", Process Biochem, 42, pp.210~214 (2007)

관련 논문AI추천

이 간행물의 다른 논문 (9건)