DOI QR코드

DOI QR Code

Physiological Properties of Extracts and the Chemical Composition of Tetraselmis sp. JK-46 Cultured with Deep Seawater

해양심층수로 배양한 해양미세조류 Tetraselmis sp. JK-46의 성분 조성 및 생리활성

  • Joo, Dong-Sik (Deprtment of Foodservice Industry, Hanzhong University) ;
  • Kim, Kwang-Woo (Deprtment of Food Science, Kangnung National University) ;
  • Cho, Soon-Yeong (Deprtment of Food Science, Kangnung National University)
  • Received : 2010.10.22
  • Accepted : 2011.02.10
  • Published : 2011.02.28

Abstract

This study examined Tetraselmis sp. JK-46 isolated from seawater from the East Sea. Deep seawater (DSW) had a greater effect on the growth of Tetraselmis sp. JK-46 than surface seawater (SSW). The crude protein, lipid, carbohydrate and ash contents of Tetraselmis sp. JK-46 cultured with DSW were 27.2, 37.1, 13.2 and 26.3 %, respectively, and these values were similar to the results for samples cultured with SSW. The contents of Mg, Ca, Fe and K in the DSW cultured samples were 7080.3, 1009.6, 251.2, and 2749.7 mg/100 g, respectively. The fatty acid compositions of Tetraselmis sp. JK-46 cultured with DSW and SSW were 53.7 and 49.0 % polyunsaturated fatty acids (PUFA) and 25.7 and 30.7 % saturated fatty acids (SFA), respectively. The total amino acid contents of the samples cultured with DSW and SSW were 7392.6 and 6376.0 mg/100 g respectively. The 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity of Tetraselmis sp. JK-46 extracts increased with the concentration of the chloroform and ethyl acetate fractions. The half maximal inhibitiory concentrations ($IC_{50}$) of the chloroform and ethyl acetate fractions of DSW and SSW cultured samples were 1.2 and 2.6 mg/mL, and 3.1 and 3.3 mg/mL, respectively. The ethyl acetate fractions of DSW and SSW cultured samples has anticoagulant activity and the activated partial thromboplastin times (APTT) were 93.4 and 89.3 sec., respectively. The chloroform and ethyl acetate fractions showed antimicrobial activity against Bacillus subtilis, Escherichia coli and Candida albicans.

Keywords

References

  1. AOAC. Offical Methods of Analysis. 16th ed. 1995. Association of Official Analytical Chemists, Washington DC., U.S.A., 69-74.
  2. Borowitzka MA. 1997. Microalgae for aquaculture:opportunities and constraints. J Appl Phycol 9, 393-401. https://doi.org/10.1023/A:1007921728300
  3. Brown MR and Jeffrey SW. 1992. Biochemical composition of microalgae from the green algal classes Chlorophyceae and Prasinophyceae. 1. Amino acids, sugars and pigments. J Exp Mar Biol Ecol 161, 91-113. https://doi.org/10.1016/0022-0981(92)90192-D
  4. Choi JS, Lee WK, Son BW, Kim DS, Choi HD, Choi JS, Jung JH, Im KS and Choi WC. 2000. Screening on radical scavenging activity of marine microalgae. Kor J Pharmacogn 31, 252-255.
  5. Dionisi F, Golay PA, Elli M and Fay LB. 1993. Stability of cyclopropane and conjugated linoleic acids during fatty acid quantification in lactic acid bacteria. Lipids 34, 1107-1115.
  6. Guillard RRL. 1975. Division rates. In: stein J.R.(ed), Handbook of phycological methods-culture methods and growth measurements. Cambridge University Press, Cambridge, U.S.A., 289-311.
  7. Hatano T, Kagawa H and Okawa T. 1988. Two new flavonoids and other constituents in licorice wet: their relative astringency and radical scavening effect. Chem Pharm Bull 36, 2090-2097. https://doi.org/10.1248/cpb.36.2090
  8. John DB. 1982. Clinical Laboratory Methods. Ninth Edition. The C.V. Mosby company. St. Louis, U.S.A., 294-296.
  9. Joo DS and Lee EH. 1998. Searching of antimicrobial active compounds from microalgae. Kor Soc Life Sci 8, 173-180.
  10. Jorian V. 1991. Antibiotics laboratory medicine, Williams & Wilkins, Baltimore. U.S.A., 17-105
  11. Kim SK, Baek HC, Byun HG, Kang OJ and Kim JB. 2001. Biochemical composition and antioxidative activity of marine microalgae. J Kor Fish Soc 34,260-267.
  12. Kim ML, Jeong JS, Lee MH and Lee GD. 2003. Effects of deep seawater and salt on the quality characteristics of breads. Kor J Food Pres 10, 326-332.
  13. Kim SS, Lee CK, Kang SS, Jung HA and Choi JS. 1997. Chlorogenic acid, an antioxidant principle from the aerial parts of Artemisia iwayomogi that acts on DPPH radicak. Arch Pharm Res 20, 148-154. https://doi.org/10.1007/BF02974002
  14. Korea ocean reserch lab. 2000. feasibility study for the multipurpose development of deep ocean water resource. MOMAF Report UCM, 00903-2284.
  15. Laurent D, Patrick G, Yaron A, Shoshana MA, Philippe B, Kotamballi NCM and Gokare AR. 2005. Microorganisms and microalgae as sources of pigments for food use: a scientific oddity or an industrial reality. Trends Food Sci Technol 16, 389-406. https://doi.org/10.1016/j.tifs.2005.02.006
  16. Park EK, Seo MW and Lee CG. 2001. Effect of medium compositions for the growth and the astaxanthin production of Hamatococcus pluviatis. Kor J Appl Microbiol Biotechnol 29, 227-233.
  17. Robles medina A, Molina grima E, Gimenez gimenez and Ibanez gonzalez MJ. 1998. Downstream processing of algal polyunsaturated fatty acids. Biotechnol Adv 16, 517-580. https://doi.org/10.1016/S0734-9750(97)00083-9
  18. Shimma Y, Tanaka H, Huruta Y, Shimma H and Ikeda K. 1984. Protein, carotenoid and mineral contents and fatty acids composition of the sessile algae from Chikuma river. Bull Jap Soc 50, 1223-1227. https://doi.org/10.2331/suisan.50.1223
  19. Takahashi M. 2001. It knows and the deep sea water. Doseo publication, Science and technology 23, 35-37.
  20. Watanabe T, Kitajima C and Jujita S. 1983. Nutrition value of live organisms used in Japan for mass propagation of fish: A review. Aquaculture 34, 115-143. https://doi.org/10.1016/0044-8486(83)90296-X

Cited by

  1. Optimization of Alkail Extraction for Production of Protein Concentrates from Lipid Extracted Algae vol.32, pp.4, 2017, https://doi.org/10.7841/ksbbj.2017.32.4.286
  2. Effects of Scenedesmus deserticola JD052 Extracts on UV-induced Skin Irritation vol.16, pp.1, 2011, https://doi.org/10.20402/ajbc.2017.0169