DOI QR코드

DOI QR Code

Purification and Characterization of Complement-activating Acidic Polysaccharides from the Fruits of Capsicum annuum

  • Paik, Soon-Young (Department of Microbiology, College of Medicine, The Catholic University of Korea) ;
  • Ra, Kyung-Soo (Department of Food and Nutrition, Daegu Technical College) ;
  • Chang, In-Seop (Water Environment Research Center, Korea Institute of Science and Technology) ;
  • Park, Yoon-Chang (Division of Life Resources, College of Natural Resources, Daegu University) ;
  • Park, Hee-Sung (Department of Plant Genetic Engineering, Catholic University of Daegu) ;
  • Baik, Hyung-Suk (Department of Microbiology, Pusan National University) ;
  • Yun, Jong-Won (Department of Biotechnology, College of Engineering, Daegu University) ;
  • Choi, Jang-Won (Division of Life Resources, College of Natural Resources, Daegu University)
  • Published : 2003.03.31

Abstract

Hot water-soluble crude polysaccharide (HCAP-0) that was obtained from the fruits of Capsicum annuum showed potent anti-complementary activity. The activity was unchanged by pronase digestion, but decreased by periodate oxidation. The HCAP-0 was fractionated by DEAE ion-exchange chromatography to give two major fractions, HCAP-II and III. These two fractions were finally purified by gel filtration to give HCAP-IIa, HCAP-IIIa1, and IIIa2 fractions that had high anti-complementary activities. The HCAP-IIIa1 and IIIa2 consisted of homogeneous polysaccharides. The anti-complementary activities were unaffected by treatment with polymyxin B, indicating that the modes of complement activation were not due to preexisting lipopolysaccharide. The molecular weight and sugar content of HCAP-IIIa2 had potent anti-complementary activity. The highest yields were 55 kDa and 75.9%, and the molar ratio of galactose (Ara:Gal, 1.0:4.6) was higher than other sugars. The crossed immuno-electrophoresis showed that both classical and alternative pathways were activated by HCAP-IIIa2.

Keywords

References

  1. Blumenkrantz, N. & Asboe-Hansen, G. (1973) New method for quantitative determination of uronic acids. Anal. Biochem. 54. 484-489. https://doi.org/10.1016/0003-2697(73)90377-1
  2. Dubois. M., Gilles, K. A., Hamilton, J. K., Rebers, P. A. and Smith, F. (1956) Colorimetric method for determination of sugars and related substances. Anal. Chem. 28, 350-365. https://doi.org/10.1021/ac60111a017
  3. Gonzalez. R., Dunkel, R., Koletzko, B., Schusdziarra. V. and Allescher, H. D. (1998) Effects of capsaicin-containing red pepper sauce suspension on upper gastrointestinal motility in healthy volunteers. Dig. Dis. Sci. 43, 1165-1171. https://doi.org/10.1023/A:1018831018566
  4. lino. K., Ohno. N., Susuki. I., Miyazaki. T. and Yadomae, T. (1985) Structural characterization of a neutral antitumor $\beta$-D-glucan extracted with hot sodium hydroxide from cultured fruit bodies of Grifola frondosa. Carbohydr. Res. 141, 111-119. https://doi.org/10.1016/S0008-6215(00)90760-2
  5. Jones, Y. M. and Albersheim, P. O. (1972) A gas chromatographic method for the determination of aldose and uronic acid constituents of plant cell wall polysaccharide. Plant Physiol. 49. 926-936. https://doi.org/10.1104/pp.49.6.926
  6. Kabat, E. A. and Mayer. M. M. (1964) Complement and complement fixation: in Experimental Immunology, Charles C. Thomas Publisher, Springfield, Illinois.
  7. Kiyohara, H., Cyong, J.-C. and Yamada, H. (1989) Relationship between structure and activity of an anti-complementary arabinogalactan from the roots of Angelica acutiloba Kitagawa. Carbohydr. Res. 193, 193-200. https://doi.org/10.1016/0008-6215(89)85118-3
  8. Kojima, Y., Schibukawa, N., Mizunoe, K., Otsuka, K. and Kumazawa, Y. (1980) Screening for interferon inducers and mitogens among various medicinal plants used in traditional Sino-Japanese medicine. Proc. Symp. WAKAN-YAKU. 13, 101-106.
  9. Kumazawa, Y., Mizunoe, K. and Otsuka, Y. (1982) Immunostimulating polysaccharide separated from hot water extract of Angelica acutiloba Kitagawa (Yamato Tohki). Immunology 47, 75-81.
  10. Lee, J. C. and Lim, K. T. (2001) Inhibitory effects of the ethanol extract of ulmus davidiana on apoptosis induced by glucose- glucose oxidase and cytokine production in cultured mouse primary immune cells. J. Biochem. Mol. Biol. 34, 463-471.
  11. Morrison, D. C. and Jacobs. D. M. (1976) Inhibition of lipopolysaccharide initiated activation of serum complement by polymyxin B. infect. Immunol. 13, 298-301.
  12. Park, K. A., Kweon, S. and Choi, H. (2002) Anticarcinogenic effect and modification of cytochrome P450 2E1 by dietary garlic powder in diethylnitrosamine-initiated rat hepatocarcinogenesis. J. Biochem. Mol. Biol. 35, 615-622. https://doi.org/10.5483/BMBRep.2002.35.6.615
  13. Ra, K. S., Yamada, H., Sung. H. J., Cyong, J.-C. and Yang, H. C. (1989) Purification and chemical properties of anti- complementary polysaccharide from Capsid fructus. J. Korean Agri. Chem. Soc. 32. 378-385.
  14. Ra, K. S., Lee, B. L., Lee, H. S. and Kweon, M. H. (1997) Anti-coagulant polysaccharide isolated from Ganoderma lucidum. Korean J. Food & Nutr. 10, 375-381.
  15. Rose. G. D. (ed.) (1986) lmmunobiology of the complement system. An introduction for research and clinical medicine. Academic Press, Orlando.
  16. Samuelsen. A. B., Lund, I., Djahromi, J. M., Paulsen, B. S., Wold, J. K. and Knutsen, S. H. (1999) Structural features and anti-complementary activity of some heteroxylan polysaccharide fractions from the seeds of Plantago major L. Carbohydrate Polymers. 38, 133-143. https://doi.org/10.1016/S0144-8617(98)00115-5
  17. Toda, N., Usui. H., Nishino, N. and Fugiwara, M. (1972) Cardiovascular effects of capsaicin in dogs and rabbits. J. Pharmac. Exp. Ther. 181, 512-521.
  18. Ukai, S., Kiho, T., Hara, C., Kuruma, I. and Yushiro, Y. (1983) Polysaccharide in fungi. XIV. Anti-inflammatory effect of the polysaccharides from the fruit bodies of several fungi. J. Pharmac. Dyn. 6. 983-990. https://doi.org/10.1248/bpb1978.6.983
  19. Wilson, M. E. and Morrison, D. C. (1982) Evidence for different requirements in physical state for the interaction of lipopolysaccharides with the classical and alternative pathways of complement. Eur. J. Biochem. 128, 137-141.
  20. Yamada, H., Kiyohara, H., Cyong, J-C., Kojima, Y., Kumazawa, Y. and Otsuka, Y. (1985) Studies on polysaccharides from Angelica acutiloba. Malec. lmmunol. 22, 295-304. https://doi.org/10.1016/0161-5890(85)90165-8
  21. Yamada, H., Ra, K. S., Kiyohara, H., Cyong, J-C., Yang, H. C. and Otsuka, Y. (1988) Characterization of anti-complementary neutral polysaccharide from the roots of Bupleurum falcatum. Phytochemistry 27, 3163-3168. https://doi.org/10.1016/0031-9422(88)80020-7
  22. Yamada, H., Ra, K. S., Kiyohara, H., Cyong. J-C., Yang, H. C. and Otsuka, Y. (1989) Structural characterization of an anti-complementary pectic polysaccharide from the roots of Bupleurum falcatum. Carbohydr. Res. 189, 209-226. https://doi.org/10.1016/0008-6215(89)84098-4
  23. Yamada, H., Kiyohara, H., Cyong, J-C., Takemoto, N., Komatsu, Y., Kawamura, H., Aburada, M. and Hosoya, E. (1990) Fractionation and characterization of mitogenic and anti- complementary active fractions from Kampo (Japanese herbal) medicine "Juzen-Taiho-To". Planta Med. 56, 386-391. https://doi.org/10.1055/s-2006-960990
  24. Yamada, H., Sun, X. B., Matsumoto, T., Ra, K. S., Hirano, M. and Kiyohara, H. (1991) Purification of anti-ulcer polysaccharide from the roots of Bupleurum falcatum L. Planta Med. 57, 555-559. https://doi.org/10.1055/s-2006-960205
  25. Zhao, J. F., Kiyohara, H., Yamada, H., Takemoto, N. and Kawamura, H. (1991) Heterogeneity and characterization of mitogenic anti-complementary pectic polysaccharides from the roots of Glycyrrhiza uralensis. Carhohydr. Res. 219, 149-172. https://doi.org/10.1016/0008-6215(91)89049-L
  26. Zhao, J. F., Kiyohra, H., Matsumoto, T. and Yamada, H. (1993) Anti-complementary acidic polysaccharides from roots of Lithospermum euchrumum. Phytochemistry 34, 719-724. https://doi.org/10.1016/0031-9422(93)85346-S

Cited by

  1. Pectin isolated from white cabbage – structure and complement-fixing activity vol.50, pp.8, 2006, https://doi.org/10.1002/mnfr.200600026
  2. Chemical composition and anti-inflammatory activity of a pectic polysaccharide isolated from sweet pepper using a simulated gastric medium vol.124, pp.1, 2011, https://doi.org/10.1016/j.foodchem.2010.06.038
  3. Immune-modulating activities of polysaccharides extracted from brown algaeHizikia fusiforme vol.79, pp.8, 2015, https://doi.org/10.1080/09168451.2015.1018121
  4. Immunoregulatory actions of polysaccharides from Chinese herbal medicine vol.14, pp.12, 2010, https://doi.org/10.1517/14728222.2010.531010
  5. Glycoproteins Contained within Soamsan, a Traditional Oriental Medicine, are the Main Class of Active Ingredients Responsible for the Medicine-induced Immune Stimulation vol.38, pp.2, 2005, https://doi.org/10.5483/BMBRep.2005.38.2.253
  6. Isolation and Analysis of Bioactive Compounds inCapsicumPeppers vol.55, pp.2, 2015, https://doi.org/10.1080/10408398.2011.652316
  7. Structural investigation of a heteropolysaccharide isolated from the green fruits of Capsicum annuum vol.344, pp.9, 2009, https://doi.org/10.1016/j.carres.2009.04.004