Chemistry of Natural Compounds

, Volume 45, Issue 1, pp 1–5 | Cite as

Polysaccharides and sterols from green algae Caulerpa lentillifera and C. sertularioides

  • N. M. Shevchenko
  • Yu. V. Burtseva
  • T. N. Zvyagintseva
  • T. N. Makar′eva
  • O. S. Sergeeva
  • A. M. Zakharenko
  • V. V. Isakov
  • Nguyen Thi Linh
  • Nguyen Xuan Hoa
  • Bui Minh Ly
  • Pham Van Huyen
Article

Sterols and polysaccharides of green alga Caulerpa lentillifera grown under laboratory conditions and in mariculture and polysaccharides of green alga C. sertularioides grown under natural conditions were studied. The sterol fraction consisted of C27-C29 steroidal alcohols with Δ5-unsaturation in the steroid core regardless of the growth conditions. The dominant (79.9%) steroid component of the sterol fraction was clionasterol. The water-soluble fraction of C. lentillifera grown under laboratory conditions was a mixture of 1,4-α- and 1,3-β-D-glucans and protein. The same fraction isolated from C. lentillifera grown in mariculture contained only protein. The water-soluble fraction of C. sertularioides grown under natural conditions contained 1,3;1,6-β-D-galactan sulfated at C2. The principal components of the base-soluble polysaccharide fractions from all algae samples were 1,4-α-D-glucans.

Key words

green algae Caulerpa lentillifera C. sertularioides polysaccharides sterols clionasterol 

Notes

Acknowledgment

The work was supported financially by grants of the RFBR 07-04-90010-viet-a, FEB RAS, and RAS Presidium Program “Cellular and Molecular Biology.”

References

  1. 1.
    P. Ghosh, U. Adhikari, P. Ghosal, C. Pujol, M. Carlucci, E. Damonte, and B. Ray, Phytochemistry, 65, 3151 (2004).PubMedCrossRefGoogle Scholar
  2. 2.
    J.-B. Lee, K. Hayashi, M. Maeda, and T. Hayashi, Planta Med., 70, 813 (2004).PubMedCrossRefGoogle Scholar
  3. 3.
    M. Maeda, T. Uehara, N. Harada, M. Sekiguchi, and A. Hiraoka, Phytochemistry, 30, 3611 (1991).CrossRefGoogle Scholar
  4. 4.
    N. Noda, H. Amano, K. Arashime, and K. Nisizwa, Hydrobilogia, 204/205, 577 (1990).CrossRefGoogle Scholar
  5. 5.
    I. Rubinstein, L. J. Goad, A. D. H. Clague, and L. J. Mulheirn, Phytochemistry, 15, 195 (1976).CrossRefGoogle Scholar
  6. 6.
    T. N. Makarieva, I. A. Bondarenko, A. S. Dmitrenok, V. M. Boguslavsky, V. A. Stonik, V. I. Chernih, and S. M. Efremova, J. Nat. Prod., 54, 953 (1991).CrossRefGoogle Scholar
  7. 7.
    L. DeNapoli, S. Magno, L. Mayol, and E. Novellino, Phytochemistry, 21, 1993 (1982).CrossRefGoogle Scholar
  8. 8.
    N. I. Shevyakova, Fiziol. Rast., 3, 768 (1983).Google Scholar
  9. 9.
    T. N. Zvyagintseva, N. I. Shirokova, and L. A. Elyakova, Bioorg. Khim., 20, 1349 (1994).Google Scholar
  10. 10.
    R. J. Howard, S. W. Wright, and B. R. Grant, Plant Physiol., 58, 459 (1976).PubMedCrossRefGoogle Scholar
  11. 11.
    A. K. Siddhanta, M. Shanmugam, K. H. Mody, A. M. Goswami, and B. K. Ramavat, Int. J. Biol. Macromol., 26, 151 (1999).PubMedCrossRefGoogle Scholar
  12. 12.
    E. V. Rao, N. V. Rao, and K. S. Ramana, Phytochemistry, 30, 1183 (1991).PubMedCrossRefGoogle Scholar
  13. 13.
    M. I. Bilan, A. A. Grachev, N. E. Ustuzhanina, A. S. Shashkov, N. E. Nifantiev, and A. I. Usov, Carbohydr. Res., 337, 719 (2002).PubMedCrossRefGoogle Scholar
  14. 14.
    K. Chattopadhyay, U. Adhikari, P. Lerouge, and B. Ray, Carbohydr. Polym., 68, 407 (2007).CrossRefGoogle Scholar
  15. 15.
    M. I. Bilan, E. V. Vinogradova, A. S. Shashkov, and A. I. Usov, Carbohydr. Res., 342, 586 (2007).PubMedCrossRefGoogle Scholar
  16. 16.
    T. J. Painter, Pure Appl. Chem., 55, 677 (1983).CrossRefGoogle Scholar
  17. 17.
    A. M. Shtaub, in: Methods of Carbohydrate Chemistry [Russian translation], N. K. Kochetkov, ed., Mir, Moscow (1967), 261.Google Scholar
  18. 18.
    M. Dubois, K. A. Gilles, J. K. Hamilton, P. A. Robers, and F. Smith, Anal. Chem., 28, 350 (1956).CrossRefGoogle Scholar
  19. 19.
    M. Bradford, Anal. Biochem., 72, 248 (1976).PubMedCrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, Inc. 2009

Authors and Affiliations

  • N. M. Shevchenko
    • 1
  • Yu. V. Burtseva
    • 1
  • T. N. Zvyagintseva
    • 1
  • T. N. Makar′eva
    • 1
  • O. S. Sergeeva
    • 1
  • A. M. Zakharenko
    • 1
  • V. V. Isakov
    • 1
  • Nguyen Thi Linh
    • 2
  • Nguyen Xuan Hoa
    • 2
  • Bui Minh Ly
    • 3
  • Pham Van Huyen
    • 3
  1. 1.Pacific Institute of Bioorganic Chemistry, Far-East BranchRussian Academy of SciencesVladivostokRussia
  2. 2.Institute of OceanographyVietnamese Academy of Science and TechnologyNhatrangVietnam
  3. 3.Nhatrang Institute of Technology Research and ApplicationVietnamese Academy of Science and TechnologyNhatrangVietnam

Personalised recommendations