Skip to main content
Log in

Three Types of Acidic Polysaccharides Associated with Coccolith of Pleurochrysis haptonemofera: Comparison with Pleurochrysis carterae and Analysis Using Fluorescein-Isothiocyanate-Labeled Lectins

  • Published:
Marine Biotechnology Aims and scope Submit manuscript

Abstract

In the coccolithophorid microalgae acidic polysaccharides are considered to be involved in the formation of the calcified scale, coccolith. Characteristics of the acidic polysaccharides extracted from the cell surface of the coccolithophorid Pleurochrysis haptonemofera were analyzed. The acidic polysaccharides on the cell surface can be detected by measuring fluorescence of cells after fluorescein-isothiocyanate-labeled lectin staining by flow cytometry. Flow cytometric analyses revealed that the acidic polysaccharides remained on the cell surface even after CaCO3 in the coccolith was dissolved by lowering pH, but they were extracted by subsequent EDTA or EGTA treatment, suggesting that they are bound not into the CaCO3 crystals of the coccolith, but onto the surface via Ca2+. Analyses of the acidic polysaccharides by anion exchange chromatography, colloidal precipitation with divalent cations, and polyacrylamide gel electrophoresis (PAGE) revealed that P. haptonemofera has 3 types of acidic polysaccharides (Ph-PS-l, -2, and -3). The PAGE patterns suggested that Ph-PS-2 has a repeated structure with a broad range of molecular weight, as in Pleurochrysis carterae, while Ph-PS-1 and -3 contain several minor components in addition to a major component, respectively. The minor components in Ph-PS-1 and -3 that have not been found in P. carterae might be characteristic of P. haptonemofera. Analyses of both the cell surface treated by various concentrations of EDTA and EGTA and the extracts suggested that Ph-PS-2, which is distinguishable by a higher affinity to concanavalin A, is bound onto the coccolith surface more intensely than the other two types of acidic polysaccharides.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Bitter T, Muir HM (1962) A modified uronic acid carbazole reaction. Anal Biochem 4: 330–034

    Article  Google Scholar 

  • Borman AH, de long EW, Huizinga M, Kok DJ, Westbroak P, Bosch L (1982) The role in CaCO3 crystallization of an acid Ca2+ -binding polysaccharide associated with coccoliths of Emiliania huxleyi. Eur J Biochem 129: 179–483

    Article  Google Scholar 

  • Fichtinger-Shepman AMJ, Kamerling JR, Vliegenthart JFG (1981) Composition of a methylated, acidic polysaccharide associated with coccoliths of Emiliania huxleyi (Lohmann) Kamptner. Carbohydr Res 69: 181–189

    Google Scholar 

  • Fujiwara S, Iwahashi H, Someya J, Nishikawa S, Minaka N (1993) Structure and cotranscription of the plastid-encoded rbcL and rbcS genes of Pleurochrysis carterae (Prymnesiophyta). J Phycol 29: 347–355

    Article  Google Scholar 

  • Fujiwaraj S, Sawada M, Someya J, Minaka N, Kawachi M, Inouye I (1994). Molecular phylogenetic analysis of rbcL in the Prymnesiophyta. J Phycol 30: 863–871

    Article  Google Scholar 

  • Fujiwara S, Kawachi M, Minaka N, Inouye I (2001) Molecular phylogeny of the Haptophyta based on the rbcL gene and sequence variation in the spacer region on the rubisco operon. J Phycol 37: 121–129

    Article  Google Scholar 

  • Green JC, Leadbeater BSC (1994) The Haptophyta Algae. Systematic Association Special Volume. Oxford, U.K.: Clarendon Press, 51

    Google Scholar 

  • Green MR, Pastewka JV, Peacock A (1973). Differential staining of phosphoproteins on polyacrylamide gels with a cationic carbocyanine dye. Anal Biochem 56: 43–51

    Article  Google Scholar 

  • Inoue H, Ozaki N, Nagasawa H (2001) Purification and structural determination of a phosphorylated peptide with anti-calcification and chitin-binding activities in the exoskeleton of the crayfish, Procambams clarkii. Biosci Biotechnol Biochem 65: 1840–1848

    Google Scholar 

  • Inoue H, Ohira T, Ozaki N, Nagasawa H (2004) A novel calcium-binding peptide from the cuticle of the crayfish Procambarus clarkii. Biochem Biophys Res Commun 318: 649–654

    Article  Google Scholar 

  • Inouye I, Chihara M (1979) Life history and taxonomy of Cricosphaera roscoffensis var. haptonemofera, var. nov. (class Prymnesiophyceae) from the Pacific. Bot Mag Tokyo 92: 75–87

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680–685

    Article  Google Scholar 

  • Marsh ME, (1986) Biomineralization in the presence of calcium-binding phosphoprotein particles. J Exp Zool 239: 207–220

    Article  Google Scholar 

  • Marsh ME (1994) Polyanion-mediated mineralization — assembly and recognization of acidic polysaccharides in the Golgi system of a coccolithophorid alga during mineral deposition. Protoplasma 177: 108–122

    Article  Google Scholar 

  • Marsh ME (1996) Polyanion-mediated mineralization — a kinetic analysis of the calcium-carrier hypothesis in the phytoflagellate Pleurochrysis carterae. Protoplasma 190: 181–188

    Article  Google Scholar 

  • Marsh ME (2000) Polyanion in the CaCO3 mineralization of coccolithophores. In: Bauerlein E, (ed.)Biomineralization: From Biology to Biotechnology and Medical Application, Weinheim, Germany: Wiley-VCH 251–268

    Google Scholar 

  • Marsh ME, Dickinson DP, (1997) Polyanion-mediated mineralization — mineralization in coccolithophore (Pleurochrysis carterae) variants which do not express PS2, the most abundant and acidic mineral-associated polyanion in wild-type cells. Protoplasma 199: 9–17

    Google Scholar 

  • Marsh ME, Sass RJL (1984) Calcium–binding phosphoprotein particles in the extrapallial fluid and innermost shell lamella of clams. J Exp Zool 226: 193–203

    Google Scholar 

  • Marsh ME, Chang DK, King GC (1992) Isolation and characterization of a novel acidic polysaccharide containing tartrate and glyoxylate residues from the mineralized scales of a unicellular coccolithophorid alga, Pleurochrysis carterae. J Biol Chem 267: 20507–20512

    Google Scholar 

  • Marsh ME, Ridall AL, Azadi P, Duke RJ (2002) Galacturonomannan and Golgi-derived membrane linked to growth and shaping of biogenic calcite. J Struct Biol 139: 39–45

    Article  Google Scholar 

  • Miyamoto T, Miyashita T, Okushima M, Nakano S, Morita T, Matsushiro A (1996) A carbonic anhydrase from the nacreous layer in oyster pearls. Proc Natl Acad Sci U S A 93: 9657–9660

    Article  Google Scholar 

  • Murayama E, Okuno A, Ohira T, Nagasawa H (2000) Molecular cloning and expression of an otolith matrix protein cDNA from the rainbow trout, Oncorhynchus mykiss. Comp Biochem Physiol 126B: 511–520

    Google Scholar 

  • Murayama E, Takagi Y, Ohira T, Davis JG, Greene MI, Nagasawa H (2002) Fish otolith contains a unique structural protein, otolin-1. Eur J Biochem 269: 688–696

    Article  Google Scholar 

  • Okazaki M (1992) Algal calcification: its contribution to the “CO2 problem”. Korean J Phycol 7: 147–154

    Google Scholar 

  • Okazaki M, Sato T, Mutho N, Wada N, Umegaki T (1998) Calcified scales (coccolith) of Pleurochrysis carterae (Haptophyta): structure, crystallography, and acid polysaccharides. J Mar Biotechnol 6: 16–22

    Google Scholar 

  • Ozaki N, Sakuda S, Nagasawa H (2001). Isolation and some characterization of an acidic polysaccharide with anti-calcification activity from coccoliths of a marine alga, Pleurochrysis carterae. Biosci Biotechnol Biochem 65: 2330–2333

    Article  Google Scholar 

  • Ozaki N, Okazaki M, Kogure T, Sakuda S, Nagasawa H (2004) Structural and functional diversity of acidic polysaccharides from various species of coccolithophorid algae. Thalassas 20: 61–70

    Google Scholar 

  • Sekino K, Shiraiwa Y (1996) Evidence for the involvement of mitochondorial respiration in calcification in a marine coccolithophorid. Plant Cell Physiol 37: 1030–1033

    Google Scholar 

  • Shiraiwa Y (2003) Physiological regulation of carbon fixation in the photosynthesis and calcification of coccolithophorids. Comp Biochem Physiol B Biochem Mol Biol 136: 775–783

    Google Scholar 

  • Takahashi J, Fujiwara S, Kikyo M, Hirokawa Y, Tsuzuki M (2002) Discrimination of the cell surface of the coccolithophorid Pleurochrysis haptonemofera from light scattering and fluorescein-isothiocyanate-labeled lectin staining measured by flow cytometry. Mar Biotechnol 4: 94–101

    Article  Google Scholar 

  • van Bleijwijk J, van der Wal P, Kemper R, Veldhuis M, Young JR, Muyzer G, de Vrind-de Jong E, Westbroek P. (1991) Distribution of two types of Emiliania huxleyi (Prymnesiophyceae) in the Northeast Atlantic region as determined by immunofluorescene and coccolith morphology. J Phycol 27: 566–570

    Google Scholar 

  • van der Wal P, de Jong EW, Westbroek R, de Bruijin WC, Mulder-Stapel AA, (1983) Polysaccharide localization, coccolith formation and Golgi dynamics in the coccolithophorid Hymenomonas carterae. J Ultrastr Res 85: 139–158

    Google Scholar 

  • van Emburg PR, de Jong EW, Daems W. Th. (1986) Immunological localization of a polysaccharide from biomineral structures (coccoliths) of Emiliania huxleyi. J Ultrastr Molecul Struc Res 94: 246–259

    Google Scholar 

  • Watanabe MM, Kasai R, Sudo R (1988) NIES-Collection List of Strains, 2nd ed. Microalgae and Protozoa. Tsukuba, Japan: Microbial Culture Collection, The National Institute for Environmental Studies, 163

    Google Scholar 

  • Winter A, Siesser WG (1994) Coccolithophores. Cambridge, U.K.: Cambridge University Press

    Google Scholar 

  • Young JR, Westbroek P (1991) Genotypic variation in the coccolithophorid species Emiliania huxleyi. Mar Micropalaentol 18: 5–23

    Google Scholar 

Download references

Acknowledgments

The authors thank Dr. I. Inouye of Tsukuba University, Japan, for providing the P. haptonemofera cells, and Dr. H Nagasawa and Dr. N. Ozaki of University of Tokyo, as well as Dr. M. Okazaki of Tokyo Gakugei University, for their helpful comments and encouragements. This work was supported by Grant-in-Aid from the Ministry of Education, Science, Sports, and Cultures, Japan (13640657), the Promotion and Mutual Aid Corporation for Private Schools of Japan, and a Sasakawa Scientific Research Grant from The Japan Science Society to Y.H.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mikio Tsuzuki.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hirokawa, Y., Fujiwara, S. & Tsuzuki, M. Three Types of Acidic Polysaccharides Associated with Coccolith of Pleurochrysis haptonemofera: Comparison with Pleurochrysis carterae and Analysis Using Fluorescein-Isothiocyanate-Labeled Lectins. Mar Biotechnol 7, 634–644 (2005). https://doi.org/10.1007/s10126-004-5148-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10126-004-5148-9

Keywords

Navigation