Skip to main content
Log in

Characterization of organic matrix components of pearl oyster, Pinctada fucata and their implications in shell formation

  • Research Article
  • Published:
Frontiers of Materials Science in China Aims and scope Submit manuscript

Abstract

Mollusks make their shells by biomineralization using Ca2+ and CO3 2− from natural environment. In molluscan shells, two types of CaCO3 crystal which are aragonite and calcite form the species-dependent microstructures. It is believed that shell organic matrices act for control of the crystal types and microstructures. Shell of Pinctada fucata is divided into aragonitic nacreous layer and calcitic prismtic layer. In the recent years, several novel matrix components have been identified in pearl oyster shells by subsequent solubilization of the insoluble matrix, even in the nacreous layer which abounds in the data. In them, we focused our attention on a component, of which the N-terminal amino acid sequence was determined, and attempted cloning genes encoding it. As a result, several clones with typical sequence for the ORF (open reading frame) region were identified and the amino acid sequences were deduced. Further analysis of northern hybridization clarified the tissue specific expressions of the transcripts of the identified genes.

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.

Similar content being viewed by others

References

  1. Watabe N, Wilber K M. Influence of the organic matrix on crystal type in mollusks. Nature, 1960, 188(4747): 334

    Article  Google Scholar 

  2. Lowenstam H A. Minerals formed by organisms. Science, 1981, 211(4487): 1126

    Article  CAS  Google Scholar 

  3. Weiner S. Organization of organic matrix components in mineralized tissues. Integrative & Comparative Biology, 1984, 24(4): 945

    Article  CAS  Google Scholar 

  4. Miyamoto H, Miyashita T, Okushima M, et al. A carbonic anhydrase from the nacreous layer in oyster pearls. Proceedings of the National Academy of Sciences of the United States of America, 1996, 93(18): 9657

    Article  CAS  Google Scholar 

  5. Samata T, Hayashi N, Kono M, et al. A new matrix protein family related to the nacreous layer formation of Pinctada fucata. FEBS Letters, 1999, 462(1): 225–229

    Article  CAS  Google Scholar 

  6. Sudo S, Fujikawa T, Nagakura T, et al. Structures of mollusc shell framework proteins. Nature, 1997, 387(6642): 563–564

    Article  CAS  Google Scholar 

  7. Suzuki M, Murayama E, Inoue H, et al. Characterization of prismalin-14, a novel matrix protein from the prismatic layer of the Japanese pearl oyster (Pinctada fucata). The Biochemical Journal, 2004, 382(1): 205–213

    Article  CAS  Google Scholar 

  8. Tsukamoto D, Sarashina I, Endo K. Structure and expression of an unusually acidic matrix protein of pearl oyster shells. Biochemical and Biophysical Research Communications, 2004, 320(4): 1175–1180

    Article  CAS  Google Scholar 

  9. Gotliv B, Kessler N, Sumerel J L, et al. Asprich: a novel aspartic acid-rich protein family from the prismatic shell matrix of the bivalve Atrina rigida. ChemBioChem, 2005, 6(2): 304–314

    Article  CAS  Google Scholar 

  10. Sarashina I, Endo K. Complete primary structure of the molluscan shell protein 1 (MSP-1) of the scallop Patinopecten yessoensis. Marine Biotechnology, 2001, 3(4): 362–369

    Article  CAS  Google Scholar 

  11. Yano M, Nagai K, Morimoto K, et al. Shematrin: A family of glycine-rich structural proteins in the shell of the pearl oyster Pinctada fucata. Comparative of Biochemistry and Physiology Part B, 2006, 144(2): 254–262

    Article  Google Scholar 

  12. Katoh-Fukui Y, Noce T, Ueda T, et al. The corrected structure of the SM50 spicule matrix protein of Strongylocentrotus purpuratus. Developmental Biology, 1991, 145(1): 201–202

    Article  CAS  Google Scholar 

  13. Katoh-Fukui Y, Noce T, Ueda T, et al. Isolation and characterization of cDNA encoding a spicule matrix protein in Hemicentrotus pulcherrimus micromeres. The International Journal of Developmental Biology, 1992, 36(3): 353–361

    CAS  Google Scholar 

  14. Brandhorst B P, Davenport R. Skeletogenesis in sea urchin interordinal hybrid embryos. Cell and Tissue Research, 2001, 305(1): 159–167

    Article  CAS  Google Scholar 

  15. Peled-Kamar M, Hamilton P, Wilt F H. Spicule matrix protein LSM34 is essential for biomineralization of the sea urchin spicule. Experimental Cell Research, 2002, 272(1): 56–61

    Article  CAS  Google Scholar 

  16. Harkey M A, Klueg K, Sheppard P, et al. Structure, expression, and extracellular targeting of PM27, a skeletal protein associated specifically with growth of the sea urchin larval spicule. Developmental Biology, 1995, 168(2): 549–566

    Article  CAS  Google Scholar 

  17. Raman V, Andrews M E, Harkey M A, et al. Protein-DNA interactions at putative regulatory regions of two coordinately expressed genes, mspl30 and PM27, during skeletogenesis in sea urchin embryos. The International Journal of Developmental Biology, 1993, 37(4): 499–507

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tetsuro Samata.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nogawa, C., Obara, M., Ozawa, M. et al. Characterization of organic matrix components of pearl oyster, Pinctada fucata and their implications in shell formation. Front. Mater. Sci. China 2, 156–161 (2008). https://doi.org/10.1007/s11706-008-0026-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11706-008-0026-4

Keywords

Navigation