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Extraction and Purification of Matrix Protein from the Nacre of Pearl Oyster Pinctada fucata

Caiping MA1Cen ZHANG1Yancheng NIE1Liping XIE1,2Rongqing ZHANG1,2( )
Institute of Marine Biotechnology, Department of Biological Sciences and Biotechnology, Tsinghua University, Beijing 100084, China
Protein Science Laboratory of the Ministry of Education, Tsinghua University, Beijing 100084, China
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Abstract

A soluble matrix protein P14 with an apparent molecular mass of 14.5 kDa was isolated from fragmented nacre of pearl oysters (Pinctada fucata) treated with 10% NaOH solution to investigate the nacre matrix proteins and their effect on the CaCO3 crystal. The protein was characterized by gel exclusion chromatography and reversed-phase high performance liquid chromatography after demineralization by 10% acetic acid. The X-ray diffraction pattern of P14 crystals indicates that P14 plays an important role in nacre biomineralization. P14 can induce aragonite formation, stimulate CaCO3 crystal formation, and accelerate aragonite precipitation. Heating of the acid insoluble nacre residue, which was named conchiolin, in 10% sodium dodecyl sulfate solution supplemented with 10% β-mercaptoethanol solution for 10-20 min at about 100°C gave two other soluble proteins having molecular masses of 19.4 kDa and 25.0 kDa. The present study suggests that these two proteins are linked to the insoluble organic matrix by disulfide bridges because the extraction yield increases when β-mercaptoethanol is added to the medium.

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Tsinghua Science and Technology
Pages 499-503

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Cite this article:
MA C, ZHANG C, NIE Y, et al. Extraction and Purification of Matrix Protein from the Nacre of Pearl Oyster Pinctada fucata. Tsinghua Science and Technology, 2005, 10(4): 499-503. https://doi.org/10.1016/S1007-0214(05)70107-3

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Received: 09 December 2004
Revised: 14 January 2005
Published: 01 August 2005
© Tsinghua University Press 2005