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Adsorption of Protamine and Papain Proteins on Saponite

Published online by Cambridge University Press:  01 January 2024

Tamás Szabó
Affiliation:
Department of Colloid Chemistry and Supramolecular and Nanostructured Materials Reseach Group of the Hungarian Academy of Sciences, University of Szeged, Aradi vértanúk tere 1, H-6720 Szeged, Hungary Center for Surface Chemistry and Catalysis, K.U. Leuven, Kasteelpark Arenberg 23, 3001 Leuven, Belgium
Raluca Mitea
Affiliation:
Center for Surface Chemistry and Catalysis, K.U. Leuven, Kasteelpark Arenberg 23, 3001 Leuven, Belgium
Hugo Leeman
Affiliation:
Center for Surface Chemistry and Catalysis, K.U. Leuven, Kasteelpark Arenberg 23, 3001 Leuven, Belgium
Gnanasiri S. Premachandra
Affiliation:
Department of Crop, Soil and Environmental Sciences and Birck Nanotechnology Center, Purdue University, 915 West State Street, West-Lafayette, Indiana 47907-2054, USA
Cliff T. Johnston
Affiliation:
Department of Crop, Soil and Environmental Sciences and Birck Nanotechnology Center, Purdue University, 915 West State Street, West-Lafayette, Indiana 47907-2054, USA
Márta Szekeres
Affiliation:
Department of Colloid Chemistry and Supramolecular and Nanostructured Materials Reseach Group of the Hungarian Academy of Sciences, University of Szeged, Aradi vértanúk tere 1, H-6720 Szeged, Hungary
Imre Dékány
Affiliation:
Department of Colloid Chemistry and Supramolecular and Nanostructured Materials Reseach Group of the Hungarian Academy of Sciences, University of Szeged, Aradi vértanúk tere 1, H-6720 Szeged, Hungary
Robert A. Schoonheydt*
Affiliation:
Center for Surface Chemistry and Catalysis, K.U. Leuven, Kasteelpark Arenberg 23, 3001 Leuven, Belgium
*
* E-mail address of corresponding author: Robert.Schoonheydt@biw.kuleuven.be
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Abstract

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Due to the increased importance of bionanocomposites, protamine and papain proteins were adsorbed on Na+- and on Cs+-exchanged saponite from aqueous solution. Protein analysis of equilibrium solutions and thermogravimetric analyses of biocomposites were used to prepare adsorption isotherms. Based on the isotherm shape, and on the amounts of protein adsorbed and the amounts of Na+ and Cs+ released, the initial protein sorption apparently was due to ion exchange. Additional sorbed protein was weakly retained and could be removed by washing with water. From ion exchange, the average charge of the protamine adsorbed was estimated to be +13.1 to +13.5. Similar papain measurements could not be made due to partial decomposition. Quantitatively, protamine was adsorbed at levels up to 400 mg/g on Na+-saponite and 200 mg/g on Cs+-saponite. The maximum protamine adsorption was 650 to 700 mg/g for Na+-saponite and 350–400 mg/g for Cs+-saponite. Protamine was sorbed to edge surfaces and the basal spacing of the interlamellar region of saponite was 1.75 nm. Protamine displaced only 36% of the Cs+ in Cs+-saponite and expanded the interlamellar region by 36% for a basal spacing of 1.6 nm. Papain sorption to Na+-saponite occurred by a two-step process: (1) adsorption to saponite particle external surfaces followed, (2) by partial intercalation. Quantitatively, Papain was adsorbed up to 100 mg/g for Na+-and Cs+-saponite. Greater initial papain concentrations resulted in a 450 mg/g maximum for Na+-saponite, but no increase above 100 mg/g for Cs+-saponite. Papain apparently only sorbed to external Cs+-saponite surfaces that were estimated to be 33–40 m2/g. Step-wise thermal decomposition of the saponite-protein composites occurred between 300 and 800°C.

Type
Article
Copyright
Copyright © The Clay Minerals Society 2009

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