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Influence of tryptophan tags on the purification of cutinase, secreted by a recombinant Saccharomyces cerevisiae, using cationic expanded bed adsorption and hydrophobic interaction chromatography

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Abstract

During cationic bed adsorption (EBA), with cutinase with varying length tryptophan tags (WP)2 and (WP)4, 33% and 10% of adsorption capacity and 80% and 32% eluted specific activity were observed in relation to wild type (wt)-cutinase in the conventional process. Therefore, as the hydrophobicity of the protein increases, it is important to integrate the EBA step with a hydrophobic interaction chromatography (HIC) process. As the length of the hydrophobic tag-(WP) increases from n = 2 to n = 4, the purification factor obtained by HIC was 1.8 and 2.2-fold higher than wt-cutinase. However, the recovery yield obtained in HIC decreases substantially as the length of hydrophobic tag increases (97%, 84% and 70% for wt-cutinase, cutinase-(WP)2 and cutinase-(WP)4). The integration of two purification steps, EBA followed by HIC, resulted in the highest overall purity level for cutinase-(WP)2, and the highest overall recovery yield for wt-cutinase. When optimizing the design of a hydrophobic tag fused to a protein secreted by Saccharomyces cerevisiae it must be considered that the cultivation parameters could impair the downstream process, and consequently the optimum tag is not necessarily the one that presents the highest purification factor in HIC.

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Acknowledgments

The authors would like to acknowledge the financial support from the “Programa de Cooperación Científica Internacional” GRICES/CONICYT 2002-6-152,“Proyecto Enlace ENL06/14” of the “Departamento de Investigación Universidad of Chile” and The Institute for Cell Dynamics and Biotechnology—ICBD (project ICM (P05-001-F).

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Correspondence to M. E. Lienqueo.

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Lienqueo, M.E., Salazar, O., Calado, C.R.C. et al. Influence of tryptophan tags on the purification of cutinase, secreted by a recombinant Saccharomyces cerevisiae, using cationic expanded bed adsorption and hydrophobic interaction chromatography. Biotechnol Lett 30, 1353–1358 (2008). https://doi.org/10.1007/s10529-008-9696-3

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  • DOI: https://doi.org/10.1007/s10529-008-9696-3

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