Activation and Stabilization of Olive Recombinant 13-Hydroperoxide Lyase Using Selected Additives |
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Authors: | Sabrina Jacopini Sophie Vincenti Magali Mariani Virginie Brunini-Bronzini de Caraffa Claude Gambotti Jean-Marie Desjobert Alain Muselli Jean Costa Félix Tomi Liliane Berti Jacques Maury |
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Affiliation: | 1.Laboratoire de Biochimie et Biologie Moléculaire Végétales,Université de Corse, CNRS UMR6134 SPE,Corte,France;2.Laboratoire de Chimie des Produits Naturels,Université de Corse, CNRS UMR6134 SPE,Corte,France;3.Equipe Chimie et Biomasse,Université de Corse, CNRS UMR6134 SPE,Ajaccio,France |
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Abstract: | The stabilization of olive recombinant hydroperoxide lyases (rHPLs) was investigated using selected chemical additives. Two rHPLs were studied: HPL full-length and HPL with its chloroplast transit peptide deleted (matured HPL). Both olive rHPLs are relatively stable at 4 °C, and enzyme activity can be preserved (about 100% of the rHPL activities are maintained) during 5 weeks of storage at ?20 or at ?80 °C in the presence of glycerol (10%, v/v). Among the additives used in this study, glycine (2.5% w/v), NaCl (0.5 M), and Na2SO4 (0.25 M) provided the highest activation of HPL full-length activity, while the best matured HPL activity was obtained with Na2SO4 (0.25 M) and NaCl (1 M). Although the inactivation rate constants (k) showed that these additives inactivate both rHPLs, their use is still relevant as they strongly increase HPL activity. Results of C6-aldehyde production assays also showed that glycine, NaCl, and Na2SO4 are appropriate additives and that NaCl appears to be the best additive, at least for hexanal production. |
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