Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone
The enzymatic preparation of a monoacetyl derivative of the corticosteroid cortexolone, through a transesterification reaction, is described. The heterologous Rhizopus oryzae lipase, immobilized on three different supports, proved to be an efficient catalyst in the acylation reaction using a complex...
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todo:paper_1434193X_v_n23_p4306_Quintana2023-10-03T16:14:17Z Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone Quintana, P.G. Guillén, M. Marciello, M. Valero, F. Palomo, J.M. Baldessari, A. Acylation Biocatalysis Enzymes Immobilization Steroids Supported catalysts The enzymatic preparation of a monoacetyl derivative of the corticosteroid cortexolone, through a transesterification reaction, is described. The heterologous Rhizopus oryzae lipase, immobilized on three different supports, proved to be an efficient catalyst in the acylation reaction using a complex substrate such as cortexolone. Immobilization of the enzyme on Lewatit 1600 resin at pH = 7 and 25 °C was the best condition for catalysis of the acetylation reaction. The influence of various reaction parameters, such as the nature of the acetylating agent, the solvent, the temperature, and the ratios of acetylating agent to substrate, and enzyme to substrate, was evaluated. Using the response surface methodology and a central composite rotatable design, the specific yield of acetylated cortexolone was optimized by means of the study of the effect of the enzyme (E)/substrate (S) and the acylating agent (A)/substrate ratios. The ratios of 5 (E/S) and 31.6 (A/S) were predicted as the optimal values to reach the maximum specific yield of the product (P): 1.59 mmol P/mmol A·g E. The mild reaction conditions and low environmental impact make the biocatalytic procedure a convenient way to prepare the reported derivative of this biologically active steroid. The regioselective acetylation of cortexolone was achieved by using an immobilized heterologous Rhizopus oryzae lipase. The mild reaction conditions and low environmental impact make the biocatalytic procedure a convenient way to prepare the monoacetyl derivative of this biologically active steroid. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_1434193X_v_n23_p4306_Quintana |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Acylation Biocatalysis Enzymes Immobilization Steroids Supported catalysts |
| spellingShingle |
Acylation Biocatalysis Enzymes Immobilization Steroids Supported catalysts Quintana, P.G. Guillén, M. Marciello, M. Valero, F. Palomo, J.M. Baldessari, A. Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone |
| topic_facet |
Acylation Biocatalysis Enzymes Immobilization Steroids Supported catalysts |
| description |
The enzymatic preparation of a monoacetyl derivative of the corticosteroid cortexolone, through a transesterification reaction, is described. The heterologous Rhizopus oryzae lipase, immobilized on three different supports, proved to be an efficient catalyst in the acylation reaction using a complex substrate such as cortexolone. Immobilization of the enzyme on Lewatit 1600 resin at pH = 7 and 25 °C was the best condition for catalysis of the acetylation reaction. The influence of various reaction parameters, such as the nature of the acetylating agent, the solvent, the temperature, and the ratios of acetylating agent to substrate, and enzyme to substrate, was evaluated. Using the response surface methodology and a central composite rotatable design, the specific yield of acetylated cortexolone was optimized by means of the study of the effect of the enzyme (E)/substrate (S) and the acylating agent (A)/substrate ratios. The ratios of 5 (E/S) and 31.6 (A/S) were predicted as the optimal values to reach the maximum specific yield of the product (P): 1.59 mmol P/mmol A·g E. The mild reaction conditions and low environmental impact make the biocatalytic procedure a convenient way to prepare the reported derivative of this biologically active steroid. The regioselective acetylation of cortexolone was achieved by using an immobilized heterologous Rhizopus oryzae lipase. The mild reaction conditions and low environmental impact make the biocatalytic procedure a convenient way to prepare the monoacetyl derivative of this biologically active steroid. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
| format |
JOUR |
| author |
Quintana, P.G. Guillén, M. Marciello, M. Valero, F. Palomo, J.M. Baldessari, A. |
| author_facet |
Quintana, P.G. Guillén, M. Marciello, M. Valero, F. Palomo, J.M. Baldessari, A. |
| author_sort |
Quintana, P.G. |
| title |
Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone |
| title_short |
Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone |
| title_full |
Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone |
| title_fullStr |
Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone |
| title_full_unstemmed |
Immobilized heterologous Rhizopus Oryzae lipase as an efficient catalyst in the acetylation of cortexolone |
| title_sort |
immobilized heterologous rhizopus oryzae lipase as an efficient catalyst in the acetylation of cortexolone |
| url |
http://hdl.handle.net/20.500.12110/paper_1434193X_v_n23_p4306_Quintana |
| work_keys_str_mv |
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1807321429833678848 |