Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase

A lipase-catalyzed preparation of ethyl and stearyl esters of chenodeoxycholic acid is described. Stearyl chenodeoxycholate is a new product and both bile acid esters were prepared through an enzymatic approach for the first time. The heterologous Rhizopus oryzae lipase, immobilized on two different...

Full description

Bibliographic Details
Published in:Journal of Molecular Catalysis B: Enzymatic
Main Authors: Quintana, Paula Gabriela, Canet, Albert, Marciello, Marzia, Valero, Francisco, Palomo, José M., Baldessari, Alicia
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier Science
Subjects:
Online Access:http://hdl.handle.net/11336/18722
_version_ 1821772083470794752
author Quintana, Paula Gabriela
Canet, Albert
Marciello, Marzia
Valero, Francisco
Palomo, José M.
Baldessari, Alicia
author_facet Quintana, Paula Gabriela
Canet, Albert
Marciello, Marzia
Valero, Francisco
Palomo, José M.
Baldessari, Alicia
author_sort Quintana, Paula Gabriela
collection CONICET Digital (Consejo Nacional de Investigaciones Científicas y Técnicas)
container_start_page 36
container_title Journal of Molecular Catalysis B: Enzymatic
container_volume 118
description A lipase-catalyzed preparation of ethyl and stearyl esters of chenodeoxycholic acid is described. Stearyl chenodeoxycholate is a new product and both bile acid esters were prepared through an enzymatic approach for the first time. The heterologous Rhizopus oryzae lipase, immobilized on two different supports proved to be an efficient catalyst, even more active than Candida antarctica lipase, in the esterification reaction using a complex substrate such as a bile acid. The immobilization of the enzyme on Octadecyl Sepabeads at pH 7 and 25 °C was the best choice to catalyze the esterification reaction. The influence of various reaction parameters, such as nature of the alcohol, alcohol:substrate ratio, enzyme:substrate ratio, solvent and temperature, was evaluated. Using the response surface methodology and a central composite rotatable design, the conversion of stearyl chenodeoxycholate was optimized by means of the study of the effect of enzyme:substrate ratio and alcohol:substrate ratio. The value 20 for ratios (E/S) and (A/S) was predicted as the optimal value to reach the maximum conversion. However, including economic aspects these ratios can be reduced up to 15. The well-known advantages of biocatalysis and the activity shown by the immobilized heterologous lipase make the reported procedure a convenient way to prepare chenodeoxycholic esters. Fil: Quintana, Paula Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos en Química Orgánica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Unidad de Microanálisis y Métodos Físicos en Química Orgánica; Argentina Fil: Canet, Albert. Universitat Autònoma de Barcelona; España Fil: Marciello, Marzia. Consejo Superior de Investigaciones Científicas. Instituto de Catalisis y Petroleoquímica; España Fil: Valero, Francisco. Universitat Autònoma de Barcelona; España Fil: Palomo, José M. Consejo Superior de Investigaciones ...
format Article in Journal/Newspaper
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
geographic Argentina
geographic_facet Argentina
id ftconicet:oai:ri.conicet.gov.ar:11336/18722
institution Open Polar
language English
op_collection_id ftconicet
op_container_end_page 42
op_doi https://doi.org/10.1016/j.molcatb.2015.05.008
op_relation info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molcatb.2015.05.008
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1381117715001332
http://hdl.handle.net/11336/18722
Quintana, Paula Gabriela; Canet, Albert; Marciello, Marzia; Valero, Francisco; Palomo, José M.; et al.; Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase; Elsevier Science; Journal of Molecular Catalysis B: Enzymatic; 118; 8-2015; 36-42
1381-1177
CONICET Digital
CONICET
op_rights info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
publisher Elsevier Science
record_format openpolar
spelling ftconicet:oai:ri.conicet.gov.ar:11336/18722 2025-01-16T19:38:48+00:00 Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase Quintana, Paula Gabriela Canet, Albert Marciello, Marzia Valero, Francisco Palomo, José M. Baldessari, Alicia application/pdf http://hdl.handle.net/11336/18722 eng eng Elsevier Science info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molcatb.2015.05.008 info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1381117715001332 http://hdl.handle.net/11336/18722 Quintana, Paula Gabriela; Canet, Albert; Marciello, Marzia; Valero, Francisco; Palomo, José M.; et al.; Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase; Elsevier Science; Journal of Molecular Catalysis B: Enzymatic; 118; 8-2015; 36-42 1381-1177 CONICET Digital CONICET info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ Chenodeoxycholic Acid Esters Enzyme-Catalyzed Rhizopus Oryzae Lipase Immobilization https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion ftconicet https://doi.org/10.1016/j.molcatb.2015.05.008 2023-09-24T19:02:55Z A lipase-catalyzed preparation of ethyl and stearyl esters of chenodeoxycholic acid is described. Stearyl chenodeoxycholate is a new product and both bile acid esters were prepared through an enzymatic approach for the first time. The heterologous Rhizopus oryzae lipase, immobilized on two different supports proved to be an efficient catalyst, even more active than Candida antarctica lipase, in the esterification reaction using a complex substrate such as a bile acid. The immobilization of the enzyme on Octadecyl Sepabeads at pH 7 and 25 °C was the best choice to catalyze the esterification reaction. The influence of various reaction parameters, such as nature of the alcohol, alcohol:substrate ratio, enzyme:substrate ratio, solvent and temperature, was evaluated. Using the response surface methodology and a central composite rotatable design, the conversion of stearyl chenodeoxycholate was optimized by means of the study of the effect of enzyme:substrate ratio and alcohol:substrate ratio. The value 20 for ratios (E/S) and (A/S) was predicted as the optimal value to reach the maximum conversion. However, including economic aspects these ratios can be reduced up to 15. The well-known advantages of biocatalysis and the activity shown by the immobilized heterologous lipase make the reported procedure a convenient way to prepare chenodeoxycholic esters. Fil: Quintana, Paula Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos en Química Orgánica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Unidad de Microanálisis y Métodos Físicos en Química Orgánica; Argentina Fil: Canet, Albert. Universitat Autònoma de Barcelona; España Fil: Marciello, Marzia. Consejo Superior de Investigaciones Científicas. Instituto de Catalisis y Petroleoquímica; España Fil: Valero, Francisco. Universitat Autònoma de Barcelona; España Fil: Palomo, José M. Consejo Superior de Investigaciones ... Article in Journal/Newspaper Antarc* Antarctica CONICET Digital (Consejo Nacional de Investigaciones Científicas y Técnicas) Argentina Journal of Molecular Catalysis B: Enzymatic 118 36 42
spellingShingle Chenodeoxycholic Acid Esters
Enzyme-Catalyzed
Rhizopus Oryzae Lipase
Immobilization
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Quintana, Paula Gabriela
Canet, Albert
Marciello, Marzia
Valero, Francisco
Palomo, José M.
Baldessari, Alicia
Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase
title Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase
title_full Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase
title_fullStr Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase
title_full_unstemmed Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase
title_short Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase
title_sort enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous rhizopus oryzae lipase
topic Chenodeoxycholic Acid Esters
Enzyme-Catalyzed
Rhizopus Oryzae Lipase
Immobilization
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
topic_facet Chenodeoxycholic Acid Esters
Enzyme-Catalyzed
Rhizopus Oryzae Lipase
Immobilization
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
url http://hdl.handle.net/11336/18722