An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells

Whole cells of the yeast Rhodotorula minuta were used in the biotransformation of dialkyl esters of 2-oxoglutaric acid. Almost 100% of conversion with 97-98% of enantiomeric excess of the (S) form of 2-hydroxydiesters was obtained through an enantioselective reduction of dimethyl and diethyl 2-oxogl...

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Autores principales: Rustoy, E., Cerrutti, P., Galvagno, M., Baldessari, A.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_10242422_v26_n3_p204_Rustoy
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spelling todo:paper_10242422_v26_n3_p204_Rustoy2023-10-03T15:56:52Z An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells Rustoy, E. Cerrutti, P. Galvagno, M. Baldessari, A. Biotransformation Dialkyl 2-oxoglutaric acid esters Rhodotorula minuta Cells Enantiomers Enantioselectivity Yeast Biotransformation Dialkyl esters Oxoglutaric acid Esters 2 oxoglutaric acid 4 hydroxybutyric acid article biocatalyst biotransformation decarboxylation enantiomer enantioselectivity hydrolysis nonhuman reduction Rhodotorula Rhodotorula minuta Rhodotorula minuta Whole cells of the yeast Rhodotorula minuta were used in the biotransformation of dialkyl esters of 2-oxoglutaric acid. Almost 100% of conversion with 97-98% of enantiomeric excess of the (S) form of 2-hydroxydiesters was obtained through an enantioselective reduction of dimethyl and diethyl 2-oxoglutarate. When longer alkoxy chain 2-oxoglutarates were used as substrates, the corresponding 4-hydroxybutyric esters were obtained, suggesting a combination process including hydrolysis, decarboxylation and reduction. The cells showed a remarkable high productivity: high conversion and enantiomeric excess were obtained at 2 g wet weight mmol-1 substrate. Fil:Rustoy, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cerrutti, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Galvagno, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Baldessari, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_10242422_v26_n3_p204_Rustoy
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Biotransformation
Dialkyl 2-oxoglutaric acid esters
Rhodotorula minuta
Cells
Enantiomers
Enantioselectivity
Yeast
Biotransformation
Dialkyl esters
Oxoglutaric acid
Esters
2 oxoglutaric acid
4 hydroxybutyric acid
article
biocatalyst
biotransformation
decarboxylation
enantiomer
enantioselectivity
hydrolysis
nonhuman
reduction
Rhodotorula
Rhodotorula minuta
Rhodotorula minuta
spellingShingle Biotransformation
Dialkyl 2-oxoglutaric acid esters
Rhodotorula minuta
Cells
Enantiomers
Enantioselectivity
Yeast
Biotransformation
Dialkyl esters
Oxoglutaric acid
Esters
2 oxoglutaric acid
4 hydroxybutyric acid
article
biocatalyst
biotransformation
decarboxylation
enantiomer
enantioselectivity
hydrolysis
nonhuman
reduction
Rhodotorula
Rhodotorula minuta
Rhodotorula minuta
Rustoy, E.
Cerrutti, P.
Galvagno, M.
Baldessari, A.
An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells
topic_facet Biotransformation
Dialkyl 2-oxoglutaric acid esters
Rhodotorula minuta
Cells
Enantiomers
Enantioselectivity
Yeast
Biotransformation
Dialkyl esters
Oxoglutaric acid
Esters
2 oxoglutaric acid
4 hydroxybutyric acid
article
biocatalyst
biotransformation
decarboxylation
enantiomer
enantioselectivity
hydrolysis
nonhuman
reduction
Rhodotorula
Rhodotorula minuta
Rhodotorula minuta
description Whole cells of the yeast Rhodotorula minuta were used in the biotransformation of dialkyl esters of 2-oxoglutaric acid. Almost 100% of conversion with 97-98% of enantiomeric excess of the (S) form of 2-hydroxydiesters was obtained through an enantioselective reduction of dimethyl and diethyl 2-oxoglutarate. When longer alkoxy chain 2-oxoglutarates were used as substrates, the corresponding 4-hydroxybutyric esters were obtained, suggesting a combination process including hydrolysis, decarboxylation and reduction. The cells showed a remarkable high productivity: high conversion and enantiomeric excess were obtained at 2 g wet weight mmol-1 substrate.
format JOUR
author Rustoy, E.
Cerrutti, P.
Galvagno, M.
Baldessari, A.
author_facet Rustoy, E.
Cerrutti, P.
Galvagno, M.
Baldessari, A.
author_sort Rustoy, E.
title An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells
title_short An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells
title_full An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells
title_fullStr An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells
title_full_unstemmed An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells
title_sort efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by rhodotorula minuta whole cells
url http://hdl.handle.net/20.500.12110/paper_10242422_v26_n3_p204_Rustoy
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