Cargando…

Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis

Biocatalysis has emerged as an important tool in synthetic organic chemistry enabling the chemical industry to execute reactions with high regio- or enantioselectivity and under usually mild reaction conditions while avoiding toxic waste. Target substrates and products of reactions catalyzed by carb...

Descripción completa

Detalles Bibliográficos
Autores principales: Bollinger, Alexander, Molitor, Rebecka, Thies, Stephan, Koch, Rainhard, Coscolín, Cristina, Ferrer, Manuel, Jaeger, Karl-Erich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170478/
https://www.ncbi.nlm.nih.gov/pubmed/32111588
http://dx.doi.org/10.1128/AEM.00106-20
_version_ 1783523900293906432
author Bollinger, Alexander
Molitor, Rebecka
Thies, Stephan
Koch, Rainhard
Coscolín, Cristina
Ferrer, Manuel
Jaeger, Karl-Erich
author_facet Bollinger, Alexander
Molitor, Rebecka
Thies, Stephan
Koch, Rainhard
Coscolín, Cristina
Ferrer, Manuel
Jaeger, Karl-Erich
author_sort Bollinger, Alexander
collection PubMed
description Biocatalysis has emerged as an important tool in synthetic organic chemistry enabling the chemical industry to execute reactions with high regio- or enantioselectivity and under usually mild reaction conditions while avoiding toxic waste. Target substrates and products of reactions catalyzed by carboxylic ester hydrolases are often poorly water soluble and require organic solvents, whereas enzymes are evolved by nature to be active in cells, i.e., in aqueous rather than organic solvents. Therefore, biocatalysts that withstand organic solvents are urgently needed. Current strategies to identify such enzymes rely on laborious tests carried out by incubation in different organic solvents and determination of residual activity. Here, we describe a simple assay useful for screening large libraries of carboxylic ester hydrolases for resistance and activity in water-miscible organic solvents. We have screened a set of 26 enzymes, most of them identified in this study, with four different water-miscible organic solvents. The triglyceride tributyrin was used as a substrate, and fatty acids released by enzymatic hydrolysis were detected by a pH shift indicated by the indicator dye nitrazine yellow. With this strategy, we succeeded in identifying a novel highly organic-solvent-tolerant esterase from Pseudomonas aestusnigri. In addition, the newly identified enzymes were tested with sterically demanding substrates, which are common in pharmaceutical intermediates, and two enzymes from Alcanivorax borkumensis were identified which outcompeted the gold standard ester hydrolase CalB from Candida antarctica. IMPORTANCE Major challenges hampering biotechnological applications of esterases include the requirement to accept nonnatural and chemically demanding substrates and the tolerance of the enzymes toward organic solvents which are often required to solubilize such substrates. We describe here a high-throughput screening strategy to identify novel organic-solvent-tolerant carboxylic ester hydrolases (CEs). Among these enzymes, CEs active against water-insoluble bulky substrates were identified. Our results thus contribute to fostering the identification and biotechnological application of CEs.
format Online
Article
Text
id pubmed-7170478
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-71704782020-04-27 Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis Bollinger, Alexander Molitor, Rebecka Thies, Stephan Koch, Rainhard Coscolín, Cristina Ferrer, Manuel Jaeger, Karl-Erich Appl Environ Microbiol Biotechnology Biocatalysis has emerged as an important tool in synthetic organic chemistry enabling the chemical industry to execute reactions with high regio- or enantioselectivity and under usually mild reaction conditions while avoiding toxic waste. Target substrates and products of reactions catalyzed by carboxylic ester hydrolases are often poorly water soluble and require organic solvents, whereas enzymes are evolved by nature to be active in cells, i.e., in aqueous rather than organic solvents. Therefore, biocatalysts that withstand organic solvents are urgently needed. Current strategies to identify such enzymes rely on laborious tests carried out by incubation in different organic solvents and determination of residual activity. Here, we describe a simple assay useful for screening large libraries of carboxylic ester hydrolases for resistance and activity in water-miscible organic solvents. We have screened a set of 26 enzymes, most of them identified in this study, with four different water-miscible organic solvents. The triglyceride tributyrin was used as a substrate, and fatty acids released by enzymatic hydrolysis were detected by a pH shift indicated by the indicator dye nitrazine yellow. With this strategy, we succeeded in identifying a novel highly organic-solvent-tolerant esterase from Pseudomonas aestusnigri. In addition, the newly identified enzymes were tested with sterically demanding substrates, which are common in pharmaceutical intermediates, and two enzymes from Alcanivorax borkumensis were identified which outcompeted the gold standard ester hydrolase CalB from Candida antarctica. IMPORTANCE Major challenges hampering biotechnological applications of esterases include the requirement to accept nonnatural and chemically demanding substrates and the tolerance of the enzymes toward organic solvents which are often required to solubilize such substrates. We describe here a high-throughput screening strategy to identify novel organic-solvent-tolerant carboxylic ester hydrolases (CEs). Among these enzymes, CEs active against water-insoluble bulky substrates were identified. Our results thus contribute to fostering the identification and biotechnological application of CEs. American Society for Microbiology 2020-04-17 /pmc/articles/PMC7170478/ /pubmed/32111588 http://dx.doi.org/10.1128/AEM.00106-20 Text en Copyright © 2020 Bollinger et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biotechnology
Bollinger, Alexander
Molitor, Rebecka
Thies, Stephan
Koch, Rainhard
Coscolín, Cristina
Ferrer, Manuel
Jaeger, Karl-Erich
Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis
title Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis
title_full Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis
title_fullStr Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis
title_full_unstemmed Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis
title_short Organic-Solvent-Tolerant Carboxylic Ester Hydrolases for Organic Synthesis
title_sort organic-solvent-tolerant carboxylic ester hydrolases for organic synthesis
topic Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170478/
https://www.ncbi.nlm.nih.gov/pubmed/32111588
http://dx.doi.org/10.1128/AEM.00106-20
work_keys_str_mv AT bollingeralexander organicsolventtolerantcarboxylicesterhydrolasesfororganicsynthesis
AT molitorrebecka organicsolventtolerantcarboxylicesterhydrolasesfororganicsynthesis
AT thiesstephan organicsolventtolerantcarboxylicesterhydrolasesfororganicsynthesis
AT kochrainhard organicsolventtolerantcarboxylicesterhydrolasesfororganicsynthesis
AT coscolincristina organicsolventtolerantcarboxylicesterhydrolasesfororganicsynthesis
AT ferrermanuel organicsolventtolerantcarboxylicesterhydrolasesfororganicsynthesis
AT jaegerkarlerich organicsolventtolerantcarboxylicesterhydrolasesfororganicsynthesis