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A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis
BACKGROUND: Baeyer-Villiger monooxygenases (BVMOs) represent a group of enzymes of considerable biotechnological relevance as illustrated by their growing use as biocatalyst in a variety of synthetic applications. However, due to their increased use the reproducible expression of BVMOs and other bio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404926/ https://www.ncbi.nlm.nih.gov/pubmed/22720747 http://dx.doi.org/10.1186/1472-6750-12-31 |
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author | van Bloois, Edwin Dudek, Hanna M Duetz, Wouter A Fraaije, Marco W |
author_facet | van Bloois, Edwin Dudek, Hanna M Duetz, Wouter A Fraaije, Marco W |
author_sort | van Bloois, Edwin |
collection | PubMed |
description | BACKGROUND: Baeyer-Villiger monooxygenases (BVMOs) represent a group of enzymes of considerable biotechnological relevance as illustrated by their growing use as biocatalyst in a variety of synthetic applications. However, due to their increased use the reproducible expression of BVMOs and other biotechnologically relevant enzymes has become a pressing matter while knowledge about the factors governing their reproducible expression is scattered. RESULTS: Here, we have used phenylacetone monooxygenase (PAMO) from Thermobifida fusca, a prototype Type I BVMO, as a model enzyme to develop a stepwise strategy to optimize the biotransformation performance of recombinant E. coli expressing PAMO in 96-well microtiter plates in a reproducible fashion. Using this system, the best expression conditions of PAMO were investigated first, including different host strains, temperature as well as time and induction period for PAMO expression. This optimized system was used next to improve biotransformation conditions, the PAMO-catalyzed conversion of phenylacetone, by evaluating the best electron donor, substrate concentration, and the temperature and length of biotransformation. Combining all optimized parameters resulted in a more than four-fold enhancement of the biocatalytic performance and, importantly, this was highly reproducible as indicated by the relative standard deviation of 1% for non-washed cells and 3% for washed cells. Furthermore, the optimized procedure was successfully adapted for activity-based mutant screening. CONCLUSIONS: Our optimized procedure, which provides a comprehensive overview of the key factors influencing the reproducible expression and performance of a biocatalyst, is expected to form a rational basis for the optimization of miniaturized biotransformations and for the design of novel activity-based screening procedures suitable for BVMOs and other NAD(P)H-dependent enzymes as well. |
format | Online Article Text |
id | pubmed-3404926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34049262012-07-26 A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis van Bloois, Edwin Dudek, Hanna M Duetz, Wouter A Fraaije, Marco W BMC Biotechnol Research Article BACKGROUND: Baeyer-Villiger monooxygenases (BVMOs) represent a group of enzymes of considerable biotechnological relevance as illustrated by their growing use as biocatalyst in a variety of synthetic applications. However, due to their increased use the reproducible expression of BVMOs and other biotechnologically relevant enzymes has become a pressing matter while knowledge about the factors governing their reproducible expression is scattered. RESULTS: Here, we have used phenylacetone monooxygenase (PAMO) from Thermobifida fusca, a prototype Type I BVMO, as a model enzyme to develop a stepwise strategy to optimize the biotransformation performance of recombinant E. coli expressing PAMO in 96-well microtiter plates in a reproducible fashion. Using this system, the best expression conditions of PAMO were investigated first, including different host strains, temperature as well as time and induction period for PAMO expression. This optimized system was used next to improve biotransformation conditions, the PAMO-catalyzed conversion of phenylacetone, by evaluating the best electron donor, substrate concentration, and the temperature and length of biotransformation. Combining all optimized parameters resulted in a more than four-fold enhancement of the biocatalytic performance and, importantly, this was highly reproducible as indicated by the relative standard deviation of 1% for non-washed cells and 3% for washed cells. Furthermore, the optimized procedure was successfully adapted for activity-based mutant screening. CONCLUSIONS: Our optimized procedure, which provides a comprehensive overview of the key factors influencing the reproducible expression and performance of a biocatalyst, is expected to form a rational basis for the optimization of miniaturized biotransformations and for the design of novel activity-based screening procedures suitable for BVMOs and other NAD(P)H-dependent enzymes as well. BioMed Central 2012-06-21 /pmc/articles/PMC3404926/ /pubmed/22720747 http://dx.doi.org/10.1186/1472-6750-12-31 Text en Copyright ©2012 van Bloois et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article van Bloois, Edwin Dudek, Hanna M Duetz, Wouter A Fraaije, Marco W A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis |
title | A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis |
title_full | A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis |
title_fullStr | A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis |
title_full_unstemmed | A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis |
title_short | A stepwise approach for the reproducible optimization of PAMO expression in Escherichia coli for whole-cell biocatalysis |
title_sort | stepwise approach for the reproducible optimization of pamo expression in escherichia coli for whole-cell biocatalysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404926/ https://www.ncbi.nlm.nih.gov/pubmed/22720747 http://dx.doi.org/10.1186/1472-6750-12-31 |
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