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Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening
To expand the available set of Baeyer–Villiger monooxygenases (BVMOs), we have created expression constructs for producing 22 Type I BVMOs that are present in the genome of Rhodococcus jostii RHA1. Each BVMO has been probed with a large panel of potential substrates. Except for testing their substra...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427485/ https://www.ncbi.nlm.nih.gov/pubmed/22218769 http://dx.doi.org/10.1007/s00253-011-3823-0 |
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author | Riebel, A. Dudek, H. M. de Gonzalo, G. Stepniak, P. Rychlewski, L. Fraaije, M. W. |
author_facet | Riebel, A. Dudek, H. M. de Gonzalo, G. Stepniak, P. Rychlewski, L. Fraaije, M. W. |
author_sort | Riebel, A. |
collection | PubMed |
description | To expand the available set of Baeyer–Villiger monooxygenases (BVMOs), we have created expression constructs for producing 22 Type I BVMOs that are present in the genome of Rhodococcus jostii RHA1. Each BVMO has been probed with a large panel of potential substrates. Except for testing their substrate acceptance, also the enantioselectivity of some selected BVMOs was studied. The results provide insight into the biocatalytic potential of this collection of BVMOs and expand the biocatalytic repertoire known for BVMOs. This study also sheds light on the catalytic capacity of this large set of BVMOs that is present in this specific actinomycete. Furthermore, a comparative sequence analysis revealed a new BVMO-typifying sequence motif. This motif represents a useful tool for effective future genome mining efforts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-011-3823-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3427485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-34274852012-08-30 Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening Riebel, A. Dudek, H. M. de Gonzalo, G. Stepniak, P. Rychlewski, L. Fraaije, M. W. Appl Microbiol Biotechnol Biotechnologically Relevant Enzymes and Proteins To expand the available set of Baeyer–Villiger monooxygenases (BVMOs), we have created expression constructs for producing 22 Type I BVMOs that are present in the genome of Rhodococcus jostii RHA1. Each BVMO has been probed with a large panel of potential substrates. Except for testing their substrate acceptance, also the enantioselectivity of some selected BVMOs was studied. The results provide insight into the biocatalytic potential of this collection of BVMOs and expand the biocatalytic repertoire known for BVMOs. This study also sheds light on the catalytic capacity of this large set of BVMOs that is present in this specific actinomycete. Furthermore, a comparative sequence analysis revealed a new BVMO-typifying sequence motif. This motif represents a useful tool for effective future genome mining efforts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-011-3823-0) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-01-05 2012 /pmc/articles/PMC3427485/ /pubmed/22218769 http://dx.doi.org/10.1007/s00253-011-3823-0 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Biotechnologically Relevant Enzymes and Proteins Riebel, A. Dudek, H. M. de Gonzalo, G. Stepniak, P. Rychlewski, L. Fraaije, M. W. Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening |
title | Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening |
title_full | Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening |
title_fullStr | Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening |
title_full_unstemmed | Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening |
title_short | Expanding the set of rhodococcal Baeyer–Villiger monooxygenases by high-throughput cloning, expression and substrate screening |
title_sort | expanding the set of rhodococcal baeyer–villiger monooxygenases by high-throughput cloning, expression and substrate screening |
topic | Biotechnologically Relevant Enzymes and Proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427485/ https://www.ncbi.nlm.nih.gov/pubmed/22218769 http://dx.doi.org/10.1007/s00253-011-3823-0 |
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