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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...

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Autores principales: Riebel, A., Dudek, H. M., de Gonzalo, G., Stepniak, P., Rychlewski, L., Fraaije, M. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
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.
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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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