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PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization

Penicillin-binding protein-type thioesterases (PBP-type TEs) are a recently identified group of peptide cyclases that catalyze head-to-tail macrolactamization of nonribosomal peptides. PenA, a new member of this group, is involved in the biosyntheses of cyclic pentapeptides. In this study, we demons...

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Detalles Bibliográficos
Autores principales: Matsuda, Kenichi, Fujita, Kei, Wakimoto, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113502/
https://www.ncbi.nlm.nih.gov/pubmed/33713128
http://dx.doi.org/10.1093/jimb/kuab023
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author Matsuda, Kenichi
Fujita, Kei
Wakimoto, Toshiyuki
author_facet Matsuda, Kenichi
Fujita, Kei
Wakimoto, Toshiyuki
author_sort Matsuda, Kenichi
collection PubMed
description Penicillin-binding protein-type thioesterases (PBP-type TEs) are a recently identified group of peptide cyclases that catalyze head-to-tail macrolactamization of nonribosomal peptides. PenA, a new member of this group, is involved in the biosyntheses of cyclic pentapeptides. In this study, we demonstrated the enzymatic activity of PenA in vitro, and analyzed its substrate scope with a series of synthetic substrates. A comparison of the reaction profiles between PenA and SurE, a representative PBP-type TE, showed that PenA is more specialized for small peptide cyclization. A computational model provided a possible structural rationale for the altered specificity for substrate chain lengths.
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spelling pubmed-91135022022-06-08 PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization Matsuda, Kenichi Fujita, Kei Wakimoto, Toshiyuki J Ind Microbiol Biotechnol Biocatalysis Penicillin-binding protein-type thioesterases (PBP-type TEs) are a recently identified group of peptide cyclases that catalyze head-to-tail macrolactamization of nonribosomal peptides. PenA, a new member of this group, is involved in the biosyntheses of cyclic pentapeptides. In this study, we demonstrated the enzymatic activity of PenA in vitro, and analyzed its substrate scope with a series of synthetic substrates. A comparison of the reaction profiles between PenA and SurE, a representative PBP-type TE, showed that PenA is more specialized for small peptide cyclization. A computational model provided a possible structural rationale for the altered specificity for substrate chain lengths. Oxford University Press 2021-03-13 /pmc/articles/PMC9113502/ /pubmed/33713128 http://dx.doi.org/10.1093/jimb/kuab023 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Society of Industrial Microbiology and Biotechnology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Biocatalysis
Matsuda, Kenichi
Fujita, Kei
Wakimoto, Toshiyuki
PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization
title PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization
title_full PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization
title_fullStr PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization
title_full_unstemmed PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization
title_short PenA, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization
title_sort pena, a penicillin-binding protein-type thioesterase specialized for small peptide cyclization
topic Biocatalysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113502/
https://www.ncbi.nlm.nih.gov/pubmed/33713128
http://dx.doi.org/10.1093/jimb/kuab023
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