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Identification and characterization of piperine synthase from black pepper, Piper nigrum L.
Black pepper (Piper nigrum L.) is the world’s most popular spice and is also used as an ingredient in traditional medicine. Its pungent perception is due to the interaction of its major compound, piperine (1-piperoyl-piperidine) with the human TRPV-1 or vanilloid receptor. We now identify the hither...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032705/ https://www.ncbi.nlm.nih.gov/pubmed/33833371 http://dx.doi.org/10.1038/s42003-021-01967-9 |
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author | Schnabel, Arianne Athmer, Benedikt Manke, Kerstin Schumacher, Frank Cotinguiba, Fernando Vogt, Thomas |
author_facet | Schnabel, Arianne Athmer, Benedikt Manke, Kerstin Schumacher, Frank Cotinguiba, Fernando Vogt, Thomas |
author_sort | Schnabel, Arianne |
collection | PubMed |
description | Black pepper (Piper nigrum L.) is the world’s most popular spice and is also used as an ingredient in traditional medicine. Its pungent perception is due to the interaction of its major compound, piperine (1-piperoyl-piperidine) with the human TRPV-1 or vanilloid receptor. We now identify the hitherto concealed enzymatic formation of piperine from piperoyl coenzyme A and piperidine based on a differential RNA-Seq approach from developing black pepper fruits. This enzyme is described as piperine synthase (piperoyl-CoA:piperidine piperoyl transferase) and is a member of the BAHD-type of acyltransferases encoded by a gene that is preferentially expressed in immature fruits. A second BAHD-type enzyme, also highly expressed in immature black pepper fruits, has a rather promiscuous substrate specificity, combining diverse CoA-esters with aliphatic and aromatic amines with similar efficiencies, and was termed piperamide synthase. Recombinant piperine and piperamide synthases are members of a small gene family in black pepper. They can be used to facilitate the microbial production of a broad range of medicinally relevant aliphatic and aromatic piperamides based on a wide array of CoA-donors and amine-derived acceptors, offering widespread applications. |
format | Online Article Text |
id | pubmed-8032705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80327052021-04-27 Identification and characterization of piperine synthase from black pepper, Piper nigrum L. Schnabel, Arianne Athmer, Benedikt Manke, Kerstin Schumacher, Frank Cotinguiba, Fernando Vogt, Thomas Commun Biol Article Black pepper (Piper nigrum L.) is the world’s most popular spice and is also used as an ingredient in traditional medicine. Its pungent perception is due to the interaction of its major compound, piperine (1-piperoyl-piperidine) with the human TRPV-1 or vanilloid receptor. We now identify the hitherto concealed enzymatic formation of piperine from piperoyl coenzyme A and piperidine based on a differential RNA-Seq approach from developing black pepper fruits. This enzyme is described as piperine synthase (piperoyl-CoA:piperidine piperoyl transferase) and is a member of the BAHD-type of acyltransferases encoded by a gene that is preferentially expressed in immature fruits. A second BAHD-type enzyme, also highly expressed in immature black pepper fruits, has a rather promiscuous substrate specificity, combining diverse CoA-esters with aliphatic and aromatic amines with similar efficiencies, and was termed piperamide synthase. Recombinant piperine and piperamide synthases are members of a small gene family in black pepper. They can be used to facilitate the microbial production of a broad range of medicinally relevant aliphatic and aromatic piperamides based on a wide array of CoA-donors and amine-derived acceptors, offering widespread applications. Nature Publishing Group UK 2021-04-08 /pmc/articles/PMC8032705/ /pubmed/33833371 http://dx.doi.org/10.1038/s42003-021-01967-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Schnabel, Arianne Athmer, Benedikt Manke, Kerstin Schumacher, Frank Cotinguiba, Fernando Vogt, Thomas Identification and characterization of piperine synthase from black pepper, Piper nigrum L. |
title | Identification and characterization of piperine synthase from black pepper, Piper nigrum L. |
title_full | Identification and characterization of piperine synthase from black pepper, Piper nigrum L. |
title_fullStr | Identification and characterization of piperine synthase from black pepper, Piper nigrum L. |
title_full_unstemmed | Identification and characterization of piperine synthase from black pepper, Piper nigrum L. |
title_short | Identification and characterization of piperine synthase from black pepper, Piper nigrum L. |
title_sort | identification and characterization of piperine synthase from black pepper, piper nigrum l. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8032705/ https://www.ncbi.nlm.nih.gov/pubmed/33833371 http://dx.doi.org/10.1038/s42003-021-01967-9 |
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