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Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases
We report enzymes from the berberine bridge enzyme (BBE) superfamily that catalyze the oxidative cyclization of the monoterpene moiety in cannabigerolic acid (CBGA) to form cannabielsoin (CBE). The enzymes are from a variety of organisms and are previously uncharacterized. Out of 232 homologues chos...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9862763/ https://www.ncbi.nlm.nih.gov/pubmed/36674774 http://dx.doi.org/10.3390/ijms24021259 |
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author | Go, Maybelle Kho Zhu, Tingting Lim, Kevin Jie Han Hartono, Yossa Dwi Xue, Bo Fan, Hao Yew, Wen Shan |
author_facet | Go, Maybelle Kho Zhu, Tingting Lim, Kevin Jie Han Hartono, Yossa Dwi Xue, Bo Fan, Hao Yew, Wen Shan |
author_sort | Go, Maybelle Kho |
collection | PubMed |
description | We report enzymes from the berberine bridge enzyme (BBE) superfamily that catalyze the oxidative cyclization of the monoterpene moiety in cannabigerolic acid (CBGA) to form cannabielsoin (CBE). The enzymes are from a variety of organisms and are previously uncharacterized. Out of 232 homologues chosen from the enzyme superfamily, four orthologues were shown to accept CBGA as a substrate and catalyze the biosynthesis of CBE. The four enzymes discovered in this study were recombinantly expressed and purified in Pichia pastoris. These enzymes are the first report of heterologous expression of BBEs that did not originate from the Cannabis plant that catalyze the production of cannabinoids using CBGA as substrate. This study details a new avenue for discovering and producing natural and unnatural cannabinoids. |
format | Online Article Text |
id | pubmed-9862763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98627632023-01-22 Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases Go, Maybelle Kho Zhu, Tingting Lim, Kevin Jie Han Hartono, Yossa Dwi Xue, Bo Fan, Hao Yew, Wen Shan Int J Mol Sci Communication We report enzymes from the berberine bridge enzyme (BBE) superfamily that catalyze the oxidative cyclization of the monoterpene moiety in cannabigerolic acid (CBGA) to form cannabielsoin (CBE). The enzymes are from a variety of organisms and are previously uncharacterized. Out of 232 homologues chosen from the enzyme superfamily, four orthologues were shown to accept CBGA as a substrate and catalyze the biosynthesis of CBE. The four enzymes discovered in this study were recombinantly expressed and purified in Pichia pastoris. These enzymes are the first report of heterologous expression of BBEs that did not originate from the Cannabis plant that catalyze the production of cannabinoids using CBGA as substrate. This study details a new avenue for discovering and producing natural and unnatural cannabinoids. MDPI 2023-01-09 /pmc/articles/PMC9862763/ /pubmed/36674774 http://dx.doi.org/10.3390/ijms24021259 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Go, Maybelle Kho Zhu, Tingting Lim, Kevin Jie Han Hartono, Yossa Dwi Xue, Bo Fan, Hao Yew, Wen Shan Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases |
title | Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases |
title_full | Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases |
title_fullStr | Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases |
title_full_unstemmed | Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases |
title_short | Cannabinoid Biosynthesis Using Noncanonical Cannabinoid Synthases |
title_sort | cannabinoid biosynthesis using noncanonical cannabinoid synthases |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9862763/ https://www.ncbi.nlm.nih.gov/pubmed/36674774 http://dx.doi.org/10.3390/ijms24021259 |
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