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Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry

Nepetalactones are iridoid monoterpenes with a broad range of biological activities produced by plants in the Nepeta genus. However, none of the genes for nepetalactone biosynthesis have been discovered. Here we report the transcriptomes of two Nepeta species, each with distinctive profiles of nepet...

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Autores principales: Sherden, Nathaniel H., Lichman, Benjamin, Caputi, Lorenzo, Zhao, Dongyan, Kamileen, Mohamed O., Buell, C. Robin, O'Connor, Sarah E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739345/
https://www.ncbi.nlm.nih.gov/pubmed/29091815
http://dx.doi.org/10.1016/j.phytochem.2017.10.004
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author Sherden, Nathaniel H.
Lichman, Benjamin
Caputi, Lorenzo
Zhao, Dongyan
Kamileen, Mohamed O.
Buell, C. Robin
O'Connor, Sarah E.
author_facet Sherden, Nathaniel H.
Lichman, Benjamin
Caputi, Lorenzo
Zhao, Dongyan
Kamileen, Mohamed O.
Buell, C. Robin
O'Connor, Sarah E.
author_sort Sherden, Nathaniel H.
collection PubMed
description Nepetalactones are iridoid monoterpenes with a broad range of biological activities produced by plants in the Nepeta genus. However, none of the genes for nepetalactone biosynthesis have been discovered. Here we report the transcriptomes of two Nepeta species, each with distinctive profiles of nepetalactone stereoisomers. As a starting point for investigation of nepetalactone biosynthesis in Nepeta, these transcriptomes were used to identify candidate genes for iridoid synthase homologs, an enzyme that has been shown to form the core iridoid skeleton in several iridoid producing plant species. Iridoid synthase homologs identified from the transcriptomes were cloned, heterologously expressed, and then assayed with the 8-oxogeranial substrate. These experiments revealed that catalytically active iridoid synthase enzymes are present in Nepeta, though there are unusual mutations in key active site residues. Nevertheless, these enzymes exhibit similar catalytic activity and product profile compared to previously reported iridoid synthases from other plants. Notably, four nepetalactone stereoisomers with differing stereochemistry at the 4α and 7α positions – which are generated during the iridoid synthase reaction – are observed at different ratios in various Nepeta species. This work strongly suggests that the variable stereochemistry at these 4α and 7α positions of nepetalactone diastereomers is established further downstream in the iridoid pathway in Nepeta. Overall, this work provides a gateway into the biosynthesis of nepetalactones in Nepeta.
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spelling pubmed-57393452018-01-02 Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry Sherden, Nathaniel H. Lichman, Benjamin Caputi, Lorenzo Zhao, Dongyan Kamileen, Mohamed O. Buell, C. Robin O'Connor, Sarah E. Phytochemistry Article Nepetalactones are iridoid monoterpenes with a broad range of biological activities produced by plants in the Nepeta genus. However, none of the genes for nepetalactone biosynthesis have been discovered. Here we report the transcriptomes of two Nepeta species, each with distinctive profiles of nepetalactone stereoisomers. As a starting point for investigation of nepetalactone biosynthesis in Nepeta, these transcriptomes were used to identify candidate genes for iridoid synthase homologs, an enzyme that has been shown to form the core iridoid skeleton in several iridoid producing plant species. Iridoid synthase homologs identified from the transcriptomes were cloned, heterologously expressed, and then assayed with the 8-oxogeranial substrate. These experiments revealed that catalytically active iridoid synthase enzymes are present in Nepeta, though there are unusual mutations in key active site residues. Nevertheless, these enzymes exhibit similar catalytic activity and product profile compared to previously reported iridoid synthases from other plants. Notably, four nepetalactone stereoisomers with differing stereochemistry at the 4α and 7α positions – which are generated during the iridoid synthase reaction – are observed at different ratios in various Nepeta species. This work strongly suggests that the variable stereochemistry at these 4α and 7α positions of nepetalactone diastereomers is established further downstream in the iridoid pathway in Nepeta. Overall, this work provides a gateway into the biosynthesis of nepetalactones in Nepeta. Elsevier 2018-01 /pmc/articles/PMC5739345/ /pubmed/29091815 http://dx.doi.org/10.1016/j.phytochem.2017.10.004 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sherden, Nathaniel H.
Lichman, Benjamin
Caputi, Lorenzo
Zhao, Dongyan
Kamileen, Mohamed O.
Buell, C. Robin
O'Connor, Sarah E.
Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
title Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
title_full Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
title_fullStr Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
title_full_unstemmed Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
title_short Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
title_sort identification of iridoid synthases from nepeta species: iridoid cyclization does not determine nepetalactone stereochemistry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739345/
https://www.ncbi.nlm.nih.gov/pubmed/29091815
http://dx.doi.org/10.1016/j.phytochem.2017.10.004
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