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

Nathaniel H. Sherden, Benjamin Lichman, Lorenzo Caputi, Dongyan Zhao, Mohamed O. Kamileen, C. Robin Buell, Sarah E. O’Connor
doi: https://doi.org/10.1101/179572
Nathaniel H. Sherden
§Department of Biological Chemistry, The John Innes Centre, Norwich, NR4 7UH UK
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Benjamin Lichman
§Department of Biological Chemistry, The John Innes Centre, Norwich, NR4 7UH UK
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Lorenzo Caputi
§Department of Biological Chemistry, The John Innes Centre, Norwich, NR4 7UH UK
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Dongyan Zhao
¶Department of Plant Biology, Michigan State University, East Lansing, MI, 48824 USA
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Mohamed O. Kamileen
§Department of Biological Chemistry, The John Innes Centre, Norwich, NR4 7UH UK
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C. Robin Buell
¶Department of Plant Biology, Michigan State University, East Lansing, MI, 48824 USA
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Sarah E. O’Connor
§Department of Biological Chemistry, The John Innes Centre, Norwich, NR4 7UH UK
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  • For correspondence: sarah.oconnor@jic.ac.uk
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Iridoid synthase from Nepeta cateria (catnip) and Nepeta mussinii, have been cloned and characterized.

Abstract 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.

Highlights

  • Species within the Nepeta genus (such as catnip) produce nepetalactone iridoids

  • The enzymes that produce the iridoid scaffold of nepetalactone were identified from two species of Nepeta

  • The iridoid synthase enzymes are not responsible for the stereochemical variation in these iridoids

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted August 22, 2017.
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Identification of Iridoid Synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
Nathaniel H. Sherden, Benjamin Lichman, Lorenzo Caputi, Dongyan Zhao, Mohamed O. Kamileen, C. Robin Buell, Sarah E. O’Connor
bioRxiv 179572; doi: https://doi.org/10.1101/179572
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Identification of Iridoid Synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry
Nathaniel H. Sherden, Benjamin Lichman, Lorenzo Caputi, Dongyan Zhao, Mohamed O. Kamileen, C. Robin Buell, Sarah E. O’Connor
bioRxiv 179572; doi: https://doi.org/10.1101/179572

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