Specialization of Sesquiterpene Lactone Metabolites in <i>Liriodendron</i> Plant Defense

Tulip trees (<i>Liriodendron tulipifera</i> and <i>Liriodendron chinense</i>), members of the Magnolia family, are known for their distinctive morphology and ecological significance, but their chemical diversity remains understudied. In this study, we report the identification and characterization of an array of sesquiterpene lactones (SQLs) produced by <i>L. tulipifera</i>. Through comprehensive chemical analysis, including high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy, we identified a series of STLs with distinct bioactivity profiles. Notably, one of these compounds exhibited antibacterial activity but was only present in <i>L. tulipifera</i>, being absent in <i>L. chinense</i>. Additionally, some STLs demonstrated significant deterrent effects on herbivory or increased mortality, supporting their role as chemical defenses against grazing organisms. These findings provide new insight into the ecological and chemical functions of <i>Liriodendron</i>, highlighting this group's capacity to produce complex bioactive metabolites that may have pharmaceutical and agricultural applications. Our results also suggest that sesquiterpene lactones could be central to the plant's adaptive strategies following evolutionary differentiation with species-specific production of certain metabolites. This work opens new avenues for the exploration of natural products with antimicrobial and herbivore-deterrent properties, with implications for both natural product chemistry and agrochemical lead development.

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Journal
Journal of Natural Products
Published
2025-07-14
DOI
https://doi.org/10.1021/acs.jnatprod.5c00620
Primary Topic
Sesquiterpenes and Asteraceae Studies
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article
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article

Specialization of Sesquiterpene Lactone Metabolites in Liriodendron Plant Defense

David Rowley, Matthew J. Bertin, Kathryn M. Ramsey, Divita Mathur et al.
Journal of Natural Products
Sesquiterpenes and Asteraceae Studies
article

Specialization of Sesquiterpene Lactone Metabolites in Liriodendron Plant Defense

David Rowley, Matthew J. Bertin, Kathryn M. Ramsey, Divita Mathur, Shiwei Chen, Era Srivastava, Sarah Al Kinani, Oli Horyn, Colin Galliano
article en

Abstract

Tulip trees (<i>Liriodendron tulipifera</i> and <i>Liriodendron chinense</i>), members of the Magnolia family, are known for their distinctive morphology and ecological significance, but their chemical diversity remains understudied. In this study, we report the identification and characterization of an array of sesquiterpene lactones (SQLs) produced by <i>L. tulipifera</i>. Through comprehensive chemical analysis, including high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy, we identified a series of STLs with distinct bioactivity profiles. Notably, one of these compounds exhibited antibacterial activity but was only present in <i>L. tulipifera</i>, being absent in <i>L. chinense</i>. Additionally, some STLs demonstrated significant deterrent effects on herbivory or increased mortality, supporting their role as chemical defenses against grazing organisms. These findings provide new insight into the ecological and chemical functions of <i>Liriodendron</i>, highlighting this group's capacity to produce complex bioactive metabolites that may have pharmaceutical and agricultural applications. Our results also suggest that sesquiterpene lactones could be central to the plant's adaptive strategies following evolutionary differentiation with species-specific production of certain metabolites. This work opens new avenues for the exploration of natural products with antimicrobial and herbivore-deterrent properties, with implications for both natural product chemistry and agrochemical lead development.

Journal of Natural ProductsVol. 88(7)
University of Louisville (US), University of Rhode Island (US), University of Louisville Hospital (US), Pharmaceutical Biotechnology (Czechia) (CZ), Case Western Reserve University (US)
Zero hunger
Openalex Percentile: Top 77%
Sesquiterpenes and Asteraceae Studies
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