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  Biosynthesis of costunolide, dihydrocostunolide, and leucodin. Demonstration of cytochrome P450-catalyzed formation of the lactone ring present in sesquiterpene lactones of chicory

Kraker, D., Franssen, M. C. R., Joerink, M., De Groot, A., & Bouwmeester, H. J. (2002). Biosynthesis of costunolide, dihydrocostunolide, and leucodin. Demonstration of cytochrome P450-catalyzed formation of the lactone ring present in sesquiterpene lactones of chicory. Plant Physiology, 129(1), 257-268. doi:10.1104/pp.010957.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-A53B-8 Version Permalink: https://hdl.handle.net/21.11116/0000-0009-380B-D
Genre: Journal Article

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GER036.pdf (Publisher version), 0B
 
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC155889/ (Publisher version)
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 Creators:
Kraker, De1, Author           
Franssen, M. C. R., Author
Joerink, M., Author
De Groot, A., Author
Bouwmeester, H. J., Author
Affiliations:
1Department of Biochemistry, Prof. J. Gershenzon, MPI for Chemical Ecology, Max Planck Society, Jena, DE, ou_421893              

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Free keywords: Cichorium-intybus; roots; biotransformation; peppermint
 Abstract: Chicory (Cichorium intybus) is known to contain guaianolides, eudesmanolides, and germacranolides. These sesquiterpene lactones are postulated to originate from a common germacranolide, namely (+)-costunolide. Whereas a pathway for the formation of germ

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 Dates: 2002
 Publication Status: Issued
 Pages: -
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 Rev. Type: -
 Identifiers: Other: GER036
DOI: 10.1104/pp.010957
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Title: Plant Physiology
  Other : Plant Physiol.
Source Genre: Journal
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Publ. Info: Bethesda, Md. : American Society of Plant Biologists
Pages: - Volume / Issue: 129 (1) Sequence Number: - Start / End Page: 257 - 268 Identifier: ISSN: 0032-0889
CoNE: https://pure.mpg.de/cone/journals/resource/991042744294438