Expanding the Landscape of Diterpene Structural Diversity through Stereochemically Controlled Combinatorial Biosynthesis
Abstract: Plant‐derived diterpenoids serve as important pharmaceuticals, food additives, and fragrances, yet their low natural abundance and high structural complexity limits their broader industrial utilization. By mimicking the modularity of diterpene biosynthesis in plants, we constructed 51 functional combinations of class I and II diterpene synthases, 41 of which are “new‐to‐nature”. Stereoselective biosynthesis of over 50 diterpene skeletons was demonstrated, including natural variants and novel enantiomeric or diastereomeric counterparts. Scalable biotechnological production for four industrially relevant targets was accomplished in engineered strains of Saccharomyces cerevisiae.
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Expanding the Landscape of Diterpene Structural Diversity through Stereochemically Controlled Combinatorial Biosynthesis ; volume:128 ; number:6 ; year:2016 ; pages:2182-2186 ; extent:5
Angewandte Chemie ; 128, Heft 6 (2016), 2182-2186 (gesamt 5)
- Creator
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Andersen‐Ranberg, Johan
Kongstad, Kenneth Thermann
Nielsen, Morten Thrane
Jensen, Niels Bjerg
Pateraki, Irini
Bach, Søren Spanner
Hamberger, Britta
Zerbe, Philipp
Staerk, Dan
Bohlmann, Jörg
Møller, Birger Lindberg
Hamberger, Björn
- DOI
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10.1002/ange.201510650
- URN
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urn:nbn:de:101:1-2022101106410409480202
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:27 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Andersen‐Ranberg, Johan
- Kongstad, Kenneth Thermann
- Nielsen, Morten Thrane
- Jensen, Niels Bjerg
- Pateraki, Irini
- Bach, Søren Spanner
- Hamberger, Britta
- Zerbe, Philipp
- Staerk, Dan
- Bohlmann, Jörg
- Møller, Birger Lindberg
- Hamberger, Björn