The enzymes OSC1 and CYP716A263 produce a high variety of triterpenoids in the latex of Taraxacum koksaghyz.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
11 04 2019
Historique:
received: 16 07 2018
accepted: 28 03 2019
entrez: 13 4 2019
pubmed: 13 4 2019
medline: 2 10 2020
Statut: epublish

Résumé

Only very little is known about the resin composition of natural rubber from the dandelion species Taraxacum koksaghyz, thus its full characterization could provide new insights into how the isoprenoid end-products influence the physical properties of natural rubber, and this resin might be a good source of highly diverse triterpenoids. Here, we present a comprehensive analysis of the triterpenoid composition in an acetone extract and identified 13 triterpenes and triterpenoids also including the so far unknown pentacyclic compounds lup-19(21)-en-3-ol (1) and its ketone lup-19(21)-en-3-one (2). We purified single triterpenes from the acetone extract by developing a two-step HPLC system that is adapted to the structural differences of the described triterpenoids. Furthermore, we isolated six different oxidosqualene cyclases (OSCs) and two P450 enzymes, and we functionally characterized TkOSC1 and CYP716A263 in Nicotiana benthamiana and Saccharomyces cerevisiae in detail. TkOSC1 is a multifunctional OSC that was capable of synthesizing at least four of the latex-predominant pentacyclic triterpenes (taraxasterol, α-, β-amyrin and lup-19(21)-en-3-ol) while CYP716A263 oxidized pentacyclic triterpenes at the C-3 position. The identified enzymes responsible for biosynthesis and modification of pentacyclic triterpenes in T. koksaghyz latex may represent excellent tools for bioengineering approaches to produce pentacyclic triterpenes heterologously.

Identifiants

pubmed: 30976052
doi: 10.1038/s41598-019-42381-w
pii: 10.1038/s41598-019-42381-w
pmc: PMC6459903
doi:

Substances chimiques

Latex 0
Plant Proteins 0
Triterpenes 0
Cytochrome P-450 Enzyme System 9035-51-2
Intramolecular Transferases EC 5.4.-
lanosterol synthase EC 5.4.99.7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5942

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Auteurs

Katharina M Pütter (KM)

University of Muenster, Institute of Plant Biology and Biotechnology, Schlossplatz 8, 48143, Muenster, Germany.

Nicole van Deenen (N)

University of Muenster, Institute of Plant Biology and Biotechnology, Schlossplatz 8, 48143, Muenster, Germany.

Boje Müller (B)

Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Schlossplatz 8, 48143, Muenster, Germany.

Lea Fuchs (L)

University of Muenster, Institute of Plant Biology and Biotechnology, Schlossplatz 8, 48143, Muenster, Germany.

Kirsten Vorwerk (K)

University of Muenster, Institute of Plant Biology and Biotechnology, Schlossplatz 8, 48143, Muenster, Germany.

Kristina Unland (K)

Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Schlossplatz 8, 48143, Muenster, Germany.

Jan Niklas Bröker (JN)

University of Muenster, Institute of Plant Biology and Biotechnology, Schlossplatz 8, 48143, Muenster, Germany.

Emely Scherer (E)

Technische Universität München, Chair of Biochemistry, Lichtenbergstraße 4, 85747, Garching, Germany.

Claudia Huber (C)

Technische Universität München, Chair of Biochemistry, Lichtenbergstraße 4, 85747, Garching, Germany.

Wolfgang Eisenreich (W)

Technische Universität München, Chair of Biochemistry, Lichtenbergstraße 4, 85747, Garching, Germany.

Dirk Prüfer (D)

University of Muenster, Institute of Plant Biology and Biotechnology, Schlossplatz 8, 48143, Muenster, Germany.
Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Schlossplatz 8, 48143, Muenster, Germany.

Christian Schulze Gronover (C)

Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Schlossplatz 8, 48143, Muenster, Germany. christian.schulze.gronover@ime.fraunhofer.de.

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Classifications MeSH