Planta Med 2023; 89(08): 833-847
DOI: 10.1055/a-2074-9186
Natural Product Chemistry & Analytical Studies
Original Papers

Overexpression and RNAi-mediated Knockdown of Two 3β-hydroxy-Δ5-steroid dehydrogenase Genes in Digitalis lanata Shoot Cultures Reveal Their Role in Cardenolide Biosynthesis[*]

1   Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
,
Jan Klein
2   Department of Plant Physiology, Friedrich-Schiller-Universität Jena, Germany
,
Mona Ernst
1   Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
,
Maja Dorfner
1   Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
,
Anastasiia Ignatova
1   Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
,
1   Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
,
Harald Lanig
3   National High Performance Computing Center (NHR@FAU), Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
,
1   Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
› Author Affiliations

We are very thankful for the financial support of this study by a grant from the Dr. Hertha and Helmuth Schmauser-Stiftung (JM) and FAU Unibund Anschubfinanzierung (JM).
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Abstract

3β-hydroxy-Δ5-steroid dehydrogenases (3βHSDs) are supposed to be involved in -cardenolide biosynthesis. Here, a novel 3βHSD (Dl3βHSD2) was isolated from Digitalis lanata shoot cultures and expressed in E. coli. Recombinant Dl3βHSD1 and Dl3βHSD2 shared 70% amino acid identity, reduced various 3-oxopregnanes and oxidised 3-hydroxypregnanes, but only rDl3βHSD2 converted small ketones and secondary alcohols efficiently. To explain these differences in substrate specificity, we established homology models using borneol dehydrogenase of Salvia rosmarinus (6zyz) as the template. Hydrophobicity and amino acid residues in the binding pocket may explain the difference in enzyme activities and substrate preferences. Compared to Dl3βHSD1, Dl3βHSD2 is weakly expressed in D. lanata shoots. High constitutive expression of Dl3βHSDs was realised by Agrobacterium-mediated transfer of Dl3βHSD genes fused to the CaMV-35S promotor into the genome of D. lanata wild type shoot cultures. Transformed shoots (35S:Dl3βHSD1 and 35S:Dl3βHSD2) accumulated less cardenolides than controls. The levels of reduced glutathione (GSH), which is known to inhibit cardenolide formation, were higher in the 35S:Dl3βHSD1 lines than in the controls. In the 35S:Dl3βHSD1 lines cardenolide levels were restored after adding of the substrate pregnane-3,20-dione in combination with buthionine-sulfoximine (BSO), an inhibitor of GSH formation. RNAi-mediated knockdown of the Dl3βHSD1 yielded several shoot culture lines with strongly reduced cardenolide levels. In these lines, cardenolide biosynthesis was fully restored after addition of the downstream precursor pregnan-3β-ol-20-one, whereas upstream precursors such as progesterone had no effect, indicating that no shunt pathway could overcome the Dl3βHSD1 knockdown. These results can be taken as the first direct proof that Dl3βHSD1 is indeed involved in -cardenolide biosynthesis.

* Dedicated to Prof. Gerhard Franz, University of Regensburg, Germany, on the occasion of his 85th birthday.


Supporting Information



Publication History

Received: 11 November 2022

Accepted after revision: 31 March 2023

Article published online:
15 May 2023

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