RSS-Feed abonnieren
DOI: 10.1055/s-2007-981537
© Georg Thieme Verlag KG Stuttgart · New York
Δ5-3β-Hydroxysteroid Dehydrogenase (3βHSD) from Digitalis lanata. Heterologous Expression and Characterisation of the Recombinant Enzyme[*]
Dedicated to Professor A. Wilhelm Alfermann on the occasion of his 65th birthdayPublikationsverlauf
Received: March 7, 2007
Revised: April 24, 2007
Accepted: May 4, 2007
Publikationsdatum:
12. Juni 2007 (online)
Abstract
During the biosynthesis of cardiac glycosides, Δ5-3β-hydroxysteroid dehydrogenase (3βHSD, EC 1.1.1.51) converts pregnenolone (5-pregnen-3β-ol-20-one) to isoprogesterone (5-pregnene-3,20-dione). A 3βHSD gene was isolated from leaves of Digitalis lanata. It consisted of 870 nucleotides containing a 90 nucleotide long intron. A full-length cDNA clone that encodes 3βHSD was isolated by RT-PCR from the same source. A Sph I/Kpn I 3βHSD cDNA was cloned into the pQE30 vector and then transferred into E. coli strain M15[pREP4]. 3βHSD cDNA was functionally expressed as a His-tagged fusion protein (pQ3βHSD) composed of 273 amino acids (calculated molecular mass 28,561 Da). pQ3βHSD was purified by metal chelate affinity chromatography on Ni-NTA. Pregnenolone and other 3β-hydroxypregnanes but not cholesterol were 3β-oxidised by pQ3βHSD when NAD was used as the co-substrate. Testosterone (4-androsten-17β-ol-3-one) was converted to 4-androstene-3,17-dione indicating that the pQ3βHSD has also 17β-dehydrogenase activity. pQ3βHSD was able to reduce 3-keto steroids to their corresponding 3β-hydroxy derivatives when NADH was used as the co-substrate. For comparison, 3βHSD genes were isolated and sequenced from another 6 species of the genus Digitalis. Gene structure and the deduced 3βHSD proteins share a high degree of similarity.
Key words
Δ5-3β-Hydroxysteroid dehydrogenase - Δ5-3-ketosteroid isomerase - Digitalis lanata - cardenolide biosynthesis - gene expression - Plantaginaceae - pregnenolone - progesterone
- Supporting Information for this article is available online at
- Supporting Information .
1 The nucleotide sequences reported in this paper have been submitted to GenBank™ Data Base with the corresponding accession numbers: DQ466890; AY844960; AY789449-453; AY844959.
References
- 1 Luckner M, Wichtl M. In: Luckner M, Wichtl M, editors Digitalis. Stuttgart; WVGmbH 2000: 1-352.
- 2 Kreis W, Hensel A, Stuhlemmer U. Cardenolide biosynthesis in foxglove. Planta Med. 1998; 64 491-9.
- 3 Seidel S, Kreis W, Reinhard E. Δ5-3β-Hydroysteroid dehydrogenase/Δ5-Δ4-ketosteroid isomerase (3β-HSD), a possible enzyme of cardiac glycoside biosynthesis, in cell cultures and plants of Digitalis lanata EHRH. Plant Cell Rep. 1990; 8 621-4.
- 4 Finsterbusch A, Lindemann P, Grimm R, Eckerskorn C, Luckner M. Δ5-3β-Hydroxysteroid dehydrogenase from Digitalis lanata Ehrh - a multifunctional enzyme in steroid metabolism?. Planta. 1999; 209 479-86.
-
5 Lindemann P, Finsterbusch A, Pangert A, Luckner M. Partial cloning of a Δ5 - 3β-hydroxysteroid dehydrogenase from Digitalis lanata
. In: Okamoto M, Ishimura Y, Nawata, H, editors
Molecular steroidogenesis, Proceedings of the Yamada Conference LII . Tokyo; Universal Academy Press, Frontiers Science Series 29 - XXIV 2000: 333-4. - 6 Simard J, Ricketts M -L, Gingras S, Soucy P, Feltus F A, Melner M H. Molecular biology of the 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 isomerase gene family. Endocrine Rev. 2005; 26 525-82.
- 7 Persson B, Krook M, Jörnvall H. Characteristics of short-chain alcohol dehydrogenases and related enzymes. Eur J Biochem. 1991; 200 537-43.
- 8 Djerassi C, Engle R R, Bowers A. The direct conversion of steroidal Δ5-3β-alcohols to Δ5- and Δ4-3-ketones. J Org Chem. 1956; 21 547-9.
- 9 Kreis W, Zhu W, Reinhard E. 12β-hydroxylation of digitoxin by Digitalis lanata cells. Production of deacetyllanatoside C in a 20-L airlift bioreactor. Biotechnol Lett. 1989; 11 25-30.
- 10 Kreis W, Reinhard E. 12β-hydroxylation of digitoxin by suspension-cultured Digitalis lanata cells. Production of deacetyllanatoside C using a two-stage culture method. Planta Med. 1988; 54 95-100.
- 11 Sambrook J, Fritsch E F, Maniatis T. Molecular Cloning. A laboratory manual, 2nd edition. New York; Cold Spring Harbor Press 1989.
- 12 Williams B, Tsang A. A maize gene expressed during embryogenesis is ABA-inducible and highly conserved. Plant Mol Biol. 1991; 16 919-23.
- 13 Müller-Uri F, Reva V A. Overexpression and catalytic function of cyclophilin 18 from Digitalis lanata Ehrh. Pharm Pharmacol Lett. 2000; 10 5-7.
- 14 Herl V, Fischer G, Müller-Uri F, Kreis W. Molecular cloning and heterologous expression of progesterone 5β-reductase from Digitalis lanata Ehrh. Phytochemistry. 2006; 67 25-31.
- 15 Bradford M M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976; 72 248-54.
- 16 Jork H. Thin Layer Chromatography: Reagents and Detection Methods, Vol. 1. In: Jork H., Funk W, Fischer W, editors. Thin-Layer-Chromatography. New York: VCH. Publishers; 2004 195-8.
- 17 Ringer K L, Davis E M, Croteau R. Monoterpene metabolism. Cloning, expression, and characterization of (-)-isopiperitenol/(-)-carveol dehydrogenase of peppermint and spearmint. Plant Physiol. 2005; 137 863-72.
- 18 Xia Z -Q, Costa M A, Pélissier H C, Davin L B, Lewis N G. Secoisolariciresinol dehydrogenase purification, cloning, and functional expression. J Biol Chem. 2001; 276 12 614-23.
- 19 Jörnvall H, Persson B, Krook M, Atrian S, Gonzalez-Duarte R, Jeffery J. et al . Short-chain dehydrogenases/reductases (SDR). Biochemistry. 1995; 34 6003-13.
- 20 Jez J M, Bennett M J, Schlegel B P, Lewis M, Penning T M. Comparative anatomy of the aldo-keto reductase superfamily. Biochem J. 1997; 326 625-36.
- 21 Oppermann U CT, Maser E. Characterization of a 3α-hydroxysteroid dehydrogenase/carbonyl reductase from the gram-negative bacterium Commamonas testosteroni . Eur J Biochem. 1996; 209 459-66.
- 22 Oppermann U CT, Filling C, Berndt K D, Persson B, Benach J, Ladenstein R. et al . Active site directed mutagenesis of 3β/17β-hydroxysteroid dehydrogenase establishes differential effects on short-chain dehydrogenase/reductase reactions. Biochemistry. 1997; 36 34-40.
- 23 Thomas J L, Berko E A, Faustino A, Myers R P, Strickler R C. Human placental 3β-hydroxy-5-ene-steroid dehydrogenase and steroid 5-4-ene-isomerase: purification from microsomes, substrate kinetics, and inhibition by product steroids. J Steroid Biochem. 1988; 31 785-93.
- 24 Benach J, Filling C, Oppermann U C, Roversi P, Bricogne G, Berndt K D. et al . Structure of bacterial 3β/17β-hydroxysteroid dehydrogenase at 1.2 A resolution: a model for multiple steroid recognition. Biochemistry. 2002; 41 4659-68.
- 25 Stuhlemmer U, Kreis W. Cardenolide formation and activity of pregnane-modifying enzymes in cell suspension cultures, shoot cultures and leaves of Digitalis lanata . Plant Physiol Biochem. 1996; 34 85-91
- 26 Seitz H U, Gärtner D E. Enzymes is cardenolide-accumulating shoot cultures of Digitalis purpurea L. Plant Cell Tissue Organ Cult. 1994; 38 337-44.
- 27 Pollack R M. Enzymatic mechanisms for catalysis of enolization: ketosteroid isomerase. Bioorg Chem. 2004; 32 341-53.
- 28 Houck W J, Pollack R M. Activation enthalpies and entropies for the microscopic rate constants of acetate-catalyzed isomerization of 5-androstene-3,17-dione. J Am Chem Soc. 2003; 125 10 206-12.
- 29 Krozowski Z. The short-chain alcohol dehydrogenase superfamily: variations on a common theme. J. Steroid Biochem Mol Biol. 1994; 51 125-30.
1 The nucleotide sequences reported in this paper have been submitted to GenBank™ Data Base with the corresponding accession numbers: DQ466890; AY844960; AY789449-453; AY844959.
Prof. Dr. Wolfgang Kreis
Lehrstuhl Pharmazeutische Biologie
Friedrich-Alexander-Universität Erlangen-Nürnberg
Staudtstr. 5
91058 Erlangen
Germany
Telefon: +49-9131-852-8241
Fax: +49-9131-852-8243
eMail: wkreis@biologie.uni-erlangen.de
- www.thieme-connect.de/ejournals/toc/plantamedica