Abstract
A full-length cDNA clone that encodes progesterone 5β-reductase (5β-POR, EC 1.3.1.3)
was isolated from Isoplexis canariensis leaves. The reading frame of the Ic5β-POR gene is 1170 nucleotides corresponding to 389 amino acids. The SphI/SalI Ic5β-POR fragment was cloned into the pQE vector system and then transformed into Escherichia coli strain M15[pREP4]. The gene was functionally expressed and the recombinant enzyme
was characterised. K
m and V
max were calculated to be 0.215 mM and 46.4 nkat/mg protein, respectively, using progesterone
as the substrate. Kinetic constants for cortisol, cortexone, 4-androstene-3,17-dione
and NADPH were also determined. The 5β-POR from I. canariensis shows a significant homology to the putative progesterone 5β-reductases isolated
from other plant species, such as Digitalis lanata and Arabidopsis thaliana.
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F. Müller-Uri
Lehrstuhl für Pharmazeutische Biologie
Friedrich-Alexander-Universität Erlangen-Nürnberg
Staudtstr. 5
91058 Erlangen
Germany
Phone: +49-9131-852-8251
Email: fmueller@biologie.uni-erlangen.de