Planta Med 2010; 76(9): 928-934
DOI: 10.1055/s-0030-1250036
Biochemistry, Molecular Biology and Biotechnology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Pinoresinol-Lariciresinol Reductases with Opposite Enantiospecificity Determine the Enantiomeric Composition of Lignans in the Different Organs of Linum usitatissimum L.[*]

Shiva Hemmati1 , 3 , Cosima B. I. von Heimendahl1 , Michael Klaes2 , A. Wilhelm Alfermann1 , Thomas J. Schmidt2 , Elisabeth Fuss1 , 4
  • 1Institut für Entwicklungs- und Molekularbiologie der Pflanzen, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany
  • 2Institut für Pharmazeutische Biologie und Phytochemie (IPBP), Westfälische Wilhelms-Universität Münster, Münster, Germany
  • 3Present address: Department of Biochemistry, Purdue University, West Lafayette, Indiana, USA
  • 4Present address: Interfakultäres Institut für Biochemie, Eberhard Karls Universität Tübingen, Tübingen, Germany
Further Information

Publication History

received March 25, 2010 revised May 7, 2010

accepted May 10, 2010

Publication Date:
31 May 2010 (online)

Abstract

Lignans in higher plants represent an ideal class of natural products to be investigated for the origin of stereochemical diversity since chiral lignans occur in pure enantiomeric form as well as in enantiomeric mixtures. Seeds of Linum usitatissimum contain 8S, 8′S-(+)- and 8R, 8′R-(−)-secoisolariciresinol [SS-(+)- and RR-(−)-secoisolariciresinol, respectively] as diglucosides (SS- and RR-secoisolariciresinol diglucosides) whereas aerial parts of flowering L. usitatissimum accumulate only lignans derived from RR-(−)-secoisolariciresinol. Pinoresinol-lariciresinol reductase (PLR) catalyzes two early steps in lignan biosynthesis. Up to now, only a cDNA encoding a PLR (PLR‐Lu1) which is enantiospecific for the conversion of 8S, 8′S-(−)-pinoresinol (SS-pinoresinol) via 8S, 8′S-(−)-lariciresinol (SS-lariciresinol) to SS-(+)-secoisolariciresinol was cloned. Here we present the cloning of a cDNA encoding a RR-pinoresinol-RR-lariciresinol reductase (PLR‐Lu2) from the leaves of L. usitatissimum which converts only RR-pinoresinol to RR-secoisolariciresinol. In leaves and stems of L. usitatissimum accumulating the 8R, 8′R-enantiomers of lignans, only PLR‐Lu2 was transcriptionally active. Both PLR‐Lu1 and PLR‐Lu2 transcripts were observed in seeds and contribute to the synthesis of SS- and RR-secoisolariciresinol, respectively. Thus, the enantiomeric composition of lignans in the organs of L. usitatissimum appears to be determined by the relative action of two PLRs with opposite enantiospecificities rather than by a single enzyme of low enantiospecificity.

1 Dedicated to Prof. Dr. Wolfgang Barz on the occasion of his 75th birthday.

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1 Dedicated to Prof. Dr. Wolfgang Barz on the occasion of his 75th birthday.

Elisabeth Fuss (Molecular biology)

Interfakultäres Institut für Biochemie
Universität Tübingen

Hoppe-Seyler-Str. 4

72076 Tübingen

Germany

Phone: +497 07 12 97 33 27

Fax: +49 70 71 29 50 70

Email: elisabeth.fuss@uni-tuebingen.de

Thomas J. Schmidt (Analytical phytochemistry)

Institut für Pharmazeutische Biologie und Phytochemie (IPBP)
Westfälische Wilhelms-Universität Münster

Hittorfstraße 56

48149 Münster

Germany

Phone: +49 25 18 33 33 78

Fax: +49 25 18 33 83 41

Email: thomschm@uni-muenster.de

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