Plant Physiol, April 2000, Vol. 122, pp. 1261-1268
Phytoene Desaturase Is Localized Exclusively in the Chloroplast
and Up-Regulated at the mRNA Level during Accumulation of Secondary
Carotenoids in Haematococcus pluvialis (Volvocales,
Chlorophyceae)1,2
Kay
Grünewald,*
Manfred
Eckert,
Joseph
Hirschberg, and
Christoph
Hagen
Institute of General Botany, Friedrich-Schiller-University Jena, Am
Planetarium 1, D-07743 Jena, Germany (K.G., C.H.); Institute of
General Zoology, Friedrich-Schiller-University Jena, Erbertstrasse
1, D-07743 Jena, Germany (M.E.); and Department of Genetics, The
Hebrew University of Jerusalem, Jerusalem, 91904 Israel (J.H.)
The
unicellular green alga Haematococcus pluvialis Flotow is
known for its massive accumulation of ketocarotenoids under various stress conditions. Therefore, this microalga is one of the favored organisms for biotechnological production of these antioxidative compounds. Astaxanthin makes up the main part of the secondary carotenoids and is accumulated mostly in an esterified form in extraplastidic lipid vesicles. We have studied phytoene desaturase, an
early enzyme of the carotenoid biosynthetic pathway. The increase in
the phytoene desaturase protein levels that occurs following induction
is accompanied by a corresponding increase of its mRNA during the
accumulation period, indicating that phytoene desaturase is regulated
at the mRNA level. We also investigated the localization of the enzyme
by western-blot analysis of cell fractions and by immunogold labeling
of ultrathin sections for electron microscopy. In spite of the fact
that secondary carotenoids accumulate outside the chloroplast, no extra
pathway specific for secondary carotenoid biosynthesis in H.
pluvialis was found, at least at this early stage in the
biosynthesis. A transport process of carotenoids from the site of
biosynthesis (chloroplast) to the site of accumulation (cytoplasmatic
located lipid vesicles) is implicated.
1
This study was supported in part by the
Deutscher Akademischer Austauschdienst (short-term fellowship to K.G.),
by the Thüringer Ministerium für Forschung, Wissenschaft
und Kultur (grant no. B301-69013), and by a graduate fellowship from
the Freistaat Thüringen for K.G.
2
This paper is dedicated to the occasion of the
65th birthday of Prof. Dr. Wolfram Braune.
*
Corresponding author; e-mail kay.gruenewald{at}rz.uni-jena.de; fax
49-3641-949225.
© 2000 American Society of Plant Physiologists