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Dedicated Roles of Plastid Transketolases during the Early Onset
of Isoprenoid Biogenesis in Pepper Fruits1
Florence Bouvier,
Alain d'Harlingue,
Claude Suire,
Ralph A. Backhaus, and
Bilal Camara*
Institut de Biologie Moléculaire des Plantes du Centre
National de la Recherche Scientifique and Université Louis
Pasteur, 12 rue du Général Zimmer, 67084 Strasbourg, France
(F.B., B.C.); Laboratoire de Pathologie et Biochimie
Végétales, Université Pierre et Marie Curie, 4 Place
Jussieu, 75250 Paris, France (A.d.'H.); Laboratoire de Pathologie et Biochimie
Végétales, Université Pierre et Marie Curie, 4 Place
Jussieu, 75250 Paris, France (A.d.'H.)Institut de Biochimie et
Génétique Cellulaire du Centre National de la Recherche
Scientifique, 1 rue Camille Saint Saëns, 33077 Bordeaux, France
(C.S.); and Department of Botany, P.O. Box 871601, Arizona State
University, Tempe, Arizona 85287-1601 (R.A.B.)
Isopentenyl diphosphate (IPP), which
is produced from mevalonic acid or other nonmevalonic substrates, is
the universal precursor of isoprenoids in nature. Despite the presence
of several isoprenoid compounds in plastids, enzymes of the mevalonate
pathway leading to IPP formation have never been isolated or identified
to our knowledge. We now describe the characterization of two pepper (Capsicum annuum L.) cDNAs, CapTKT1 and CapTKT2, that
encode transketolases having distinct and dedicated specificities.
CapTKT1 is primarily involved in plastidial pentose phosphate and
glycolytic cycle integration, whereas CapTKT2 initiates the synthesis
of isoprenoids in plastids via the nonmevalonic acid pathway. From
pyruvate and glyceraldehyde-3-phosphate, CapTKT2 catalyzes the
formation of 1-deoxy-xylulose-5-phosphate, the IPP precursor. CapTKT1
is almost constitutively expressed during the
chloroplast-to-chromoplast transition, whereas CapTKT2 is overexpressed
during this period, probably to furnish the IPP necessary for increased
carotenoid biosynthesis. Because deoxy-xylulose phosphate is shared by
the plastid pathways of isoprenoid, thiamine (vitamin B1),
and pyridoxine (vitamin B6) biosynthesis, our results may
explain why albino phenotypes usually occur in thiamine-deficient
plants.
*
Corresponding author; e-mail camara{at}medoc.u-strasbg.fr; fax
33-38-86-14-442.
Plant Physiol. (1998) 117: 1423-1431
Copyright Clearance Center: 0032-0889/98/117//09
© 1998 American Society of Plant Physiologists
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