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Plant Physiol, January 2001, Vol. 125, pp. 189-198
Molecular and Biochemical Analysis of a Madagascar Periwinkle
Root-Specific
Minovincinine-19-Hydroxy-O-Acetyltransferase1
Pierre
Laflamme,
Benoit
St-Pierre,2 and
Vincenzo
De Luca3*
Institut de Recherche en Biologie Végétale,
Département de Sciences Biologiques, Université de
Montréal, 4101 rue Sherbrooke est, Montreal, Quebec, Canada H1X
2B2
The terminal steps in the biosynthesis of the monoterpenoid indole
alkaloids vindoline and minovincinine are catalyzed by separate acetyl
coenzyme A-dependent O-acetyltransferases in Madagascar periwinkle (Catharanthus roseus G. Don). Two genes were
isolated that had 63% nucleic acid identity and whose deduced amino
acid sequences were 78% identical. Active enzymes that were expressed as recombinant His-tagged proteins in Escherichia coli
were named minovincinine-19-O-acetyltransferase (MAT)
and deacetylvindoline-4-O-acetyltransferase (DAT)
because they catalyzed the 19-O-acetylation of indole
alkaloids such as minovincinine and hörhammericine and the
4-O-acetylation of deacetylvindoline, respectively.
Kinetic studies showed that the catalytic efficiency of recombinant MAT
(rMAT) was very poor compared with that of recombinant DAT (rDAT),
whose turnover rates for Acetyl-coenzyme A and deacetylvindoline were
approximately 240- and 10,000-fold greater than those of rMAT.
Northern-blot analyses showed that MAT is expressed in cortical cells
of the root tip, whereas DAT is only expressed in specialized idioblast and laticifer cells within light exposed tissues like leaves and stems.
The coincident expression of trytophan decarboxylase, strictosidine synthase, and MAT within root cortical cells suggests that the entire
pathway for the biosynthesis of tabersonine and its substituted analogs
occurs within these cells. The ability of MAT to catalyze the
4-O-acetylation of deacetylvindoline with low efficiency
suggests that this enzyme, rather than DAT, is involved in vindoline
biosynthesis within transformed cell and root cultures, which
accumulate low levels of this alkaloid under certain circumstances.
1
This work was supported by a grant from the
National Sciences and Engineering Research Council of Canada (to
V.D.L.). P.L. was a recipient of a graduate studies scholarship
(Bourses Spéciales de la Faculté des Études
Supérieurs) from l'Université de Montréal.
2
Present address: Laboratoire de Physiologie
Végétale, EA 2106, Unité de Formation et de
Recherche des Sciences et Techniques, Université de Tours,
Parc de Grandmont, 37200 Tours, France.
3
Present address: Novartis Agribusiness
Biotechnology Research Inc., 3054 Cornwallis Road, Research Triangle
Park, NC, 27709-2257.
*
Corresponding author; e-mail
vince.deluca{at}nabri.Novartis.com; fax 919-541-8585.
© 2001 American Society of Plant Physiologists
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