Plant Physiol. Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 94:1323-1329 (1990)
© 1990 American Society of Plant Biologists

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by De Carolis, E.
Right arrow Articles by De Luca, V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by De Carolis, E.
Right arrow Articles by De Luca, V.
Agricola
Right arrow Articles by De Carolis, E.
Right arrow Articles by De Luca, V.
Metabolism and Enzymology

Isolation and Characterization of a 2-Oxoglutarate Dependent Dioxygenase Involved in the Second-to-Last Step in Vindoline Biosynthesis 1,2

Emidio De Carolis, Francis Chan2, John Balsevich and Vincenzo De Luca

Département de Sciences Biologique, Université de Montréal, Saskatoon, Saskatchewan Canada S7N 0W9, Plant Biotechnology Institute, National Research Council of Canada, Saskatoon, Saskatchewan Canada S7N 0W9

Young leaves from Catharanthus roseus plants contain the enzymes which convert the monoterpenoid indole alkaloid, tabersonine by three hydroxylations, two methylations, and one acetylation step to vindoline. A novel direct enzyme assay has been developed for a hydroxylase involved in vindoline biosynthesis, which catalyzes the C4-hydroxylation of 2,3-dihydro-3-hydroxy-N(1)-methyltabersonine to the 3,4-dihydroxy derivative. The enzyme showed an absolute requirement for 2-oxoglutarate and enzymatic activity was enhanced by ascorbate, establishing it as a 2-oxoglutarate-dependent dioxygenase (EC 1.14.11.-). The hydroxylase exhibited specificity for position 4 of various alkaloid substrates. The enzyme exhibited a pH optima between 7 and 8 and an apparent molecular weight of 45,000. The appearance of 4-hydroxylase activity was developmentally regulated and was shown to be inducible by light treatment of seedlings. Substrate specificity studies of this enzyme for indole alkaloid substrate suggested that hydroxylation at position 3 and N-methylation occur prior to hydroxylation at position 4. This is in agreement with previous studies which suggest that C4-hydroxylation is the second to last step in vindoline biosynthesis in Catharanthus roseus.


2 3 Present address: University of British Columbia Medical School, 156 Main Mall Vancouver, British Columbia Canada V6T 1W5. This is study NRCC No. 32452.

1 This work was supported by the National Research Council of Canada (NRCC) (F.C., J.B., and V.D.L.), Natural Sciences and Engineering Research Council of Canada (V.D.L.), and the Department of Higher Education, Government of Quebec (FCAR: V.D.L. and E.D.C.). E.D.C. was the recipient of a Faculte des Etudes Superieures scholarship.

2 Present address: University of British Columbia Medical School, 156 Main Mall Vancouver, British Columbia Canada V6T 1W5. This is study NRCC No. 32452.




This article has been cited by other articles:


Home page
Plant CellHome page
B. St-Pierre, F. A. Vazquez-Flota, and V. De Luca
Multicellular Compartmentation of Catharanthus roseus Alkaloid Biosynthesis Predicts Intercellular Translocation of a Pathway Intermediate
PLANT CELL, May 1, 1999; 11(5): 887 - 900.
[Abstract] [Full Text]


Home page
Plant Physiol.Home page
F. A. Vazquez-Flota and V. De Luca
Developmental and Light Regulation of Desacetoxyvindoline 4-Hydroxylase in Catharanthus roseus (L.) G. Don. . Evidence of a Multilevel Regulatory Mechanism
Plant Physiology, August 1, 1998; 117(4): 1351 - 1361.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY THE PLANT CELL
Copyright © 1990 by the American Society of Plant Biologists