Alkaloids from Vinca minor L. XXI. The structure of vincaminoridine and vincoridine

1968 ◽  
Vol 33 (12) ◽  
pp. 4328-4336 ◽  
Author(s):  
I. Kompiš ◽  
J. Mokrý
Keyword(s):  
Plant Science ◽  
1988 ◽  
Vol 54 (1) ◽  
pp. 83-91 ◽  
Author(s):  
O.C. Elavummoottil ◽  
S. Duret ◽  
A. Vannereau ◽  
L. Cosson ◽  
J.C. Mestre
Keyword(s):  

2011 ◽  
Vol 107 (9) ◽  
pp. 1445-1452 ◽  
Author(s):  
Yong-Qiang Wang ◽  
Rainer Melzer ◽  
Günter Theißen
Keyword(s):  

1988 ◽  
pp. 271-274
Author(s):  
M. Caruso ◽  
L. Crespi-Perellino ◽  
L. Garofano ◽  
A. Guicciardi

2019 ◽  
Vol 168 ◽  
pp. 112110 ◽  
Author(s):  
Sara Abouzeid ◽  
Tahani Hijazin ◽  
Laura Lewerenz ◽  
Robert Hänsch ◽  
Dirk Selmar

2015 ◽  
Vol 51 (5) ◽  
pp. 572-578 ◽  
Author(s):  
S. M. Grujić ◽  
I. D. Radojević ◽  
S. M. Vasić ◽  
L. R. Čomić ◽  
M. D. Topuzović

2012 ◽  
Vol 111 (2) ◽  
pp. 239-245 ◽  
Author(s):  
Priyanka Verma ◽  
Ajay K. Mathur ◽  
Karuna Shanker
Keyword(s):  

Biomolecules ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1595
Author(s):  
Emily Amor Stander ◽  
Liuda Johana Sepúlveda ◽  
Thomas Dugé de Bernonville ◽  
Inês Carqueijeiro ◽  
Konstantinos Koudounas ◽  
...  

The lesser periwinkle Vinca minor accumulates numerous monoterpene indole alkaloids (MIAs) including the vasodilator vincamine. While the biosynthetic pathway of MIAs has been largely elucidated in other Apocynaceae such as Catharanthus roseus, the counterpart in V. minor remains mostly unknown, especially for reactions leading to MIAs specific to this plant. As a consequence, we generated a comprehensive V. minor transcriptome elaborated from eight distinct samples including roots, old and young leaves exposed to low or high light exposure conditions. This optimized resource exhibits an improved completeness compared to already published ones. Through homology-based searches using C. roseus genes as bait, we predicted candidate genes for all common steps of the MIA pathway as illustrated by the cloning of a tabersonine/vincadifformine 16-O-methyltransferase (Vm16OMT) isoform. The functional validation of this enzyme revealed its capacity of methylating 16-hydroxylated derivatives of tabersonine, vincadifformine and lochnericine with a Km 0.94 ± 0.06 µM for 16-hydroxytabersonine. Furthermore, by combining expression of fusions with yellow fluorescent proteins and interaction assays, we established that Vm16OMT is located in the cytosol and forms homodimers. Finally, a gene co-expression network was performed to identify candidate genes of the missing V. minor biosynthetic steps to guide MIA pathway elucidation.


2015 ◽  
Vol 3 (5) ◽  
pp. 1500015
Author(s):  
Sina Moeller ◽  
Tina Wöhrmann ◽  
Bruno Huettel ◽  
Kurt Weising

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