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The influence of salicylic acid elicitation of shoots, callus, and cell suspension cultures on production of naphtodianthrones and phenylpropanoids in Hypericum perforatum L.

Authors :
Gadzovska, Sonia
Maury, Stéphane
Delaunay, Alain
Spasenoski, Mirko
Hagège, Daniel
Courtois, Didier
Joseph, Claude
Source :
Plant Cell, Tissue & Organ Culture; Apr2013, Vol. 113 Issue 1, p25-39, 15p
Publication Year :
2013

Abstract

Hypericum perforatum is a well known medicinal plant. The main pharmacological properties are due to the presence of naphtodianthrones such as hypericin and pseudohypericin. Unfortunately the levels of these compounds vary under different environmental conditions. Elicitation of in vitro cultures is a useful approach to enhance and extend production of desirable products. Therefore, the effects of salicylic acid were characterized on different explants of H. perforatum L. (cells, calli and shoots) cultured in vitro. It appears at first that salicylic acid did not affect growth and development of these explants. In addition, the production of both hypericin and pseudohypericin has doubled in elicited cell suspension cultures but not in the two other cultures. Furthermore, phenylpropanoids that are among the most frequently observed metabolites affected upon treatment of in vitro culture material with elicitors, were produced and the enzymatic activities of phenylalanine ammonia lyase and of chalcone isomerase were stimulated upon elicitation. These effects were dependant of the type of in vitro culture, the concentration of salicylic acid and the duration post-elicitation. The H. perforatum cells were globally more sensitive to salicylic acid elicitation when maintained in an undifferentiated state and particularly in cell suspension cultures. In the absence of glands considered as the sites of naphtodianthrones biosynthesis, cells and calli were capable of producing these compounds. This implies that salicylic acid could act at biosynthesis level but not for the accumulation of both hypericin and pseudohypericin. Consequently, the regulation of this process is more complex than cited in the literature involving the responsibility of only Hyp- 1 gene, encoding a hypericin biosynthetic enzyme, cloned and characterized from H. perforatum. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01676857
Volume :
113
Issue :
1
Database :
Complementary Index
Journal :
Plant Cell, Tissue & Organ Culture
Publication Type :
Academic Journal
Accession number :
86304942
Full Text :
https://doi.org/10.1007/s11240-012-0248-0