THE EFFECT OF ARSENICALS ON ALKALOID PRODUCTION BY CELL-SUSPENSION CULTURES OF CATHARANTHUS-ROSEUS

Citation
Wr. Cullen et Di. Hettipathirana, THE EFFECT OF ARSENICALS ON ALKALOID PRODUCTION BY CELL-SUSPENSION CULTURES OF CATHARANTHUS-ROSEUS, Applied organometallic chemistry, 7(7), 1993, pp. 477-486
Citations number
24
Categorie Soggetti
Chemistry Applied","Chemistry Inorganic & Nuclear
ISSN journal
02682605
Volume
7
Issue
7
Year of publication
1993
Pages
477 - 486
Database
ISI
SICI code
0268-2605(1993)7:7<477:TEOAOA>2.0.ZU;2-X
Abstract
The effect of arsenic compounds on indole alkaloid production by cell suspension cultures of Catharanthus roseus was investigated. The analy sis of indole alkaloids was achieved by using thermospray liquid chrom atography-mass spectrometry (LC MS) which facilitated the rapid screen ing of alkaloid composition in cultures treated with different arsenic als at different times in their growth cycle. Treatment with dimethyla rsinate (DMA), a non-selective herbicide, has a drastic inhibitory eff ect on alkaloid production although it is the least toxic arsenical to growth. Tryptamine, an early precursor in the biosynthesis of indole alkaloids, accumulates in cells treated with DMA, indicating that the initial step of condensation of tryptamine with secologanin is inhibit ed. Treatment with DMA during the early stationary phase of culture gr owth enhances the accumulation of some alkaloids, although some, such as catharanthine, are suppressed. The arsenicals arsenate and methylar sonate (MMA) have an inhibitory effect on alkaloid production when app lied during the early growth stages. In contrast to MMA and DMA, arsen ate has a stimulatory effect on catharanthine production when introduc ed to the culture during its early stationary phase. Thus the changes in the pattern of alkaloid accumulation on addition of arsenicals are dependent on the arsenic species and its concentration, as well as the time of application. This variable response indicates that each arsen ical has a distinct mode of action on the secondary metabolic pathways of C. roseus.