Comparison of Various Strategies Designed to Optimize Indole Alkaloid Accumulation of a Cell Suspension Culture of Catharanthus roseus

1987 ◽  
Vol 42 (9-10) ◽  
pp. 1101-1108 ◽  
Author(s):  
Jochen Berlin ◽  
Christiane Mollenschott ◽  
Frank DiCosmo

The cell line CP-3 of Catharanthus roseus produces low levels of indole alkaloids during station­ary phase of growth, but increased levels when transferred to growth-limiting production media. Highest specific yields of alkaloids were usually achieved 8-15 days after transfer of the cells to the production medium. We attempted to reduce the time required for alkaloid production by altering preculture conditions, and by adding an elicitor preparation known to stimulate alkaloid accumulation in other cells. Reduction of 2,4-D in the last growth medium before transfer to production medium and a high initial inoculum load into the production medium resulted in rapid and greatest alkaloid accumulation (up to 2 mg ajmalicine/g dry mass or 40 mg/1 within 7 days). The addition of elicitor to the cell suspension stimulated high levels of tryptamine biosynthesis and accumulation under all culture conditions. Additionally, two cell lines derived from CP-3 cells and maintained on NAA/kinetin containing medium were selected for rapid growth in the absence of 2,4-D and were characterized with respect to their ajmalicine production. At a high inoculum load these cells produced up to 1.3 mg/g or 20 mg ajmalicine/1 when cultivated on the growth medium. The biotechnological utility of such cell lines is discussed.

1987 ◽  
Vol 42 (9-10) ◽  
pp. 1075-1081 ◽  
Author(s):  
Otmar Schiel ◽  
Ludger Witte ◽  
Jochen Berlin

The activity of geraniol- 10-hydroxylase was greatly increased when Catharanthus roseus cells were transferred to a production medium for monoterpene indole alkaloids. Its activity pattern showed a closer relationship than tryptophan decarboxylase to the pattern of indole alkaloid accumulation. The intermediate accumulation of tryptamine and its later incorporation into ajmalicine indicated that the coordination of the two precursor pathways for the monoterpene indole alkaloid formation was not synchronized under the chosen culture conditions. A better tuning of these two pathways may shorten the time period for induction of indole alkaloid biosynthesis.


1985 ◽  
Vol 40 (1-2) ◽  
pp. 21-25 ◽  
Author(s):  
H.-A. Arfmann ◽  
W. Kohl ◽  
V. Wray

A cell suspension culture of Catharanthus roseus was treated during the growth phase with the nucleoside analogue 5-azacytidine, a powerful inducer of cell differentiation, as evidenced with animal and human cell lines. After induction the cell culture was further incubated in a production medium in the absence of the inducer for 10 days. The extraction of the freeze dried cells and analysis by high performance liquid chromatography showed an additional intense peak in the elution profile, not present in extracts of untreated cells. The structure of the newly synthesized metabolite, elucidated by mass spectrometry and 1H and 13C NMR, was a lignan type compound, lirioresinol B mono-β-D-glucoside. This compound has hitherto not been found in Catharanthus roseus plants or cell cultures.


Plants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 672
Author(s):  
Tran My Linh ◽  
Nguyen Chi Mai ◽  
Pham Thi Hoe ◽  
Ninh Thi Ngoc ◽  
Phan Thi Hong Thao ◽  
...  

Cell and tissue cultures of Catharanthus roseus have been studied extensively as an alternative strategy to improve the production of valuable secondary metabolites. The purpose of this study was to produce C. roseus callus and suspension cell biomass of good quality and quantity to improve the total alkaloids and bis-indole alkaloids. The young stem derived-callus of C. roseus variety Quang Ninh (QN) was grown on MS medium supplemented with 1.5 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) plus 1.5 mg/L kinetin, and the growth rate increased by 67-fold after 20 days. The optimal conditions for maintaining the cell suspension culture were 150 mg/50 mL cell inoculum, a medium pH of 5.5 and a culture temperature of 25 °C. The low alkaloid content in the culture was compensated for by using endophytic fungi isolated from local C. roseus. Cell extracts of endophytic fungi—identified as Fusarium solani RN1 and Chaetomium funicola RN3—were found to significantly promote alkaloid accumulation. This elicitation also stimulated the accumulation of a tested bis-indole alkaloid, vinblastine. The findings are important for investigating the effects of fungal elicitors on the biosynthesis of vinblastine and vincristine, as well as other terpenoid indole alkaloids (TIAs), in C. roseus QN cell suspension cultures.


1981 ◽  
Vol 36 (1-2) ◽  
pp. 40-43 ◽  
Author(s):  
K.-H. Knobloch ◽  
B. Hansen ◽  
J. Berlin

Abstract Recently medium conditions have been developed which stimulate the formation of the indole alkaloid ajmalicine in cell suspension cultures of Catharanthus roseus [6]. When cells were subjected to these conditions the alkaloid accumulation was preceded by a 12-fold increase of the specific activity of tryptophan decarboxylase. The enzyme activity showed a maximum two days after the cell transfer into the induction medium and subsequently declined. In contrast the activity of strictosidine synthase, the enzyme condensing tryptamine and secologanin, was present over the entire measuring period at a constant level. The intracellular content of tryp­tamine and ajmalicine increased during a period of 6 days after cell transfer and reached a plateau after that time. A possible regulatory function of tryptophan decarboxylase in indole alkaloid biosynthesis is discussed.


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