Effects of aluminium chloride on cell growth and production of coumarins in cell suspension cultures of Angelica archangelica L.


Vliv chloridu hlinitého na buněčný růst a produkci kumarinů v suspenzní kultuře Angelica archangelica L.

Elicitace rostlinných buněk v kultuře představuje užitečný biotechnologický nástroj pro zvýšení produkce sekundárních metabolitů. V této práci byl sledován vliv různých koncentrací chloridu hlinitého (1, 10, 50, 100, 500, 1000 μM) jako potenciálního elicitoru produkce kumarinů v suspenzní kultuře anděliky lékařské. Byla posuzována také toxicita hlinitých iontů pro kulturu hodnocením jejich účinku na buněčný růst (charakterizován čerstvou a suchou hmotností biomasy na konci čtrnáctidenní kultivace). Kultury byly kultivovány ve tmě a na světle. Čerstvá hmotnost nebyla chloridem hlinitým v koncentraci 1 až 1000 μM signifikantně ovlivněna. Suchá hmotnost byla snížena asi o 10 % při koncentraci chloridu hlinitého 1000 μM. Produkce kumarinů byla chloridem hlinitým ovlivněna v závislosti na světelných podmínkách. V kulturách kultivovaných ve tmě zvyšovaly hlinité ionty množství kumarinů v médiu od koncentrace 10 μM, v buňkách od koncentrace 50 μM. Obsah kumarinů rostl se zvyšující se hladinou hlinitých iontů. Nejlepší výsledky byly dosaženy s koncentrací 1000 μM chloridu hlinitého. Obsah kumarinů byl ve srovnání s kontrolní kulturou zvýšen o 33 % v médiu a o 24 % v buňkách. Naproti tomu v kulturách kultivovaných na světle chlorid hlinitý produkci kumarinů nezvýšil. Jeho vyšší koncentrace tvorbu kumarinů v těchto kulturách ještě snížily.

Klíčová slova:
Angelica archangelica L. – suspenzní kultura – růst – kumariny – hliník – elicitace – světelné podmínky – sekvenční injekční analýza


Authors: T. Siatka;  M. Kašparová
Authors place of work: Charles University in Prague, Faculty of Pharmacy in Hradec Králové, Department of Pharmacognosy
Published in the journal: Čes. slov. Farm., 2010; 59, 112-116
Category: Původní práce

Summary

Elicitation of plant cells in culture represents a useful biotechnological tool to improve the production of secondary metabolites. In this study, aluminium chloride at various concentrations (1, 10, 50, 100, 500, and 1000 μM) was tested as a potential elicitor of the production of coumarins in angelica cell suspension cultures. In addition, the toxicity of aluminium ions for the culture was assessed by evaluating their effect on cell growth (characterized by fresh and dry biomass at the end of a two-week subculture). Cultures were cultured in the dark or in the light. Fresh biomass was not affected significantly in the presence of aluminium chloride at concentrations from 1 to 1000 μM. Dry biomass was reduced by about 10% at an aluminium concentration of 1000 μM. Production of coumarins was influenced by aluminium chloride depending on light conditions. In the dark-grown cultures, aluminium ions from a concentration of 10 and 50 μM enhanced accumulation of coumarins in the medium and cells, respectively. The contents of coumarins rose with an increasing aluminium level. The best results were achieved with 1000 μM aluminium chloride. The amounts of coumarins were increased by 33% in the medium and 24% in the cells as compared with control cultures. On the other hand, production of coumarins was not improved by aluminium chloride in the light-grown cultures. Moreover, higher aluminium concentrations lowered formation of coumarins in these cultures.

Key words:
Angelica archangelica L. – cell suspension cultures – growth – coumarins – aluminium – elicitation – light conditions – sequential injection analysis

Introduction

Plant secondary metabolites are unique sources for pharmaceuticals, food additives, flavours, and other industrial materials. Plant cell culture technology has been developed as a promising alternative for producing metabolites that are difficult to be obtained by chemical synthesis or plant extraction. One of the major obstacles hindering its wider application is the low yield of plant secondary metabolites in plant cell cultures 1). Many approaches have been developed to overcome this problem 2, 3). Perhaps the most notable strategy for improving metabolite yields is elicitation 4).Elicitors are factors that can induce an up-regulation of genes. Some elicitors target secondary metabolic genes, which are often associated with defense responses to perceived environmental changes 1, 4). Elicitors may be biotic or abiotic. The biotic elicitors have biological origin (e.g. fungal homogenates, culture filtrates, and plant cell wall components). On the other hand, abiotic elicitors are not of a biological origin and are grouped in physical factors (such as thermal and osmotic stress, radiation, and wounding) and chemical compounds (e.g. heavy metal salts) 5). It is well known that treatment with elicitors causes an array of defence reactions, including the accumulation of secondary metabolites in intact plants 6–8) as well as in cell cultures 9–12).

We report here the effects of aluminium chloride as a potential elicitor on cell growth and production of coumarins in Angelica archangelica cell suspension cultures.

Material and methods

Chemicals

2,4-dichlorophenoxyacetic acid and 6-benzylaminopurine (Sigma, Praha, Czech Republic); scopoletin (Fluka, Praha, Czech Republic); aluminium chloride, sodium phosphate dibasic, and potassium phosphate monobasic (Lachema, Brno, Czech Republic).

Instruments

A PS 20A autoclave (Chirana, Brno, Czech Republic); a roller (Vývojové dílny, Academy of Sciences of the Czech Republic, Praha, Czech Republic); a 200S analytical scale (Sartorius, Göttingen, Germany); a laboratory centrifuge MPW 342 (MPW Med. instruments, Warsaw, Poland); a laboratory shaker KS 501 (IKA Labortechnik, Staufen, Germany); a peristaltic pump (Alitea Instruments, Seattle, U.S.A); an eight position selection valve (Vici Valco Instruments, Brockville, Canada); and a FS 970 fluorescence detector (Schoeffel Instrument Corp., Westwood, U.S.A.).

Cell suspension cultures and culture conditions

Cell suspension cultures of Angelica archangelica were established as described previously 13) and grown in liquid Murashige and Skoog medium 14) supplemented with 2 mg l-1 2,4-dichlorophenoxyacetic acid, 0.4 mg l-1 benzylaminopurine, and 30 g l-1 sucrose. The pH of all media was adjusted to 5.7 before autoclaving. The cultures were agitated in 250 ml flasks containing 30 ml of the medium on a roller apparatus at 8 rpm, incubated at 25°C under a 16/8 light/dark photoperiod or in the dark, and subcultured every 14 days.

For testing the effects of aluminium chloride, the cultures were cultured in Murashige and Skoog media supplemented with an appropriate concentration of aluminium chloride (1, 10, 50, 100, 500, and 1000 μM). Control cultures were cultured in a medium without the addition of aluminium chloride. After 14 days, the cultures were harvested, and the cell growth and production of coumarins were evaluated.

All experiments were carried out in triplicate and were repeated at least twice. Student’s t-test was used for statistical analysis of data, and differences with P < 0.05 were considered as statistically significant.

Analytical procedures

Cells were separated from the culture medium by vacuum filtration using a Buchner funnel with filter paper. For evaluation of the culture growth, filtered cells were washed with distilled water, weighed for fresh weight determination, and then dried to obtain dry weight.

Coumarins in cells and in the culture medium were quantified fluorometrically by sequential injection analysis (SIA) 15). The powdered dry cells were extracted three times (always for 15 min) with a mixture of equal volumes of methanol and 0.066 M phosphate buffer (pH 6) by shaking at 150 rpm on an orbital shaker at laboratory temperature. The extracts were pooled, adjusted to 25 ml with the extraction mixture, centrifuged at 3,000 rpm for 10 min, and analysed. The culture media were analysed directly. The SIA conditions were as follows – a carrier stream: water; flow rate: 3 ml/min; sample volume: 40 μl; volume of 0.066 M phosphate buffer (pH 6): 100 μl; a 1.5 ml mixing coil; excitation wavelength: 345 nm; and emission wavelength: cut-off emission filter transparent at ≥ 390 nm. The contents of coumarins were expressed as scopoletin (mg l-1 in the medium and mg g-1 dry weight in the cells).

Results and discussion

Aluminium is not regarded as an essential nutrient in plants. Aluminium is phytotoxic, particularly at pH values below 5.0, but its low concentrations can sometimes increase plant growth or induce other desirable effects. Plant species and varieties vary widely in tolerance to aluminium 16). Plants may adapt to higher levels of aluminium ions by various mechanisms. For example, aluminium can induce or stimulate biosynthesis of organic acids (such as citrate, malate and oxalate) 17, 18), callose 19) and pectin 20) formation, and synthesis of flavonoid type phenolics 18, 21, 22) and anthraquinones 23).

Aluminium ions in a wide range of concentrations were tested as a potential elicitor of production of coumarins in angelica cell suspension cultures. In addition, the toxicity of aluminium for the culture was assessed by evaluating its effect on cell growth, which was characterized by fresh and dry biomass at the end of a two-week subculture. Cultures were cultured in the dark or in the light because light conditions may influence both the growth and secondary metabolite formation in plant tissue cultures 24, 25).

As for culture growth (Table 1), fresh biomass was not influenced significantly in the presence of aluminium chloride at concentrations from 1 to 1000 μM. Dry biomass was not affected up to concentrations of 500 μM. Aluminium ions at 1000 μM reduced dry cell weight by about 12%, and by 9% in the dark-grown and light-grown cultures, respectively, in comparison with control cultures. An aluminium concentration of 5000 μM was lethal for angelica cell culture (data not shown).

Production of coumarins was influenced by aluminium chloride in dependence on light conditions (Fig. 1 and 2). Aluminium ions from a concentration of 10 and 50 μM enhanced accumulation of coumarins in the medium and cells, respectively, in the dark-grown cultures. The contents of coumarins rose with an increasing aluminium level. The best results were achieved with 1000 μM aluminium chloride. The amounts of coumarins were increased by 33% in the medium and 24% in the cells as compared with control cultures. On the other hand, production of coumarins was not improved by aluminium chloride in the light--grown cultures. Moreover, formation of coumarins declined in angelica cell cultures cultured in the light at higher aluminium concentrations.

Stimulating effects of aluminium ions have been reported on the production of flavanols in Vitis vinifera callus cultures 26) and diterpenoids in Jatropha elliptica root cultures 27). Similar findings regarding different response of a plant tissue culture to metal ions in dependence on light conditions have been observed, for instance, in cell suspension cultures of Angelica archangelica 28) and Digitalis lanata29).

This work was supported by the grants MSM 0021620822 and SVV-2010-261-002.

Address for correspondence:

PharmDr. Tomáš Siatka, CSc.
Charles University in Prague, Faculty of Pharmacy in Hradec Králové, Department of Pharmacognosy
Heyrovského 1203, 500 05 Hradec Králové
e-mail: siatka@faf.cuni.cz


Zdroje

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Štítky
Farmacie Farmakologie

Článek vyšel v časopise

Česká a slovenská farmacie

Číslo 3

2010 Číslo 3

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