Print version ISSN 0370-5943
Rev. latinoam. quím vol.38 no.2 Naucalpan de Juárez Aug. 2010
Phytotoxicity of indole alkaloids from cereals
Héctor R. Bravoª*, María José Iglesiasª, Sylvia V. Copajaª and Victor H. Argandoñab
ª Departamento de Química, Facultad de Ciencias, Universidad de Chile. Casilla 653, Santiago, Chile, Fax: 2713888, *Email: firstname.lastname@example.org
b Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Casilla 653, Santiago, Chile.
Received January 2010.
Accepted August 2010.
A test with the microalga Chlorella vulgaris was used to evaluate the allelopathic potential activity of indole alkaloids present in cereals. Gramine, the main indole alkaloid present in barley shows the highest toxicity. A model mechanism of action for auxin was used to analyze the structural effect on the observed toxicity.
Germination inhibition on seeds and shoot length inhibition activities of gramine on barley, rye, oat, wheat, lettuce cultivars and the weed Lollium rigidum were measured. Results are discussed in relation to the phytotoxic selectivity of gramine on the seeds germination. In addition, the toxicity of barley aqueous extracts on the germination of oat seed was also determined. Phytotoxicity of the extracts is in agreement with the phytotoxicity of pure gramine.
Key words: indole alkaloids, allelopathy, phytoactivity.
El potencial alelopático de alcaloides indólicos presentes en ciertas especies de cereales fue evaluado contra la microalga Chlorella vulgaris. Gramina, el principal alcaloide indólico presente en cebada mostró la mayor actividad. Un modelo mecanístico de acción para auxinas fue utilizado para analizar el efecto estructural en la toxicidad observada.
Se midió la inhibición de la germinación de semillas y el desarrollo de plántulas de cebada, centeno, avena, trigo, lechuga y la maleza Lollium rigidum por la acción de Gramina.
Los resultados son discutidos en relación a la fitotoxicidad selectiva de Gramina en la germinación de semillas. Además, se determinó la toxicidad de extractos de cebada en la germinación de semillas de avena. La fitotoxicidad de los extractos está de acuerdo con la fitotoxicidad de la Gramina pura.
Palabras claves: alcaloides indólicos, alelopatía, fitotoxicidad.
Secondary metabolites with toxic properties are thought to protect plants against pest and pathogens. In cereals of great agricultural importance, hydroxamic acids derived from 1,4benzoxazin3one (6) (Fig. 1) present in maize, wheat and rye, have been suggested to protect the plants against bacteria, fungi and insects (Sicker et al,. 2000; Sicker and Schulz, 2002; Copaja et al., 2006; Bravo et al., 2004). Indole Alkaloids such as 3N,Ndimethylaminomethyl indole (gramine) (1), Tryptamine (2), 5methoxytryptamine (3), 5methoxyN,Ndimethyl tryptamine (4), and NWmethyltryptamine (5) (Fig. 1) are present in various species of gramineae, leguminosae and other plant families (Miyagawa et al., 1994; Corcuera, 1993; Argandoña, 1987). They cause various deleterious effects on mammals, insects, fungi and bacteria (Corcuera, 1984; Matsuo et al,. 2001; Arnold and Hill, 1972; Pastuszewska et al,. 2001; Ishikawa and Kanke, 2000), which suggests a general role of these compounds against herbivores, pest and pathogens.
Other beneficial role of the secondary metabolites for the plants themselves arises from the phytotoxicity against competitive plants. Allelopathic interactions between individuals of different plant species or those of the same species are caused by plantproduced allelochemicals. Once released into the environment, they can influence germination, growth and development of neighboring plants either negatively or positively (Torres et al., 1996). Research in allelopathic interactions have been focused between agricultural crops and weeds, as an option on the development of integrated weed management strategies, reducing environmental effect and cost of crop protection (Batisch et al., 2001). For instance, allelopathic activity of decomposing straw of wheat and oat on some crop species has been reported (Dias, 1991). Allelopathic potential of rye (Putnam and De Frank, 1983; Sicker et al., 2000; Burgos and Talbert, 2000) and rice (Chou, 1980; Ahn and Chung, 2000) has been extensively studied. Allelochemicals such as phenolic acids, coumarines, hydroxamic acids and alkaloids have been reported to exist in these cereals.
Barley (Hordeum vulgare L.) is a smother crop, which can suppress the growth of weeds by competition with environmental resources (Overland, 1966). Competitiveness may arise from different allelochemicals present in barley (Baghestani et al., 1999).
Allelopathic potential of natural occurring indole alkaloids is not completely known. Therefore, to gain a deeper understanding of the phytotoxicity of these metabolites, we report in this work the antialgal activity of indole alkaloids against the alga Chlorella vulgaris, one of the most common used species in microalga toxicity test (Rioboo et al. 2002). Phytotoxicity of gramine was measured on the germination and shoot growth of a weed and competitive crop seeds. In addition, phytotoxicity of aqueous extracts of barley on oat seeds was evaluated.
MATERIAL AND METHODS
Chemical: Gramine, tryptamine, Nwmethyl tryptamine and 5methoxyN, NDimethyltryptamine were purchased from Aldrich Chemical Co.
Antialgal test: Test compounds were dissolved in nutrient growth media (Gibco) with the aid of either ultrasound or gentle heating. Chlorella vulgaris from Laboratory of Microbiology, Faculty of Science, University of Chile, Santiago, Chile, was ground in nutrient growth medium. In vitro serial dilutions were prepared in the concentration range from 30 to 1000 μg mL1, with increments of 50 μg mL1. This increment decreased to values from 10 to 20 μg mL1 in the region close to the I50 values. Samples were incubated at 25°C for 10 days in test tubes containing 4.0 x 104 colony forming units (CFU) with continuous cold white fluorescent light with an intensity of 200 ftc. The growth of C. vulgaris was assessed by turbidity measured spectrophotometrically at 600 nm.
Approximate I50 values were obtained from the percentage inhibition according to: I% = 100 (Ts Tc)/(100 Tc) were T is the sample transmittance and Tc the control transmittance.
Germination assays: 20 barley (Hordeum vulgare L.), rye (Secale cereale L., c.v. tetra), wheat (Triticum durum), oat (Avena sativa), Lollium rigidum and 45 lettuce (Lactuca sativa) seeds were uniformly placed on Petri dishes covered with cotton (five Petri dishes by each specie). In order to maintain individual gramine concentration, each plate was watered with 8 mL of an aqueous solution of 0.57and 1.4 mM of gramine. Then, the plates were sealed and incubated at 25± 2°C in an 8h: 16h light:dark cycle for six day. Controls were incubated only with water. Each assay was performed three times. After 6d sowing, germination inhibition of seeds and growth inhibition of shoots were expressed as percentage of the control.
Extract from barley and bioassay
Barley seeds were planted in plastic pots containing sterile soil and were cultivated at 25 ± 2°C under continuous cold white fluorescent light with an intensity of 200 ftc for 12 d. 38 g of grown barley shoots tissue were macerated and diluted in 100 mL of ethanol and allowed to stand for 24 h at room temperature. The macerated was filtered with cheesecloth and evaporated to dryness under reduced pressure. The remaining residue was dissolved in 83 mL of distilled water. Aqueous solution was centrifuged at 4000 g for 25 min. Serial aqueous solutions were prepared in the range of 0.55 to 0.14 mM of gramine from supernatant. Concentration of gramine was determined by HPLC method as previously described (Matsuo et al., 2001). Germination of oat seeds in Petri dishes treated with aqueous solutions from supernatant were developed under the same conditions described as before. After 6d sowing germination inhibition of seeds were expressed as percentage of the control.
RESULTS AND DISCUSSION
Microalgae respond rapidly to environmental changes owing to their short generation time. Green microalgae such as Chlorella are taxonomically classified as plants bearing some similarity to higher plants. For this reason, microalgae tests may be used to evaluate the herbicidal activity against higher plants. Phytotoxicity of indole alkaloids were measured against the fresh water green alga Chlorella vulgaris. I50 values are shown in Table I.
In the concentration range studied (301000 μg mL1), all the tested compounds displayed toxic effects against C. vulgaris. Gramine displays the highest activity and tryptamine is the less active alkaloid. Hansch et al. (1963) proposed a theory to rationalize relations between chemical structure and biological activity of auxins. Their hypothesis assumes that auxins with an aromatic ring and a side chain react with a plant substrate via two points, one on the side chain and the other one on the aromatic ring. Studies on the antialgal activity of indole alkaloids agree with this model. I50 values suggest that, part of phytotoxicity should arise from changes on the length of the side chain and changes on the structure of the amino group. Tryptamine, the less active alkaloid, has two carbon atoms on the side chain without a methyl group in the amino moiety. Gramine, the most active compound, has one carbon atom and a dimethylated amino group. Tryptamine derivatives (mono or dimethylated amino groups) show intermediate activity. Furthermore, more derivatives will be needed to be synthesized in other to clarify the role of the side chain in the phytotoxicity of indole alkaloids.
Phytotoxicity depends on the dose and target species. By the other hand, abiotic and biotic factors can trigger the allelopathic potential of a plant. The effectiveness of an allelochemical is therefore, considered as highly dynamic. Gramine shows the highest antialgal activity; for this reason it was selected to evaluate the phytotoxicity on wheat (T. durum), Rye (S. secaleL.), barley (H. vulgare L.), oat (A. Sativa) lettuce (L. sativa) and the weed Lollium rigidum.
Phytotoxicity was measured from seeds germination and shoot length indicators. In Table 2 the effect of aqueous solution with two different concentrations of gramine on the germination and shoot length for five cultivars and one weed are showed. Germination inhibition indicator (%) displayed more diverse values on the competitive cultivars and allowed a better evaluation of the selective phytotoxicity of gramine. Germination of barley and rye seeds were not inhibited by the two concentrations of gramine studied. Gramine is the main indole alkaloid present on barley that can be released into the environment (Argandoña et al. , 1987). Then, this result suggests that barley has not autotoxicity from gramine and this cereal does not interfere germination of competitive rye cultivar. Germination of wheat and oat seeds was the most inhibited at the two gramine concentrations. Oat was the less tolerant toward gramine.
On the other side, gramine shows a moderate and similar toxicity on lettuce and Lollium rigidum, two smallseeded species. These results could indicate a more diverse phytotoxic selectivity of gramine on the largeseeded crops. Shoot elongation indicator displayed a moderate and less diverse value on all species. Lollium rigidum showed the higher shoot length inhibition (17.2%) at the lower gramine concentration. Rye displays the higher shoot length inhibition effect (29.2%) at the higher gramine concentration studied.
These results may reflect the allelopathic potential of natural occurring indole alkaloids, although the concentrations used are probably greater than in the field. But, the observed effects occur within the range of concentration in which gramine is found in plants (0.2 to 1.6 mmol/Kg Fr wt.) (Matsuo et al., 2001; Argandoña et al., 1987). Part of phytotoxicity in the field can be arising when the allelochemicals are released during the decomposition of competitive cultivars. Therefore, testing the effects of extracts of plant materials should be reasonably adequate assay to compare pure and natural phytotoxic chemical. Gramine is the main indole alkaloid from barley and our results showed that the higher gramine toxicity is produced on oat seed germination, therefore, phytotoxic activity of barley extracts were measured on oat seeds germination. Table 3 shows the germination inhibition (I%) of a series of aqueous solutions in the concentration range of 0.55 to 0.14 mM of natural gramine. Toxic effect decreased in same proportion of a decrease in gramine concentrations. The higher concentration of natural gramine solution (0.55 mM) is similar at the lower concentration of pure gramine solution (0.57 mM) used in the above experiment (Table 2). Both closely displayed toxic effect on the seeds germination (57.0% and 52.6% respectively). According to these results the phytotoxicity of gramine from barley extracts is preserved.
Vainillic and ocoumaric acids along with scopoletin have been suggested that maybe responsible for the allelopathic effects of H. vulgare (Baghestani et al., 1999), our results strongly suggest that part of the allelopathy of barley on competitive cultivars could be also related to the content of gramine in the plant.
Indole alkaloids in cereal species showed toxic activity against microalgae C. vulgaris. Gramine, the main indole alkaloid in barley displayed the highest activity in the studied series. Phytotoxicity measured from seeds germination and shoot length indicators allowed conclude that barley has not autotoxicity from gramine. Moreover gramine does not inhibited germination of rye cultivar. Gramine displayed the highest activity in the germination of wheat and oat seeds. Also gramine displayed a moderate and similar toxicity in the germination of the smallseeded species lettuce and Lollium rigidum. Shoot elongation indicator is moderate and not significant in all species. On the basis of theses results, an allelopathic potential of the natural occurring indole alkaloids is inferred. This is supported from the toxic effect observed of aqueous extract of barley fresh shoot in the germination of oat seeds. Phytotoxic activity is in agreement with the content of gramine in the extracts.
Ahn, J.K., Chung, I. M. (2000) Allelopathic potential of rice hulls on germination and seedling growth of barnyardgrass. Agronomy Journal 92:11621167. [ Links ]
Argandoña, V.H., Zúñiga, G.E., Corcuera, L.J. (1987) Distribution of gramine and hydroxamic acids in barley and wheat leaves. Phytochemistry 26:19171918. [ Links ]
Arnold, G. W., Hill, J. L. (1972) Chemical factors affecting selection of food plants by ruminants. In: Phytochemistry Ecology (Harbone J. B. ed.). Academic Press, New York, pp. 71101 [ Links ]
Baghestani, A., Lemieux, C., Leroux, G. D., Bazirama, keng R., Simard, R.R. (1999) Determination of allelochemicals in spring cereal cultivars of different competitiveness. Weed Science 47:498504. [ Links ]
Batish, D. R., Singh, H. P., Kohli, R. K., Kaur, S. (2001) Crop allelopathy and its role in ecology agriculture. Journal Crop Production 4:121161. [ Links ]
Bravo, H. R., Copaja, S. V., Argandoña, V. H. (2004) Chemical basis for the antifeedant activity of natural hydroxamic acids and related compounds. Journal Agricultural and Food Chemistry 52:25982601. [ Links ]
Burgos, N.R., Talbert, R.E. (2000) Differential activity of allelochemicals from Secale cereale in seedling bioassays. Weed Science 48:302310. [ Links ]
Chou, C.H. (1980) Allopathic researches in subtropical vegetation in Taiwan. Comparative Physiology & Ecology 5:222234. [ Links ]
Copaja, S. V., Villarroel, E., Bravo, H. R., Pizarro, L., Argandoña, V. H. (2006) Hydroxamic acids in secale cereale L. and the relationship with their antifeedant and allelopathic properties. Zeitschrift fur Naturforschung 61C:670676. [ Links ]
Corcuera, L. J. (1984) Effects of Indole Alkaloids from Gramineae on aphids. Phytochemistry 23:539541. [ Links ]
Corcuera, L. J. (1993) Biochemical basis for the resistance of barley to aphids. Phytochemistry 33:741747. [ Links ]
Dias, L. S. (1991) Allelopathic activity of decomposing straw of wheat and oat and associated soil on some crop species. Soil & Tillage Research 21 :113120. [ Links ]
Hansch, C., Muir, R.M., Fujita, T., Maloney, P.P., Geiger, F., Streich, M. (1963) The Correlation of biological activity of plant growth regulators and cloromycetin derivatives with Hammett constants and partition coefficients. Journal American Chemical Society 85:28172824. [ Links ]
Ishikawa, Y., Kanke, T. (2000) Role of gramine in the feeding deterrence of barley against the migratory Iocust, Locusta migratoria (Orthoptera: Acrididae). Applied Entomology and Zoology 35:251256. [ Links ]
Mann, J. D., Steinhart, C.E., Mudd, S.H. (1963) Alkaloids and plant metabolism. Journal Biological Chemistry 238:676681. [ Links ]
Matsuo, H., Taniguchi, K., Hiramoto, T., Yamada, T., Ichinose, Y., Toyoda, K., Takeda, K., Shiraishi, T. (2001) Gramine Increase associated with rapid and transient systemic resistance in Barley seedling induced by mechamical and biological stresses. Plant Cell Physiology 42:11031111. [ Links ]
Miyagawa, H., Toda, H., Tsurushima, T., Ueno, T., Shishiyama, J. (1994) Accumulation of tryptamine in barley leaves irradiated with UV light. Bioscience Biotechnology and Biochemistry 58:17231724. [ Links ]
Overland, L. (1966) The Role of allelopathic substances in the "Smother Crop" Barley. American Journal of Botany 53:423432. [ Links ]
Pastuszewska, B., Smulikowska, S., Wasilewko, J., Buraczewska, L., Ochtabinska, A., Mieczkowska, A., Lechowska, L., Bielecki, W. (2001) Response of animals to dietary gramine I. Performance and selected hematological, biochemical and histological parameters in growing chicken, rats and pigs. International Bibliographic Information on Dietary Supplements 55:116 [ Links ]
Putnam, A.R., De Frank, J. (1983) Use of Phytotoxic plant residues for selective weed control. Journal Crop Protection 2:173181. [ Links ]
Rioboo, C., González, O., Herrero, C., Cid, A. (2002) Physiological response of freshwater microalga (Chlorella vulgaris) to triazine and phenylurea herbicides. Aquatic Toxicology 59:225235. [ Links ]
Sicker, D., Frey, M., Schulz, M., Gierl, A. (2000) Role of natural Benzoxazinones in the survival strategy of Plants. In: International Review of CytologyA survey of Cell Biology. (Jeong K.W. (ed.) Academic Press, San Diego, pp. 319346. [ Links ]
Sicker, D., Schuldz, M. (2002) Benzoxazinones in plants. Occurrence, synthetic access and biological activity. In: Studies in Natural Products Chemistry (AttaurRahman, ed.) Elsevier, Karachi, pp. 185232. [ Links ]
Torres, A., Oliva, R.M., Castellano, D., Cross, P.I. (1996) Introduction. In: Proceedings of the Frirst World Congress on Allelopathyscience for the Future, pp. 7. [ Links ]