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versión On-line ISSN 0717-7178
Investig. mar. v.35 n.2 Valparaíso nov. 2007
Invest. Mar., Valparaíso, 35(2): 63-69, 2007
Chemical constituents of Eisenia arbórea Areschoug from Baja California Sur, México
Constituyentes químicos de Eisenia arbórea Areschoug de Baja California Sur, México
Dora L. Arvizu1, Yoloxochitl E. Rodríguez1, Gustavo Hernández1 & Jesús I. Murillo1
1Centro Interdisciplinary de Ciencias Marinas-IPN, Departamento Desarrollo de Tecnologías. Apdo. Postal 592. La Paz, B.C.S., México, 23000
ABSTRACT. Samples of Eisenia arbórea from Baja California Sur, México collected in November 2002 and March 2003 were studied. The following parameters were analyzed separately from blades and stipes: moisture, ash, mannitol, fat and crude fiber. Alginate was isolated and the following quality parameters were obtained: yield (22.4-23.3%), color (> 4) and viscosity (793- 2,210 m-Pa-s in 1% solution). No significant differences were obtained between two months, except for viscosity and crude fiber. Significant differences were obtained when comparing blades and stipes in viscosity, mannitol, ash and fat, while for yield, moisture and crude fiber no significant differences were obtained. FTIR spectroscopy showed that alginate from E. arbórea contained similar amounts of mannuroic and guluronic acids (M/G = 1).
Key words: alginate, Eisenia arbórea, guluronic acid, mannuroic acid, mannitol, fat, crude fiber.
RESUMEN. Se estudiaron muestras de Eisenia arbórea de Baja California Sur, México, recolectadas en noviembre de 2002 y marzo de 2003. Se determinaron los siguientes parámetros en lámina y estipe: humedad, cenizas, manitol, grasas y fibra cruda. Se aisló el alginato y se obtuvieron los siguientes parámetros: rendimiento (22,4-23,3%), color (> 4) y viscosidad (793-2.210 m-Pa-s en una solución al 1%). No se encontraron diferencias significativas entre los dos meses, a excepción de la viscosidad y fibra cruda. Se obtuvieron diferencias significativas al comparar los resultados entre lámina y estipe en viscosidad, manitol, cenizas y grasas, mientras que en el rendimiento, humedad y fibra cruda no hubo diferencia significativa. El espectro FTIR mostró que los alginatos de E. arbórea contenían una cantidad similar de ácidos manurónico y gulurónico (M/G = 1).
Palabras clave: alginato, Eisenia arbórea, ácido gulurónico, ácido manurónico, manitol, grasas, fibra cruda.
Marine algae are one of the main renewable resources of the Baja California Peninsula. One of the main groups is the Phaeophyta because of its abundance and high content of alginates, mannitol, iodine and fucoidan. In this group we found the species Macro-cystis pyrifera (Linnaeus) C. Agardh and Sargassum spp, which have been widely studied. However, there is another kelp type and abundant species, Eisenia arbórea Areschoug which has been very little studied. This species is distributed from British Columbia, Canada (Druehl, 1970) to Magdalena Bay, Baja California Sur, México (Aguilar-Rosas et al, 1990). This kelp is found from the intertidal level to 34 m depth, forming dense beds in many rocky areas along the Pacific coast, and produces shade to understory algae (Spalding et al., 2003).
The main interest of brown seaweeds from an industrial point of view is their alginate content. Alginate is a polysaccharide found in the cell wall as structural component of the alga and it is used for its thickening, stabilizing, film-forming and gel-producing properties (Kelco, 1986; Lobban & Harrison, 1994). The use of Eisenia arbórea as food complement will depend on its chemical composition. It could be used for example as a food complement for poultry, cattle or even man (Marín et al., 2003). In most of the algae, alginate yield and other chemical compounds do not remain constant and we may expect some seasonal variation or differences depending on the part of the algae used. These variations may change from place to place and could be related to environmental parameters (Percival & McDowell, 1967).
There is not enough published information about Eisenia arbórea chemical composition or the alginate properties from it. The objective of this study was to determine some chemical constituents, alginate yield and quality from E. arbórea from Magdalena Bay, B.C.S. and analyze its potential as raw material for alginate production.
MATERIALS AND METHODS
Samples oí Eisenia arbórea were collected in Punta El Cabito del Farallón (24°33' 24.4"N, 112°06' 07.1"W) near Magdalena Bay, in November 2002 and March 2003 between 10-15 m depth. Algae were obtained at random, using one square meter quadrat (n = 30). Plants were cut with a knife from the base of the holdfast. The population consisted of adult plants with a density of 19 plantsm"2, with about the same size (88.7-122.6 cm) and weight (633-748 g). We assume that our sample included reproductive and sterile plants.
Alginate yield, viscosity and color
Algae were separated into blades and stipes, dried directly in sunlight and milled to 30 mesh. Alginate extraction at the laboratory level was carried out according to the method proposed by Arvizu-Higuera et al. (2002). Alginate yield was calculated based on the initial dry weight of the sample. Apparent viscosity was measured in 1% alginate solution at 22°C, using a viscosimeter Brookfiel LVT. Color was by comparison with color standard in a scale of 1 to 4 (Hernández-Carmonaeía/., 1999a).
The following methods were used: moisture by ther-mo balance; ashes by ignition in a furnace (AOAC, 1990); mannitol by fast oxidation of poliol with periodic acid (Larsen, 1978); fat by microwave-assisted process (MAPTR), using a mixture of the solvents diethyl ether-acetone in proportion 2:1 (Paré et al., 1994) and crude fiber by acid and alkaline hydrolysis (Larsen, 1978).
All the experiments were carried out in triplicate. The average, standard error and confidence interval (± SE), with a level of significance at 95% were computed. ANOVA was used to detect significant differences between the two samples and parts of the plant (p < 0.05) and Tukey honest significant test was used for post-hoc comparison of means (Zar, 1999).
Alginate composition by infrared spectroscopy
For IR spectral analysis, the alginate samples obtained above (blade and stipe of November and March) were separately dissolved in distilled water (5 mg-rnL-1). Two milliliters of each solution were transferred to polyethylene molds and evaporated to dryness at 55°C for 12 h. Each transparent alginate film was mounted between two papers cut in a convenient shape for analysis. The spectra were acquired in a spectrometer FTIR Nicolet Avatar 360. All IR spectra were obtained in transmission on the spectral range of 400-500 cm-1. Each spectrum was the average of 128 scans at 4 cm-1 resolution. The M/G ratio (Mannuronic/Guluronic) was estimated semi-quantitatively by comparison of the relative intensity of the IR bands against a standard. The method of most probable base line was used to calculate the relative intensity of IR absorption bands.
The alginate used as standard was subjected to compositional analysis by 1HNMR according with the protocol proposed by Grasdalen et al. (1979), and characterized by FTIR spectroscopy, as well. The sample for NMR was dissolved in D20. The spectrum was recorded at 300.13 MHz with a Jeol FX-300 FT-NMR spectrometer (USA).
Alginate yield, viscosity and color
Alginate yield was not significantly different between structures nor between two months (p > 0.05). Yield for blades was 22.9% in November and 22.7% in March. Yield for stipes was 23.3% in November and 22.4% in March (Fig. 1). Viscosity of alginates obtained was significantly different between blades and stipes (p < 0.05). Alginate viscosity from blades was 37% higher than stipes during November, and 43% higher than stipes in March. Alginate viscosity from stipes increased from November (793 ± 67.2 m-Pa-s) to March (1,260 ± 236.3 m-Pa-s), which represented a difference of 37%. Alginate viscosity from blades increased from November (1,270 ± 143.3 m-Pa-s) to March (2,210 ± 232.2 m-Pa-s), which represented a difference of 42%. In all cases, alginate color was higher than 4, according to the standards used, however alginate from stipes was slightly lighter than alginate from blades.
Results are shownin Fig. 1. Eisenia arbórea moisture content after sun drying ranged from a maximum of 17.7% in stipes from November to a minimum of 10.4% on stipes from March. Moisture in blades was not significantly different (10.4-11.7%, p > 0.05). Ash content was not significantly different by sampling month, but it was different between structures in November (38.7% in stipes and 31.8% in blades). Mannitol content was significantly different (p < 0.05) only between structures sampled from November. Maximum values were obtained on stipes (11.1%) and minimum on blades (5.7%). Fat content in November was significantly higher (p < 0.05) in blades (1.28%) than stipes (0.82%), while March samples were not significantly different (p > 0.05) in both structures (0.97 and 0.98%). Crude fiber from samples collected in March was significantly higher (p < 0.05) in stipes (7.7%) than blades (5.7%). Crude fiber values in November were significantly lower (p < 0.05), ranging from 4.2% in stipe to 5.2% in blades.
Alginate composition by infrared spectroscopy
Figure 2 shows the dactiloscopic region (1,470-750 cm-1) of the IR spectra of the blades from November (B-Nov), stipes from November (S-Nov), blades from March (B-Mar), and stipes from March (S-Mar). The four spectra showed absorption bands that correspond to bands assigned to sodium alginate. Table 1 shows the comparison of the relative intensity of IR bands from our samples against the relative intensity of bands of an alginate with a known M/G ratio, this suggest that the M/G ratio for our samples was about 1. The 1HNMR spectrum of the alginate (Fig. 3) used as standard showed frequencies of mannuronic and guluronic acids to be 0.52 and 0.48, respectively. The M/G ratio was 1.08, and the length of the monoguluronic blocks was 7 units.
Using the comparison of relative intensities of IR bands of alginates isa semi-quantitative approach, so it was not possible to detect differences of M/G ratio from seasons or structures, because the differences were very low (Table 1).
Alginate yield was lower that obtained by Hernández-Carmona (1985) (24.6-28.6%) with the same species and collected at a location close to our sampling area, however, he did not find either a significant seasonal variation of alginate yield. The yield obtained in this study was lower than in Eisenia bicyclis (Kjellman) Setchell with 34% (Asakawa et al, 1984).
The alginate viscosity in March for blades was double the viscosity reported for Macrocystis pyri-fera with 1,016 m-Pa-s (Hernández-Carmona et al., 1999b). Since alginate is a structural polysacchari-de, this may explain the high resistance of Eisenia arbórea to strong currents and swell common in Magdalena Bay, which are stronger in winter (Martinez-Lopez & Verdugo-Díaz, 2000).
The alginate color obtained from Eisenia arbórea was dark brown, and gave a higher value that commercial standard (1-4). However, the color could be improved using an additional step of bleaching in the extraction process of alginate, as it is generally carried out at the industrial level.
The moisture of all samples was under the maximum moisture recommended (12%), except for the stipes from November. It means that alga drying was enough to avoid decomposition so it can be transported and stored for long time periods.
Ash values obtained in November and March for stipes and blades were similar to values obtained for Eisenia bicyclis (33.2%) (Asakawa e? a/., 1984). In general, ash content is always reported as high content in other brown algae (Larsen, 1978; Kelco, 1986; Rodríguez-Montesinos & Hernández-Carmo-na, 1991; Pérez-Reyes, 1997).
Mannitol changes are correlated with plant growth and reproductive condition (Lobban & Harrison, 1994). The highest value for Eisenia arbórea was obtained in March; however it is lower than in E. bicyclis (12.9%) (Asakawa et al, 1984), but it was higher than Macrocystis pyrifera in winter (7.3-8.2%) (Rodríguez-Montesinos & Hernández-Carmona, 1991).
In general, the fat content in brown algae is very low. For this study, the values were similar to other genus like Laminaria (0.2-3%) (Chapman & Chapman, 1980) and Macrocystis (0.5-2.3%) (Ortega-Ceseña & Zaragoza-García, 1983; Kelco, 1986; Rodríguez-Montesinos & Hernández-Car-mona, 1991).
The values of crude fiber in this study were higher than obtained in Eisenia bicyclis (1.6%) (Asakawa et al., 1984), but similar to Ascophyllum nodosum (Linnaeus) Le Jolis (5%) and Laminaria digitata (Hudson) J.V. Lamouroux (7%) (Guiry & Blunden, 1991).
The alginate IR spectra showed absorptions which were consistent with sodium alginate extracted from Laminaria hyperborea. Sodium alginate can easily be distinguished from calcium alginate because differences into band shift (Sartori et al., 1997). In addition to the cation content, the man-nuronic/guluronic proportion can be inferred in a semi-quantitative approach from the relative intensity ratio of characteristic IR bands. In general, alginate with high content of guluronic units produced more intense bands (Table 1) than alginate with medium content of guluronic units (Sartori et al., 1997; Pereira et al., 2003). NMR methods are the best in order to determine the detailed compositional data of alginate samples, but these methods are high in cost. The infrared spectroscopy presents four main advantages: it is not as expensive as NMR methods, it is fast, non-destructive, and it requires small sample quantities, which makes it quite convenient for rapid characterization of cation content and M/G proportion in alginate. Unfortunately, no obvious differences can be observed in the IR spectra as a function of molecular weight or length of monoblocks.
This study gives us basic information about Eise-nia arbórea, abundant species in the Baja California Peninsula coasts. According the results obtained the blades had better quality of alginate, however, a more detailed study is needed, manly about its biomass to get a reliable conclusion if this specie could be exploited for commercial use.
The authors are grateful to Instituto Politécnico Nacional (CICIMAR-IPN) for the financial support. We are grateful to the "Comisión para el Fomento de Actividades Académicas del Instituto Politécnico Nacional (COFAA-IPN)" and the Program "Estímulo al Desempeño de la Investigación (EDI-IPN)" for the fellowship received. We thank to "Dirección de Servicios Periciales de la Procuraduría General de Justicia" of Baja California Sur State, for allow us to use the FTIR spectrophotometer equipment. We thank to Kim Siewers for English edition.
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Received: 12 February 2007; Accepted: 6 September 2007
Corresponding author: Dora L. Arvizu (firstname.lastname@example.org)