The effects of mixed carbon sources on growth and production of vitamins E and A by Euglena gracilis cells were investigated in batch culture. The cells were grown mixotrophically in glucose (G), ethanol(E) and a mixture of glucose and ethanol (EG). Cell growth was measured by counting the cell number with microscope, while vitamin concentrations were measured spectrophotometrically. Growth of thecells was found to be much better in the mixed carbon culture (EG) than in either glucose (G) or ethanol (E) alone. Significance difference was detected (P  [G] > [E].The average cell density in the mixed carbon culture reached 2.34 ± 0.109 x 107 cells/ml after 7 days. It was about 1.63 ± 0.089 x 107 cells/ml in glucose and 0.70 ± 0.084 x 107 cells/ml in ethanol. The result also showed that ethanol alone was the best carbon source for production of the vitamins. The results indicated that the mixed carbon culture enhanced growth of the cells, but cellular contents of theantioxidant vitamins were low. Thus, the mixed substrate system has a high potential for large-scale production of Euglena biomass

Afiukwa, CA

Ogbonna, JC

English

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  African Journal of Biotechnology Vol. 6 (22), pp. 2612-2615, 19 November, 2007 Available online at http://www.academicjournals.org/AJB ISSN 1684–5315 © 2007 Academic Journals    Full Length Research Paper  Effects of mixed substrates on growth and vitamin production by Euglena gracilis  Celestine A. Afiukwa* and James C. Ogbonna  Department of Biochemistry/Biotechnology, Faculty of Applied and Natural Sciences, Ebonyi State University, P. M. B. 053, Abakaliki, Nigeria.  Accepted 16 October, 2007  The effects of mixed carbon sources on growth and production of vitamins E and A by Euglena gracilis cells were investigated in batch culture. The cells were grown mixotrophically in glucose (G), ethanol (E) and a mixture of glucose and ethanol (EG). Cell growth was measured by counting the cell number with microscope, while vitamin concentrations were measured spectrophotometrically. Growth of the cells was found to be much better in the mixed carbon culture (EG) than in either glucose (G) or ethanol (E) alone. Significance difference was detected (P < 0.05) on cell growth and ranked as [EG] > [G] > [E]. The average cell density in the mixed carbon culture reached 2.34 ± 0.109 x 107 cells/ml after 7 days. It was about 1.63 ± 0.089 x 107 cells/ml in glucose and 0.70 ± 0.084 x 107 cells/ml in ethanol. The result also showed that ethanol alone was the best carbon source for production of the vitamins. The results indicated that the mixed carbon culture enhanced growth of the cells, but cellular contents of the antioxidant vitamins were low. Thus, the mixed substrate system has a high potential for large-scale production of Euglena biomass.  Key words: mixed substrate culture, Euglena gracilis, cell growth, vitamin production.    INTRODUCTION  The role of Euglena gracilis as a good source of nutrition-ally and medically important substances has called for more research on how to maximize its production. The main importance of E. gracilis is that it contains high amounts of proteins, vitamins and polyunsaturated fatty acids (PUFAs). Consequently, it is used as health food and animal feed. Antioxidant vitamins such as α-tocophe-rol, L-ascorbic acid and β-carotene, which function to prevent diseases caused by oxidative damages among other functions, are accumulated in significant amounts by E. gracilis (Takeyama et al., 1997). Although many higher plants are known to produce these vitamins, their production in photosynthetic microorganisms is much higher owing to higher growth rates and absence of sea-sonal influences, which make it possible for the cells to be cultivated all year round. Polyunsaturated fatty acids (PUFAs), especially linoleic and α-linolenic acids, which have a  number  of  physiolo-    *Corresponding author. E-mail: afiukwa@yahoo.com. gical functions, have also been reported to be produced in significant amounts by the microorganism (Hayashi et al., 1993).  PUFAs are important in the body for synthesis of membrane lipids, reduction of blood cholesterol levels, reduction of risk of heart attack, normal development of brain and retina and for synthesis of other physiologically important substances like prostaglandins (Taylor et al., 1998a). It is known that fishes, the major sources of PUFAs, obtain these fatty acids from photosynthetic cells in a food chain. E. gracilis is among the many photosynthetic micro-organisms employed for production of single cell protein (SCP), a new food source, used as an alternative source of proteins in developed countries like Europe, America and Asia. Protein remains the most costly food compo-nent in countries like Nigeria, where SCP technology has either not been adopted or developed to supplement the conventional sources, such as meat, eggs, fishes and legumes. SCP from photosynthetic cells (algae) is consi-dered better than those from bacteria or fungi. This is because, algae including E. gracilis, accumulate less amounts of nucleic acids than bacteria and fungi. High le-        vels of nucleic acids increase the risk of occurrence of a disease condition known as gout. Furthermore, photosynthetic cells, have been recogni-zed as a potential tool for environmental bioremediation because of their ability to metabolize toxic substances such as nitrogen and sulphur oxides (Negoro et al., 1991; Yoshihara et al., 1996; Ogbonna et al., 2002), and for production of biological fuels (Zarborsky et al., 1998; Kishimoto et al., 1994; Yamaberi et al., 1998; Taylor et al., 1998b). E. gracilis is capable of growing as a strict photo-autotroph, a photoheterotroph or a strict heterotroph lacking differential chloroplasts (Osafune et al., 1990). Although antioxidant content in cells grown under photo-autotrophic conditions is higher, biomass production under photoheterotrophic or heterotrophic conditions is higher (Shigeoka et al., 1980; Hosotani and Kitaoka, 1984). A mixed substrate culture is one that contains a multi-ple sources of nutrients that serve a similar physiological function. For example, a culture containing both glucose and ethanol as carbon sources is a mixed substrate culture. It has been recognized as a technique for yield improvement (Bull, 1985). Glucose has been identified as the best carbon source for biomass production in E. gracilis while ethanol was the best for α-tocopherol pro-duction (Ogbonna et al., 1998). It was against this background that this study was initiated with the aim of developing a new culture system for efficient production of E. gracilis biomass. We expected that the high growth of the cells observed in glucose and high α-tocopherol content in ethanol would be integrated in cells grown in a mixture of the two carbon sources.   MATERIALS AND METHODS  Microorganism and media composition   E. gracilis z was obtained from the culture collection centre of the Institute of Applied Microbiology, University of Tokyo, Japan and subcultured at OGB Biotechnology Research and Development Centre Enugu, Nigeria. Three types of media, labeled G, E and EG on the basis of carbon sources, were used. G contained glucose (10 gl-1), E contained ethanol (10 gl-1), while EG contained a mixture of glucose and ethanol (10 gl-1 of each) as carbon sources. Also added was a source of mineral elements, liquid fertilizer (2.5 ml l-1). The fertilizer (Boost xtra foliar fertilizer complex from Candel) was composed of nitrogen (20%), potassium (20%), phosphorus (20%), magnesium (1%), manganese EDTA (0.075%), copper EDTA (0.075%), cobalt EDTA (0.0012%), zinc EDTA (0.075%), iron (0.15%), boron (0.0315%) and molybdenum (0.0012%). The media were sterilized by autoclaving at 121oC for 15 min.   Effect of mixed carbon sources on cell growth  Erlenmeyer flask (500 ml) containing 100 ml of the medium was used for the cultures. It was equipped with a high quality foam plug and a narrow heat resistant  plastic  tube  passed  into  the  medium  Afiukwa and Ogbonna        2613    through the plug and extends to the outside for aseptic collection of samples for analysis. The exterior opening of the narrow tube was sealed with masking tape. Approximately 0.5 ml of a pure culture of E. gracilis was asep-tically transferred into the medium in a clean box and then incubated at room temperature (25oC) indoors, between two parallel daylight fluorescent tubes (T9 18 watt, 220 – 240 V). The distance of flask from the light source was 5 cm. Cell growth was measured daily for a period of one week by counting the cell number with microscope and Neubaur counting chamber. Growth of the cells was determined in the three media to investigate the effect of the combined carbon sources by comparing the plots of their time courses of growth.   Effect of mixed carbon sources on production of vitamins E and A  Erlenmeyer flask (500 ml) was also used for the cultures as des-cribed above. The intracellular concentrations of the vitamins were determined spectrophotometrically using the method described by David (1978). A known volume of the culture was centrifuged at 3000 rpm for 10 min. The supernatant was discarded and the pellet washed with distilled water. Acetone (5 ml) was added and allowed to stand for 10 min to extract the cell contents. This was necessary because most of the vitamins are contained inside the cells. Distilled water (2 ml) and 5 ml of petroleum ether were then added. There was a separation of oily layer on top of the aqueous liquid. The top layer was gently collected with pipette and used to determine the concentration of the fat soluble vitamins E and A by reading their absorbance at 450 nm and 493 nm respectively, with spectrophotometer model 722S. The dry weight of the cells used in the process was predetermined by counting the cell number in the broth and estimating the corresponding dry weight from a calibration curve. The cellular con-centration of the vitamins were then calculated from the equation,   Conc. (mg/g) = (A x DF) / (Ext. Coeff. x light path x wgt)  A = absorbance, DF = dilution factor, Ext. Coeff = absorption, Coefficient (1026 for vitamin E and 2592 for vitamin A in mg-1cm-1ml), light path = thickness of cuvette (usually 1 cm) and wgt = dry weight of cells used (gml-1).   Determination of glucose and ethanol concentrations  Glucose kit (Quimica clinica Aplicada S.A., Amposta, Spain) was used to measure glucose concentration daily throughout the period of cultivation. Ethanol concentration was measured using the boiling/iodometric method (Gwarr, 1987).   RESULTS  Effect of mixed carbon sources on cell growth and vitamin production  The effect of a mixture of glucose and ethanol on growth of E. gracilis cells is shown in Figure 1. The growth of the cells was better in the mixed substrate medium (EG) than in either of the single substrate media, G or E. The figure also showed that the cells grew better in glucose than in ethanol. Statistical analysis of  the  result  using  the  LSD    2614           Afr. J. Biotechnol.    0.00.51.01.52.02.50 2 4 6 8Cultivation time (days)Cell number (x 10 7 /ml)GEEG  Figure 1. Effect of mixed substrates on growth of Euglena gracilis.    00.10.20.30.40.50 2 4 6 8Cultivation time (days)Vitamin E conc. (mg/g dry cell) GEEG  Figure 2. Effect of mixed substrates on vitamin E production by Euglena gracilis.    value at 95% confidence level showed a ranking order of (EG) > (G) > (E). As shown in Figures 2 and 3, the combination of glucose and ethanol had no advantage on production of the vitamins under the culture conditions used. Ethanol alone was better for intracellular content of the vitamins than either glucose alone or the combination.   Utilization of glucose and ethanol in the mixed carbon culture      This study was carried out to help us understand the cause of the rapid cell growth obtained in the mixed carbon culture. The result (Figure 4) showed that the con-centration of the two substrates declined simultaneously with time in the mixed carbon culture. This indicates that the cells utilized both substrates simultaneously.      00.010.020.030.040.050 2 4 6 8Cultivation time (days)Vitamin A conc. (mg/g dry cell) GEEG  Figure 3. Effect of mixed substrates on vitamin A production by Euglena gracilis.      Figure 4. Pattern of utilization of glucose and ethanol by Euglena gracilis in a mixed carbon culture.    DISCUSSION  Mixed substrate culture has been recognized as a techni-que for yield improvement in microbial cultivations. Con-sequently, culture media for industrial fermentations are frequently formulated so that they contain complex mixture of nutrients, and mixed carbon sources in particu-lar have been exploited for improvement of antibiotic yields (Bull, 1985). In this work, the growth of E. gracilis was found to be enhanced by the mixed substrate system relative to either of the single substrate cultures. The actual cause of the rapid cell growth observed in the combined substrate culture is not precisely known. However, one of the possible reasons may be due to simultaneous utilization of the two carbon sources. It has been  reported  that  some  microorganisms  utilize  some       substrate mixtures simultaneously. For example, Kluvero-myces fragilis has been reported to utilize glucose and fructose simultaneously (Bull, 1985). The result of the study on pattern of consumption of the two substrates in the mixed carbon culture (Figure 4) showed that the glucose and ethanol were simultaneously utilized by E. gracilis. However, the rate of consumption of ethanol was higher than that of glucose. About 6.0 gl-1 of ethanol was consumed in 7 days, but only about 4.9 gl-1 of glucose was consumed during the same period. This agrees with a report that when ethanol and glucose were added simultaneously to a culture of E. gracilis at a concentra-tion of 1.0% respectively, ethanol was consumed more rapidly than glucose (Tani and Tsuruma, 1989). Simulta-neous utilization of substrates may occur when the substrates are catabolized via different metabolic path-ways. Glucose is catabolized by most microorganisms through two major routes; glycolytic and pentosphos-phate pathways (Okafor, 1987). Ethanol, on the other hand, is also catabolized through two routes, the alcohol dehydrogenase and the  glyoxylate pathways (Ono et al., 1995). Simultaneous utilization of substrates may also occur when one of the component substrates in the mixture is required by the cells for production of certain metabolites (Bull, 1985). Reports exist that E. gracilis requires ethanol as a precur-sor for α-tocopherol production (Ogonna et al., 1998). The results of vitamin production (Figures 2 and 3) showed that there was no advantage of the mixed substrate system on production of the vitamins tested under the culture conditions used. We suspect that one of the possible reasons may be that the resulting high cell density in the mixed carbon culture limited light distribu-tion among the cells in the culture. This situation is known to affect the accumulation of light dependent metabolites such as α-tocopherol (Ogbonna et al., 1997; Ogbonna and Tanaka, 2000; Ogawa and Aiba, 1981). It is therefore important to investigate the effect of light intensity on mixed substrate cultivation of E. gracilis.  Cultivation of micro algae just for production of vitamins or proteins is very expensive and not economically feasi-ble. However, the fact that the microorganism simultane-ously produces a number of useful metabolites such as protein, vitamins, PUFAs and carbohydrates, which could be isolated separately, makes the process potentially economical. Besides, unlike higher plants and animals (conventional sources of the useful metabolites) micro-organisms generally require much less space and could be grown all year round since they are not affected by seasonal and environmental changes. Its development could therefore guarantee steady supply of the useful products.    REFERENCES  Bull AT (1985).  Mixed  culture  and  mixed  substrate  system,  compre- Afiukwa and Ogbonna        2615    hensive Biotechnology 1: 281-299, Pergamon press, New York. David P (1978). Chemical analysis of food, Churchill Livingstone. pp 130-140. Gwarr SG (1987). Measurement of ethanol concentration. In: Ezeogu LI, Okolo BN, Ogbonna JC (2005). 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Effects of mixed substrates on growth and vitamin production by Euglena gracilis

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Effects of mixed substrates on growth and vitamin production by Euglena gracilis

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