Abstract
Microalgae are a renewable natural resource that requires only sunlight, carbon dioxide, phosphorus, and nitrogen for rapid growth. They produce a broad variety of basic chemical substances―such as vitamins, fatty acids and carotenoids-that have high added value potential for the pharmaceutical and food industries. The aim of this study was to develop axenic culture and to establish a cell growth assay for microalgae. A further experiment was carried out to determine the yield of astaxanthin derived from microalgae. The axenic culture was developed using a mixture of antibiotics [ampicillin (100 μg/ml), streptomycin (10 μg/ml), chloramphenicol (10 μg/ml), penicillin (10 μg/ml), neomycin (50 μg/ml), gentamycin (50 μg/ml), kanamycin (10 μg/ml), and nystatin (1.5 μg/ml)] and then used to extract a variety of useful components from the microalgae. The optimal concentration for the antibiotic mixture was 1-3 percent. A spectrophotometric cell growth assay was also established. Astaxanthin was extracted from Haematococus lacustris with a yield of 1.9×10-3 μg/l per 1 ml of culture medium. In conclusion, the axenic culture method developed here allows extraction of high-quality astaxanthin and other useful components from microalgae.
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CITATION STYLE
Son, M. C., Lee, D.-J., Park, S., Kim, M. S., Lee, C. W., & An, W. G. (2015). Development of Axenic Culture and Astaxanthin Production in Microalgae. Journal of Life Science, 25(7), 733–739. https://doi.org/10.5352/jls.2015.25.7.733
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