Establishment and maintenance of an axenic culture of Ettlia sp. using a species-specific approach
Autor: | Chi-Yong Ahn, Ankita Srivastava, Hee-Mock Oh, Hee-Sik Kim, Hyung-Gwan Lee, Sang-Yoon Shin, Chan Yoo, Long Jin, Hyun-Joon La |
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Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
Ettlia Serial dilution biology Microorganism Chloramphenicol 030106 microbiology Biomedical Engineering Bioengineering biology.organism_classification Applied Microbiology and Biotechnology Microbiology Agar plate 03 medical and health sciences 030104 developmental biology medicine Subculture (biology) Axenic Temperature gradient gel electrophoresis Biotechnology medicine.drug |
Zdroj: | Biotechnology and Bioprocess Engineering. 20:1056-1063 |
ISSN: | 1976-3816 1226-8372 |
DOI: | 10.1007/s12257-015-0289-4 |
Popis: | The establishment of an axenic culture of microalgae is essential step in understanding its physiology, genetics, and ecology. However, culturing of microalgae is usually accompanied by complex and variable associated prokaryotic and eukaryotic microorganisms. Conventional approaches used for obtaining axenic cultures of microalgae are time-consuming and often involve difficulties in maintaining and preserving axenicity. In this study, we developed a procedure for establishing an axenic culture of Ettlia sp. YC001 and demonstrate that we maintained the axenic culture through subculture in the long term. Three sequential treatments, an antibiotic cocktail, serial dilution, and plate spreading, were applied to strain YC001 and we confirmed axenicity using molecular and physiological methods. The bacterial community associated with strain YC001 was investigated to select antibiotics for their specific elimination. The xenic culture (1 × 106 cells/mL) was treated with the antibiotic cocktail-5 (AC-5), carbendazim, chloramphenicol, imipenem, rifampicin, and tetracycline for 3 days, followed by serial dilution up to 1 × 102 cells and spreading on agar plates. The pure colonies were analyzed using denaturing gradient gel electrophoresis (DGGE), fluorescence-activated cell sorting (FACS), and scanning electron microscopy (SEM). The procedure we developed can be applied to other strains of microalgae for the establishment of axenic cultures. |
Databáze: | OpenAIRE |
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