An Alternative Approach to the Traditional Mixotrophic Cultures of Haematococcus pluvialis Flotow (Chlorophyceae)


GÖKSAN T., AK İ., Gokpinar S.

JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, cilt.20, sa.9, ss.1276-1282, 2010 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 20 Sayı: 9
  • Basım Tarihi: 2010
  • Doi Numarası: 10.4014/jmb.0909.09005
  • Dergi Adı: JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1276-1282
  • Anahtar Kelimeler: Haematococcus pluvialis, vegetative growth, mixotrophic culture, acetate, pigments, ASTAXANTHIN ACCUMULATION, PIGMENT COMPOSITION, CELL-WALL, GROWTH, GREEN, ALGA, BIOSYNTHESIS, OPTIMIZATION, CAROTENOIDS, IRRADIANCE
  • Çanakkale Onsekiz Mart Üniversitesi Adresli: Evet

Özet

In traditional mixotrophic cultures of microalgae, all the inorganic nutrients and organic carbon sources are supplied in the medium before inoculation. In this study, however, an alternative approach was adopted in Haematococcus pluvialis Flotow, a microalga capable of growing mixotrophically on sodium acetate (Na-Ac). First, the cells were grown under 75 mu mol photons m(-2) s(-1) phototrophically without Na-Ac until the stationary phase and then exposed to five different light regimes by the addition of Na-Ac (e.g., dark, 20, 40, 75, and 150 mu mol photons m(-2) s(-1)). Dry weight (DW), pigments, and especially cell number in alternative mixotrophy (AM) were higher than traditional mixotrophy (TM). Cell number in AM almost doubled up from 21.7 to 42.9x10(4) cells/ml during 5-day exposure to Na-Ac, whereas the increase was only 1.2-fold in TM. Maximum cell density was reached in 75 mu mol photons m(-2)s(-1) among the light intensities tested. We propose that Na-Ac in TM of H. pluvialis can not be utilized as efficiently as in AM. With this respect, AM has several advantages against TM such as a much higher cell density in a batch culture period and minimized risk of contamination owing to the shorter exposure of cells to organic carbon sources. In consequence, this method may be used for other strains of the species, and even for the other microalgal species able to grow mixotrophically.