Excess CO2 supply inhibits mixotrophic growth of Chlorella protothecoides and Nannochloropsis salina.

Mixotrophy can be exploited to support algal growth over night or in dark-zones of a photobioreactor. In order to achieve the maximal productivity, however, it is fundamental also to provide CO(2) in excess to maximize photosynthetic activity and phototropic biomass production. The aim of this paper is to verify the possibility of exploiting mixotrophy in combination with excess CO(2). Two species with high biomass productivity were selected, Nannochloropsis salina and Chlorella protothecoides. Different organic substrates available at industrial scale were tested, and glycerol chosen for its ability to support growth of both species. In mixotrophic conditions, excess CO(2) stimulated photosynthesis but blocked the metabolization of the organic substrate, thus canceling the advantages of mixotrophy. By cultivating microalgae under day-night cycle, organic substrate supported growth during the night, but only if CO(2) supply was not provided. This represents thus a possible method to reconcile CO(2) stimulation of photosynthesis with mixotrophy.

[1]  Deog-Keun Kim,et al.  Effects of SO2 and NO on growth of Chlorella sp. KR-1. , 2002, Bioresource technology.

[2]  Wei Chen,et al.  A high throughput Nile red method for quantitative measurement of neutral lipids in microalgae. , 2009, Journal of microbiological methods.

[3]  G. Singhal,et al.  Function of Photosynthetic Apparatus of Intact Wheat Leaves under High Light and Heat Stress and Its Relationship with Peroxidation of Thylakoid Lipids. , 1992, Plant physiology.

[4]  J. Pittman,et al.  The potential of sustainable algal biofuel production using wastewater resources. , 2011, Bioresource technology.

[5]  Peng Liu,et al.  The effect of mixotrophy on microalgal growth, lipid content, and expression levels of three pathway genes in Chlorella sorokiniana , 2011, Applied Microbiology and Biotechnology.

[6]  İ. Ak,et al.  An alternative approach to the traditional mixotrophic cultures of Haematococcus pluvialis Flotow (Chlorophyceae). , 2010, Journal of microbiology and biotechnology.

[7]  Chunfang Gao,et al.  Double CO(2) fixation in photosynthesis-fermentation model enhances algal lipid synthesis for biodiesel production. , 2010, Bioresource technology.

[8]  Y. Bashan,et al.  Heterotrophic cultures of microalgae: metabolism and potential products. , 2011, Water research.

[9]  F. G. Acién,et al.  Production of astaxanthin by Haematococcus pluvialis: taking the one-step system outdoors. , 2009, Biotechnology and bioengineering.

[10]  L. Gouveia,et al.  A symbiotic gas exchange between bioreactors enhances microalgal biomass and lipid productivities: taking advantage of complementary nutritional modes , 2011, Journal of Industrial Microbiology & Biotechnology.

[11]  W. Cong,et al.  Growth characteristics and eicosapentaenoic acid production by Nannochloropsis sp. in mixotrophic conditions , 2004, Biotechnology Letters.

[12]  Bo Hu,et al.  Oil Accumulation via Heterotrophic/Mixotrophic Chlorella protothecoides , 2010, Applied biochemistry and biotechnology.

[13]  X. Miao,et al.  High quality biodiesel production from a microalga Chlorella protothecoides by heterotrophic growth in fermenters. , 2006, Journal of biotechnology.

[14]  R. Guillard,et al.  Studies of marine planktonic diatoms. I. Cyclotella nana Hustedt, and Detonula confervacea (cleve) Gran. , 1962, Canadian journal of microbiology.

[15]  A. Richmond,et al.  Algal nutrition: heterotrophic carbon nutrition , 2004 .

[16]  J. German,et al.  Photoheterotrophy in the production of phytoplankton organisms , 1999 .

[17]  J. H. Ryther,et al.  Studies of marine planktonic diatoms , 1962 .

[18]  M. Orús,et al.  Interactions between Glucose and Inorganic Carbon Metabolism in Chlorella vulgaris Strain UAM 101. , 1991, Plant physiology.

[19]  Qingyu Wu,et al.  Large‐scale biodiesel production from microalga Chlorella protothecoides through heterotrophic cultivation in bioreactors , 2007, Biotechnology and bioengineering.

[20]  E. Molina Grima,et al.  Comparison between extraction of lipids and fatty acids from microalgal biomass , 1994 .

[21]  J. Waterbury,et al.  Generic assignments, strain histories, and properties of pure cultures of cyanobacteria , 1979 .

[22]  Yanna Liang,et al.  Biomass and lipid productivities of Chlorella vulgaris under autotrophic, heterotrophic and mixotrophic growth conditions , 2009, Biotechnology Letters.

[23]  Hans Ulrich Bergmeyer,et al.  Methods of Enzymatic Analysis , 2019 .

[24]  L. Rodolfi,et al.  Microalgae for oil: Strain selection, induction of lipid synthesis and outdoor mass cultivation in a low‐cost photobioreactor , 2009, Biotechnology and bioengineering.

[25]  A. Bloom,et al.  CO(2) Inhibits Respiration in Leaves of Rumex crispus L. , 1992, Plant physiology.

[26]  Y. Chisti Biodiesel from microalgae beats bioethanol. , 2008, Trends in biotechnology.

[27]  Jeffrey Philip Obbard,et al.  Two phase microalgae growth in the open system for enhanced lipid productivity , 2011 .

[28]  E. Sforza,et al.  Vegetal oil from microalgae: species selection and optimization , 2010 .

[29]  C. Foyer,et al.  Use of mitochondrial electron transport mutants to evaluate the effects of redox state on photosynthesis, stress tolerance and the integration of carbon/nitrogen metabolism. , 2003, Journal of experimental botany.

[30]  J. Pronk,et al.  Fed-batch cultivation of the docosahexaenoic-acid-producing marine alga Crypthecodinium cohnii on ethanol , 2003, Applied Microbiology and Biotechnology.