A Rare Phaeodactylum tricornutum Cruciform Morphotype: Culture Conditions, Transformation and Unique Fatty Acid Characteristics

A rare Phaeodactylum tricornutum cruciform morphotype was obtained and stabilized with a proportion of more than 31.3% in L1 medium and is reported for the first time. Long-term culture and observation showed that the cruciform morphotype was capable of transforming to the oval form following the degeneration of arms by two processes. After three months of culture, four morphotypes existed in a relatively stable proportion in culture for six months (10.5% for oval, 11.3% for fusiform, 37.2% for triradiate and 41.0% for cruciform). Low temperature was particularly beneficial for cruciform cell formation. As the culture temperature decreased from 25°C to 10°C, the percentage of the cruciform morphotype increased from 39.1% to 55.3% approximately. The abundant cruciform cells endowed this strain with unique fatty acid characteristics. The strain cultured at 15°C showed both maximum content of neutral lipid in a single cell and total yield. The maximum content of fatty acid methyl esters was C16:1 for Phaeodactylum tricornutum cultured at four temperatures (43.82% to 50.82%), followed by C16:0 (20.47% to 22.65%). Unique fatty acid composition endowed this strain with excellent quality for biodiesel production.

[1]  M. S. Cooper,et al.  Visualizing "green oil" in live algal cells. , 2010, Journal of bioscience and bioengineering.

[2]  Liang-ping Lin,et al.  Morphology and eicosapentaenoic acid production by Monodus subterraneus UTEX 151. , 2005, Micron.

[3]  C. Bowler,et al.  Physiological and molecular evidence that environmental changes elicit morphological interconversion in the model diatom Phaeodactylum tricornutum. , 2011, Protist.

[4]  Nicolas Carels,et al.  Genome Properties of the Diatom Phaeodactylum tricornutum 212 , 2002, Plant Physiology.

[5]  R. Carlson,et al.  Potential role of multiple carbon fixation pathways during lipid accumulation in Phaeodactylum tricornutum , 2012, Biotechnology for Biofuels.

[6]  W. J. Dyer,et al.  A rapid method of total lipid extraction and purification. , 1959, Canadian journal of biochemistry and physiology.

[7]  F. Brun,et al.  Monitoring the long-term stability of pelagic morphotypes in the model diatom Phaeodactylum tricornutum , 2011 .

[8]  Rupam Kataki,et al.  Microalgae Chlorella as a potential bio-energy feedstock , 2011 .

[9]  T. Brembu,et al.  Gene Regulation of Carbon Fixation, Storage, and Utilization in the Diatom Phaeodactylum tricornutum Acclimated to Light/Dark Cycles1[C][W][OA] , 2012, Plant Physiology.

[10]  F. Ojeda,et al.  Phenotypic response of the diatom Phaeodactylum tricornutum Bohlin to experimental changes in the inorganic carbon system , 2008 .

[11]  V. Martin‐Jézéquel,et al.  Insights into the polymorphism of the diatom Phaeodactylum tricornutum Bohlin , 2009 .

[12]  S. Rombauts,et al.  The metabolic blueprint of Phaeodactylum tricornutum reveals a eukaryotic Entner-Doudoroff glycolytic pathway. , 2012, The Plant journal : for cell and molecular biology.

[13]  F. Bux,et al.  BODIPY staining, an alternative to the Nile Red fluorescence method for the evaluation of intracellular lipids in microalgae. , 2012, Bioresource technology.

[14]  B. Simmons,et al.  Characterization of the acylglycerols and resulting biodiesel derived from vegetable oil and microalgae (Thalassiosira pseudonana and Phaeodactylum tricornutum) , 2012, Biotechnology and bioengineering.

[15]  R. Guillard,et al.  Stichochrysis immobilis is a diatom, not a chrysophyte , 1993 .

[16]  D. P. Wilson The Triradiate and other Forms of Nitzschia Closterium (Ehrenberg) Wm. Smith, Forma Minutissima of Allen and Nelson , 1946, Journal of the Marine Biological Association of the United Kingdom.

[17]  K. Gao,et al.  EFFECTS OF LOWERING TEMPERATURE DURING CULTURE ON THE PRODUCTION OF POLYUNSATURATED FATTY ACIDS IN THE MARINE DIATOM PHAEODACTYLUM TRICORNUTUM (BACILLARIOPHYCEAE) 1 , 2004 .

[18]  Q. Hu,et al.  Microwave-assisted nile red method for in vivo quantification of neutral lipids in microalgae. , 2011, Bioresource technology.

[19]  Leszek Rychlewski,et al.  The Phaeodactylum genome reveals the evolutionary history of diatom genomes , 2008, Nature.

[20]  C. Bowler,et al.  Genetic and phenotypic characterization of Phaeodactylum tricornutum (Bacillariophyceae) accessions 1 , 2007 .

[21]  M. Lapuerta,et al.  Correlation for the estimation of the cetane number of biodiesel fuels and implications on the iodine number , 2009 .

[22]  V. Smith,et al.  Differential antibacterial activities of fusiform and oval morphotypes of Phaeodactylum tricornutum (Bacillariophyceae) , 2010, Journal of the Marine Biological Association of the United Kingdom.

[23]  G. Knothe Analyzing biodiesel: standards and other methods , 2006 .

[24]  M. Posewitz,et al.  Genetic engineering of fatty acid chain length in Phaeodactylum tricornutum. , 2011, Metabolic engineering.

[25]  C. Bowler,et al.  Comparative Genomics of the Pennate Diatom Phaeodactylum tricornutum1[w] , 2005, Plant Physiology.

[26]  A. Mostaert,et al.  Enhancement of BODIPY505/515 lipid fluorescence method for applications in biofuel-directed microalgae production. , 2012, Journal of microbiological methods.

[27]  J. Sevilla,et al.  Mixotrophic growth of the microalga Phaeodactylum tricornutum: Influence of different nitrogen and organic carbon sources on productivity and biomass composition , 2005 .

[28]  Yves F Dufrêne,et al.  Nanostructure and nanomechanics of live Phaeodactylum tricornutum morphotypes. , 2008, Environmental microbiology.

[29]  P. Pribyl,et al.  Flow cytometry for the development of biotechnological processes with microalgae. , 2013, Biotechnology advances.

[30]  M. Stanley,et al.  Whole cell adhesion strength of morphotypes and isolates of Phaeodactylum tricornutum (Bacillariophyceae) , 2007 .

[31]  R. Lewin,et al.  Observations on Phaeodactylum tricornutum. , 1958, Journal of general microbiology.