Journals / Turkish Journal of Botany / 2019 / Cilt: 43 - Sayı: 4

Two pronounced Chlorella strains for efficient biodiesel feedstock production

Pages
458–467
Publication Date
2022-11-04
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

IMU17 might stand as a promising candidate for biodiesel feedstock production with its low PUFA content and aconcomitant induction of saturation of fatty acids as a clear response to N-deprivation.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:In this study, two indigenous Chlorella strains were evaluated for triacylglycerol (TAG) production and related parametersduring 10 days of N-deprivation.
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Key Findings & Data:IMU12 and Chlorella sp.
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Conclusion & Impact:IMU17 might stand as a promising candidate for biodiesel feedstock production with its low PUFA content and aconcomitant induction of saturation of fatty acids as a clear response to N-deprivation.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

In this study, two indigenous Chlorella strains were evaluated for triacylglycerol (TAG) production and related parametersduring 10 days of N-deprivation. The strains were identified based on morphological characteristics and genomic information, namedas Chlorella sp. IMU12 and Chlorella sp. IMU17. Time-dependent reduction of growth was accompanied by decreased chlorophyllcontent, reduced oxygen evolution ratio, and elevated carotenoid content of both strains cultivated in N-free Bold’s basal medium.Nitrogen deprivation induced total lipid and neutral lipid content in both strains, supported by FTIR measurement of TAGs. Chlorellasp. IMU17 showed higher production of TAGs as a response to N-deprivation. Strikingly, relative polysaccharide content showed arapid increase on the first days and a noticeable reduction was recorded especially after 5 days of N-deprivation while TAG productionshowed a gradual increase during the whole period of N-deprivation in both strains. Starch might be a predominant form of carbonstorage in the short term and the continuous increase of TAG production might be supported by degradation of starch in a longerperiod of N-deprivation. FAME analysis of lipids showed that the saturation level of the fatty acids of both strains meets the Europeanstandard EN 14214 requirements. Lastly, N-deprivation stimulated a significant reduction of PUFA production in Chlorella sp. IMU17.Thus, Chlorella sp. IMU17 might stand as a promising candidate for biodiesel feedstock production with its low PUFA content and aconcomitant induction of saturation of fatty acids as a clear response to N-deprivation.

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Cite This Article

ÇAKMAK, T., TÜZÜN, İ., ÇAKMAK, Z. E., YOUNG, E. (2022). Two pronounced Chlorella strains for efficient biodiesel feedstock production. Turkish Journal of Botany, Cilt: 43 - Sayı: 4, 458–467. https://ajindex.com/articles/600894

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References (13)

  1. Berges JA, Charwbois DO, Mauzerali DC, Falkowski PG (1996). Differential effects of nitrogen limitation on photosynthetic efficiency of photosystems I and II in microalgae. Plant Physiology 110: 689-696.
  2. Bligh E, Dyer W (1959). A rapid method for total lipid extraction and purification. Canadian Journal of Bıochemistry and Physiology 37: 911-917.
  3. Borowitzka MA, Borowitzka LJ (1988) Dunaliella. In: Borowitzka MA (editors) Micro-algal Biotechnology. Cambridge, UK: Cambridge University Press, pp. 27-58.
  4. Cagliari A, Margis R, Maraschin FS, Turchetto Zolet AC, Loss G et al. (2011). Biosynthesis of triacylglycerols (TAGs) in plants and algae. International Journal of Plant Biology 2: 40-52.
  5. Chisti Y (2008). Biodiesel from microalgae beats bioethanol. Trends in Biotechnology 26: 126-131.
  6. Dean A, Sigee D, Estrada B, Pittman J (2010). Using FTIR spectroscopy for rapid determination of lipid accumulation in response to nitrogen limitation in freshwater microalgae. Bioresource Technology 101: 4499-4507.
  7. Elibol Cakmak Z, Olmez TT, Cakmak T, Menemen Y, Tekinay T (2014). Induction of triacylglycerol production in Chlamydomonas reinhardtii: comparative analysis of different element regimes. Bioresource Technology 155: 379-387.
  8. Elsey D, Jameson D, Raleigh B, Cooney MJ (2007). Fluorescent measurement of microalgal neutral lipids. Journal of Microbiological Methods 68: 639-642.
  9. Francisco E, Neves D, Jacob-Lopes E, Franco T (2010). Microalgae as feedstock for biodiesel production: carbon dioxide sequestration, lipid production and biofuel quality. Journal of Chemical Technology and Biotechnology 85: 395-403.
  10. Gors M, Schumann R, Hepperle D, Karsten U (2010). Quality analysis of commercial Chlorella products used as dietary supplement in human nutrition. Journal of Applied Phycology 22: 265-276.
  11. Grima EM, Belarbi EH, Fernandez FGA, Medina AR, Chisti Y (2003). Recovery of microalgal biomass and metabolites: process options and economics. Biotechnology Advances 20: 491-515.
  12. Guarnieri MT, Nag A, Smolinski SL, Darzins A, Seibert M et al. (2011). Examination of triacylglycerol biosynthetic pathways via de novo transcriptomic and proteomic analyses in an unsequenced microalga. PLoS One 6 (10): e25851. Hoham R, Bonome T, Martin C, Leebens-Mack J (2002). A combined 18S rDNA and rbcL phylogenetic analysis of Chloromonas and Chlamydomonas (Chlorophyceae, Volvocales) emphasizing snow and other cold-temperature habitats. Journal of Phycology 38: 1051-1064.
  13. Huang GH, Chen F, Wei D, Zhang X