Metabolic engineering of lipid catabolism increases microalgal lipid accumulation without compromising growth

• Published in: Proceedings of the National Academy of Sciences - PNAS 2013-12, Vol.110 (49), p.19748-19753
• Main Authors: Trentacoste, Emily M., Shrestha, Roshan P., Smith, Sarah R., Glé, Corine, Hartmann, Aaron C., Hildebrand, Mark, Gerwick, William H.
• Format: Article
• Language: English
• Subjects: Algae; Biofuels; Biological Sciences; Biomass; Blotting, Western; Cell growth; Chromatography, Thin Layer; Diatoms; Diatoms - genetics; Diatoms - growth & development; Diatoms - metabolism; Enzymes; Fatty acids; Flow Cytometry; Fluorescence; Gene Knockdown Techniques; Homeostasis; Light; Lipid metabolism; Lipid Metabolism - physiology; Lipids; Metabolic Engineering - methods; Metabolism; Microalgae; Microalgae - genetics; Microalgae - growth & development; Microalgae - metabolism; Organisms, Genetically Modified - genetics; Organisms, Genetically Modified - growth & development; Organisms, Genetically Modified - metabolism; Plants; RNA Interference; Silicon; Starvation; Thalassiosira pseudonana
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1309299110

Biologically derived fuels are viable alternatives to traditional fossil fuels, and microalgae are a particularly promising source, but improvements are required throughout the production process to increase productivity and reduce cost. Metabolic engineering to increase yields of biofuel-relevant lipids in these organisms without compromising growth is an important aspect of advancing economic feasibility. We report that the targeted knockdown of a multifunctional lipase/phospholipase/acyltransferase increased lipid yields without affecting growth in the diatom Thalassiosira pseudonana . Antisense-expressing knockdown strains 1A6 and 1B1 exhibited wild-type–like growth and increased lipid content under both continuous light and alternating light/dark conditions. Strains 1A6 and 1B1, respectively, contained 2.4- and 3.3-fold higher lipid content than wild-type during exponential growth, and 4.1- and 3.2-fold higher lipid content than wild-type after 40 h of silicon starvation. Analyses of fatty acids, lipid classes, and membrane stability in the transgenic strains suggest a role for this enzyme in membrane lipid turnover and lipid homeostasis. These results demonstrate that targeted metabolic manipulations can be used to increase lipid accumulation in eukaryotic microalgae without compromising growth.