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Metabolites  2013 

The Central Carbon and Energy Metabolism of Marine Diatoms

DOI: 10.3390/metabo3020325

Keywords: diatoms, Phaeodactylum tricornutum, Thalassiosira pseudonana, central carbon metabolism, photosynthesis, biofuel, lipid biosynthesis

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Abstract:

Diatoms are heterokont algae derived from a secondary symbiotic event in which a eukaryotic host cell acquired an eukaryotic red alga as plastid. The multiple endosymbiosis and horizontal gene transfer processes provide diatoms unusual opportunities for gene mixing to establish distinctive biosynthetic pathways and metabolic control structures. Diatoms are also known to have significant impact on global ecosystems as one of the most dominant phytoplankton species in the contemporary ocean. As such their metabolism and growth regulating factors have been of particular interest for many years. The publication of the genomic sequences of two independent species of diatoms and the advent of an enhanced experimental toolbox for molecular biological investigations have afforded far greater opportunities than were previously apparent for these species and re-invigorated studies regarding the central carbon metabolism of diatoms. In this review we discuss distinctive features of the central carbon metabolism of diatoms and its response to forthcoming environmental changes and recent advances facilitating the possibility of industrial use of diatoms for oil production. Although the operation and importance of several key pathways of diatom metabolism have already been demonstrated and determined, we will also highlight other potentially important pathways wherein this has yet to be achieved.

References

[1]  Hasle, G.R.; Syvertsen, E.E. Marine diatoms. In Identifying Marine Diatoms and Dinoflagellates; Elsevier: Amsterdam, The Netherland, 1996; pp. 5–385.
[2]  Villareal, T.A. Buoyancy properties of the giant diatom Ethmodiscus. J. Plankton Res. 1992, 14, 459–463, doi:10.1093/plankt/14.3.459.
[3]  Bertrand, M. Carotenoid biosynthesis in diatoms. Photosynth. Res. 2010, 106, 89–102, doi:10.1007/s11120-010-9589-x.
[4]  Kr?ger, N.; Poulsen, N. Diatoms-from cell wall biogenesis to nanotechnology. Annu. Rev. Genet. 2008, 42, 83–107, doi:10.1146/annurev.genet.41.110306.130109.
[5]  Schubert, H.; Sagert, S.; Forster, R.M. Evaluation of the different levels of variability in the underwater light field of a shallow estuary. Helgol. Mar. Res. 2001, 55, 12–22, doi:10.1007/s101520000064.
[6]  Anderson, L.W.J.; Sweeney, B.M. Diel changes in sedimentation characteristics of ditylum brightwelli: changes in cellular lipid and effects of respiratory inhibitors and ion-transport modifiers. Limnol. Oceanogr. 2007, 22, 539–552, doi:10.4319/lo.1977.22.3.0539.
[7]  Bowler, C.; Vardi, A.; Allen, A.E. Oceanographic and biogeochemical insights from diatom genomes. Annu. Rev. Mar. Sci. 2010, 2, 333–365, doi:10.1146/annurev-marine-120308-081051.
[8]  Bowler, C.; Karl, D.M.; Colwell, R.R. Microbial oceanography in a sea of opportunity. Nature 2009, 459, 180–184, doi:10.1038/nature08056.
[9]  Falkowski, P.G.; Fenchel, T.; Delong, E.F. The microbial engines that drive Earth’s biogeochemical cycles. Science 2008, 320, 1034–1039, doi:10.1126/science.1153213.
[10]  Coleman, M.L.; Sullivan, M.B.; Martiny, A.C.; Steglich, C.; Barry, K.; Delong, E.F.; Chisholm, S.W. Genomic islands and the ecology and evolution of Prochlorococcus. Science 2006, 311, 1768–1770, doi:10.1126/science.1122050.
[11]  Keeling, P.J.; Palmer, J.D. Horizontal gene transfer in eukaryotic evolution. Nat. Rev. Genet. 2008, 9, 605–618.
[12]  Curtis, B.A.; Tanifuji, G.; Burki, F.; Gruber, A.; Irimia, M.; Maruyama, S.; Arias, M.C.; Ball, S.G.; Gile, G.H.; Hirakawa, Y.; et al. Algal genomes reveal evolutionary mosaicism and the fate of nucleomorphs. Nature 2012, 492, 59–65.
[13]  Armbrust, E.V.; Berges, J.A.; Bowler, C.; Green, B.R.; Martinez, D.; Putnam, N.H.; Zhou, S.; Allen, A.E.; Apt, K.E.; Bechner, M.; et al. The genome of the diatom Thalassiosira pseudonana: ecology, evolution, and metabolism. Science 2004, 306, 79–86, doi:10.1126/science.1101156.
[14]  Bowler, C.; Allen, A.E.; Badger, J.H.; Grimwood, J.; Jabbari, K.; Kuo, A.; Maheswari, U.; Martens, C.; Maumus, F.; Otillar, R.P.; et al. The Phaeodactylum genome reveals the evolutionary history of diatom genomes. Nature 2008, 456, 239–244.
[15]  Kroth, P.G.; Chiovitti, A.; Gruber, A.; Martin-Jezequel, V.; Mock, T.; Parker, M.S.; Stanley, M.S.; Kaplan, A.; Caron, L.; Weber, T.; et al. A model for carbohydrate metabolism in the diatom Phaeodactylum tricornutum deduced from comparative whole genome analysis. PloS One 2008, 3, e1426.
[16]  Fabris, M.; Matthijs, M.; Rombauts, S.; Vyverman, W.; Goossens, A.; Baart, G.J.E. The metabolic blueprint of Phaeodactylum tricornutum reveals a eukaryotic Entner-Doudoroff glycolytic pathway. Plant. J. 2012, 70, 1004–1014.
[17]  Maheswari, U.; Jabbari, K.; Petit, J.-L.; Porcel, B.M.; Allen, A.E.; Cadoret, J.-P.; De Martino, A.; Heijde, M.; Kaas, R.; La Roche, J.; et al. Digital expression profiling of novel diatom transcripts provides insight into their biological functions. Genome Biol. 2010, 11, R85, doi:10.1186/gb-2010-11-8-r85.
[18]  Chauton, M.S.; Winge, P.; Brembu, T.; Vadstein, O.; Bones, A.M. Gene regulation of carbon fixation, storage and utilization in the diatom Phaeodactylum tricornutum acclimated to light/dark cycles. Plant. Physiol. 2012, 161, 1034–1048.
[19]  Nunn, B.L.; Aker, J.R.; Shaffer, S.A.; Tsai, S.; Strzepek, R.F.; Boyd, P.W.; Freeman, T.L.; Brittnacher, M.; Malmstr?m, L.; Goodlett, D.R. Deciphering diatom biochemical pathways via whole-cell proteomics. Aquat. Microb. Ecol. 2009, 55, 241–253, doi:10.3354/ame01284.
[20]  Hockin, N.L.; Mock, T.; Mulholland, F.; Kopriva, S.; Malin, G. The response of diatom central carbon metabolism to nitrogen starvation is different from that of green algae and higher plants. Plant. Physiol. 2012, 158, 299–312.
[21]  Murata, N.; Takahashi, S.; Nishiyama, Y.; Allakhverdiev, S.I. Photoinhibition of photosystem II under environmental stress. Biochimi. Biophys. Acta 2007, 1767, 414–421.
[22]  Goss, R.; Jakob, T. Regulation and function of xanthophyll cycle-dependent photoprotection in algae. Photosynth. Res. 2010, 106, 103–122, doi:10.1007/s11120-010-9536-x.
[23]  Lavaud, J.; Rousseau, B.; Van Gorkom, H.J.; Etienne, A.-L. Influence of the diadinoxanthin pool size on photoprotection in the marine planktonic diatom Phaeodactylum tricornutum. Plant. Physiol. 2002, 129, 1398–1406, doi:10.1104/pp.002014.
[24]  Bailleul, B.; Rogato, A.; De Martino, A.; Coesel, S.; Cardol, P.; Bowler, C.; Falciatore, A.; Finazzi, G. An atypical member of the light-harvesting complex stress-related protein family modulates diatom responses to light. Proc. Natl. Acad. Sci. USA. 2010, 107, 18214–18219, doi:10.1073/pnas.1007703107.
[25]  Domingues, N.; Matos, A.R.; Marques da Silva, J.; Cartaxana, P. Response of the diatom Phaeodactylum tricornutum to photooxidative stress resulting from high light exposure. PloS One 2012, 7, e38162.
[26]  Wu, H.; Cockshutt, A.M.; McCarthy, A.; Campbell, D.A. Distinctive photosystem II photoinactivation and protein dynamics in marine diatoms. Plant. Physiol. 2011, 156, 2184–2195, doi:10.1104/pp.111.178772.
[27]  Brunet, C.; Lavaud, J. Can the xanthophyll cycle help extract the essence of the microalgal functional response to a variable light environment? J. Plankton Res. 2010, 32, 1609–1617, doi:10.1093/plankt/fbq104.
[28]  Roberts, K.; Granum, E.; Leegood, R.C.; Raven, J.A. Carbon acquisition by diatoms. Photosynth. Res. 2007, 93, 79–88, doi:10.1007/s11120-007-9172-2.
[29]  Reinfelder, J.R. Carbon concentrating mechanisms in eukaryotic marine phytoplankton. Ann. Rev. MarI. Sci. 2011, 3, 291–315, doi:10.1146/annurev-marine-120709-142720.
[30]  Wang, Y.; Duanmu, D.; Spalding, M.H. Carbon dioxide concentrating mechanism in Chlamydomonas reinhardtii: inorganic carbon transport and CO2 recapture. Photosynth. Res. 2011, 109, 115–122, doi:10.1007/s11120-011-9643-3.
[31]  Matsuda, Y.; Nakajima, K.; Tachibana, M. Recent progresses on the genetic basis of the regulation of CO2 acquisition systems in response to CO2 concentration. Photosynth. Res. 2011, 109, 191–203, doi:10.1007/s11120-011-9623-7.
[32]  Raven, J.A. Inorganic carbon acquisition by eukaryotic algae: four current questions. Photosynth. Res. 2010, 106, 123–134, doi:10.1007/s11120-010-9563-7.
[33]  Trimborn, S.; Lundholm, N.; Thoms, S.; Richter, K.-U.; Krock, B.; Hansen, P.J.; Rost, B. Inorganic carbon acquisition in potentially toxic and non-toxic diatoms: the effect of pH-induced changes in seawater carbonate chemistry. Physiol. Plant 2008, 133, 92–105.
[34]  Martin, C.L.; Tortell, P.D. Bicarbonate transport and extracellular carbonic anhydrase in marine diatoms. Physiol. Plant 2008, 133, 106–116, doi:10.1111/j.1399-3054.2008.01054.x.
[35]  Satoh, D.; Hiraoka, Y.; Colman, B.; Matsuda, Y. Physiological and molecular biological characterization of intracellular carbonic anhydrase from the marine diatom Phaeodactylum tricornutum. Plant Physiol. 2001, 126, 1459–1470, doi:10.1104/pp.126.4.1459.
[36]  Nakajima, K.; Tanaka, A.; Matsuda, Y. SLC4 family transporters in a marine diatom directly pump bicarbonate from seawater. Proc. Natl. Acad. Sci. USA. 2013, 110, 1767–1772, doi:10.1073/pnas.1216234110.
[37]  Muto, M.; Fukuda, Y.; Nemoto, M.; Yoshino, T.; Matsunaga, T.; Tanaka, T. Establishment of a genetic transformation system for the marine pennate diatom Fistulifera sp. strain JPCC DA0580—A high triglyceride producer. Mar. Biotechnol 2013, 15, 48–55, doi:10.1007/s10126-012-9457-0.
[38]  Falciatore, A.; Casotti, R.; Leblanc, C.; Abrescia, C.; Bowler, C. Transformation of nonselectable reporter genes in marine diatoms. Mar. Biotechnol. 1999, 1, 239–251, doi:10.1007/PL00011773.
[39]  Apt, K.E.; Kroth-Pancic, P.G.; Grossman, A.R. Stable nuclear transformation of the diatom Phaeodactylum tricornutum. Mol. Gen. Genet. 1996, 252, 572–579.
[40]  Hopkinson, B.M.; Dupont, C.L.; Allen, A.E.; Morel, F.M.M. Efficiency of the CO2-concentrating mechanism of diatoms. Proc. Natl. Acad. Sci. USA. 2011, 108, 3830–3837.
[41]  Reinfelder, J.R.; Kraepiel, A.M.; Morel, F.M. Unicellular C4 photosynthesis in a marine diatom. Nature 2000, 407, 996–999, doi:10.1038/35039612.
[42]  McGinn, P.J.; Morel, F.M.M. Expression and inhibition of the carboxylating and decarboxylating enzymes in the photosynthetic C4 pathway of marine diatoms. Plant. Physiol. 2008, 146, 300–309, doi:10.1104/pp.107.110569.
[43]  Roberts, K.; Granum, E.; Leegood, R.C.; Raven, J.A. C3 and C4 pathways of photosynthetic carbon assimilation in marine diatoms are under genetic, not environmental, control. Plant Physiol. 2007, 145, 230–235, doi:10.1104/pp.107.102616.
[44]  Haimovich-Dayan, M.; Garfinkel, N.; Ewe, D.; Marcus, Y.; Gruber, A.; Wagner, H.; Kroth, P.G.; Kaplan, A. The role of C4 metabolism in the marine diatom Phaeodactylum tricornutum. New Phytol. 2013, 197, 177–185, doi:10.1111/j.1469-8137.2012.04375.x.
[45]  Wilhelm, C.; Büchel, C.; Fisahn, J.; Goss, R.; Jakob, T.; Laroche, J.; Lavaud, J.; Lohr, M.; Riebesell, U.; Stehfest, K.; et al. The regulation of carbon and nutrient assimilation in diatoms is significantly different from green algae. Protist 2006, 157, 91–124, doi:10.1016/j.protis.2006.02.003.
[46]  Shimonaga, T.; Konishi, M.; Oyama, Y.; Fujiwara, S.; Satoh, A.; Fujita, N.; Colleoni, C.; Buléon, A.; Putaux, J.-L.; Ball, S.G.; et al. Variation in storage alpha-glucans of the Porphyridiales (Rhodophyta). Plant Cell. Physiol. 2008, 49, 103–116, doi:10.1093/pcp/pcm172.
[47]  Granum, E.; Kirkvold, S.; Myklestad, S. Cellular and extracellular production of carbohydrates and amino acids by the marine diatom Skeletonema costatum: diel variations and effects of N depletion. Mar. Ecol. Prog. Ser. 2002, 242, 83–94, doi:10.3354/meps242083.
[48]  Roessler, P.G. UDP-glucose pyrophosphorylase activity in the diatom Cyclotella cryptica. Pathways of chrysolaminarin biosynthesis. J. Phycol. 1987, 23, 494–498, doi:10.1111/j.1529-8817.1987.tb02536.x.
[49]  V?rum, K.M.; ?stgaard, K.; Grimsrud, K. Diurnal rhythms in carbohydrate metabolism of the marine diatom Skeletonema costatum (Grev.) Cleve. J. Exp. Mar. Bio. Ecol. 1986, 102, 249–256, doi:10.1016/0022-0981(86)90180-2.
[50]  Parker, M.S.; Armbrust, E.V.; Piovia-Scott, J.; Keil, R.G. Induction of photorespiration by light in the centric diatom Thalassiosira weissflogii (Bacillariophyceae): Molecular characterization and physiological consequences. J. Phycol. 2004, 40, 557–567, doi:10.1111/j.1529-8817.2004.03184.x.
[51]  Timm, S.; Nunes-Nesi, A.; P?rnik, T.; Morgenthal, K.; Wienkoop, S.; Keerberg, O.; Weckwerth, W.; Kleczkowski, L.A.; Fernie, A.R.; Bauwe, H. A cytosolic pathway for the conversion of hydroxypyruvate to glycerate during photorespiration in Arabidopsis. Plant. Cell. 2008, 20, 2848–2859, doi:10.1105/tpc.108.062265.
[52]  Tortell, P.D. Evolutionary and ecological perspectives on carbon acquisition in phytoplankton. Limonol. Oceanogr. 2000, 45, 744–750.
[53]  Fernie, A.R.; Obata, T.; Allen, A.E.; Araújo, W.L.; Bowler, C. Leveraging metabolomics for functional investigations in sequenced marine diatoms. Trends Plant. Sci. 2012, 17, 395–403.
[54]  Allen, A.E.; Dupont, C.L.; Oborník, M.; Horák, A.; Nunes-Nesi, A.; McCrow, J.P.; Zheng, H.; Johnson, D.A.; Hu, H.; Fernie, A.R.; et al. Evolution and metabolic significance of the urea cycle in photosynthetic diatoms. Nature 2011, 473, 203–207.
[55]  Martinez, E.; Antoine, D.; D’Ortenzio, F.; Gentili, B. Climate-driven basin-scale decadal oscillations of oceanic phytoplankton. Science 2009, 326, 1253–1256.
[56]  Weber, T.; Deutsch, C. Oceanic nitrogen reservoir regulated by plankton diversity and ocean circulation. Nature 2012, 489, 419–422, doi:10.1038/nature11357.
[57]  Weber, T.S.; Deutsch, C. Ocean nutrient ratios governed by plankton biogeography. Nature 2010, 467, 550–554, doi:10.1038/nature09403.
[58]  Intergovernmental Panel on Climate Change (IPCC). Climate Change 2001; Houghton, J.T., Ding, Y., Griggs, D.J., Noguer, M., van der Linden, P.J., Dai, X., Maskell, K., Johnson, C.A., Eds.; Oxford University Press: Oxford, UK, 2001.
[59]  Field, C.B. Primary Production of the Biosphere: Integrating Terrestrial and Oceanic Components. Science 1998, 281, 237–240.
[60]  Hein, M.; Sand-Jensen, K. CO2 increases oceanic primary production. 1997, 388, 526–527.
[61]  Yang, G.; Gao, K. Physiological responses of the marine diatom Thalassiosira pseudonana to increased pCO2 and seawater acidity. Mar. Environ. Res. 2012, 79, 142–151.
[62]  Gao, K.; Xu, J.; Gao, G.; Li, Y.; Hutchins, D.A.; Huang, B.; Wang, L.; Zheng, Y.; Jin, P.; Cai, X.; et al. Rising CO2 and increased light exposure synergistically reduce marine primary productivity. Nat. Clim. Change 2012, 2, 519–523.
[63]  Crawfurd, K.J.; Raven, J.A.; Wheeler, G.L.; Baxter, E.J.; Joint, I. The response of Thalassiosira pseudonana to long-term exposure to increased CO2 and decreased pH. PloS one 2011, 6, e26695.
[64]  Boyd, P.W.; Watson, A.J.; Law, C.S.; Abraham, E.R.; Trull, T.; Murdoch, R.; Bakker, D.C.; Bowie, A.R.; Buesseler, K.O.; Chang, H.; et al. A mesoscale phytoplankton bloom in the polar Southern Ocean stimulated by iron fertilization. Nature 2000, 407, 695–702.
[65]  Coale, K.H.; Johnson, K.S.; Chavez, F.P.; Buesseler, K.O.; Barber, R.T.; Brzezinski, M.A.; Cochlan, W.P.; Millero, F.J.; Falkowski, P.G.; Bauer, J.E.; et al. Southern Ocean iron enrichment experiment: carbon cycling in high- and low-Si waters. Science 2004, 304, 408–414.
[66]  Boyd, P.W.; Jickells, T.; Law, C.S.; Blain, S.; Boyle, E.A.; Buesseler, K.O.; Coale, K.H.; Cullen, J.J.; De Baar, H.J.W.; Follows, M.; et al. Mesoscale iron enrichment experiments 1993–2005: synthesis and future directions. Science 2007, 315, 612–617.
[67]  Cao, L.; Caldeira, K. Can ocean iron fertilization mitigate ocean acidification? Clim. Change 2010, 99, 303–311.
[68]  Strzepek, R.F.; Harrison, P.J. Photosynthetic architecture differs in coastal and oceanic diatoms. Nature 2004, 431, 689–692.
[69]  Peers, G.; Price, N.M. Copper-containing plastocyanin used for electron transport by an oceanic diatom. Nature 2006, 441, 341–344.
[70]  Kustka, A.B.; Allen, A.E.; Morel, F.M.M. Sequence analysis and transcriptional regulation of iron acquisition genes in two marine diatoms. J. Phycol. 2007, 43, 715–729.
[71]  Allen, A.E.; Laroche, J.; Maheswari, U.; Lommer, M.; Schauer, N.; Lopez, P.J.; Finazzi, G.; Fernie, A.R.; Bowler, C. Whole-cell response of the pennate diatom Phaeodactylum tricornutum to iron starvation. Proc. Natl. Acad. Sci. USA 2008, 105, 10438–10443.
[72]  Schirmer, K.; Fischer, B.B.; Madureira, D.J.; Pillai, S. Transcriptomics in ecotoxicology. Anal. Bioanal. Chem. 2010, 397, 917–923.
[73]  Diggs, D.L.; Huderson, A.C.; Harris, K.L.; Myers, J.N.; Banks, L.D.; Rekhadevi, P. V.; Niaz, M.S.; Ramesh, A. Polycyclic aromatic hydrocarbons and digestive tract cancers: a perspective. J. Environ. Sci. Heal. C 2011, 29, 324–357.
[74]  Tobiszewski, M.; Namie?nik, J. PAH diagnostic ratios for the identification of pollution emission sources. Environ. Pollut. 2012, 162, 110–119.
[75]  Carvalho, R.N.; Bopp, S.K.; Lettieri, T. Transcriptomics responses in marine diatom Thalassiosira pseudonana exposed to the polycyclic aromatic hydrocarbon benzo[a]pyrene. PloS One 2011, 6, e26985.
[76]  Becker, E.W. Microalgae: Biotechnology and Microbiology; Cambridge University Press: Cambridge, UK, 1994; p. 293.
[77]  Lee, Y.K. Microalgal mass culture systems and methods: Their limitation and potential. J. Appl. Phycol. 2001, 13, 307–315.
[78]  Pulz, O.; Gross, W. Valuable products from biotechnology of microalgae. Appl. Microbiol. Biotechnol. 2004, 65, 635–648.
[79]  Harun, R.; Singh, M.; Forde, G.M.; Danquah, M.K. Bioprocess engineering of microalgae to produce a variety of consumer products. Renew. Sust. Energ. Rev. 2010, 14, 1037–1047.
[80]  Chisti, Y. Biodiesel from microalgae. Biotechnol. Adv. 2007, 25, 294–306.
[81]  Schenk, P.M.; Thomas-Hall, S.R.; Stephens, E.; Marx, U.C.; Mussgnug, J.H.; Posten, C.; Kruse, O.; Hankamer, B. Second generation biofuels: High-efficiency microalgae for biodiesel production. Bioenerg. Res. 2008, 1, 20–43.
[82]  Sheehan, J.; Dunahay, T.; Benemann, J.; Roessler, P. Look Back at the U.S. Department of Energy’s Aquatic Species Program: Biodiesel from Algae. Close-Out Report. NREL/TP-580-24190, 1998.
[83]  Hu, Q.; Sommerfeld, M.; Jarvis, E.; Ghirardi, M.; Posewitz, M.; Seibert, M.; Darzins, A. Microalgal triacylglycerols as feedstocks for biofuel production: perspectives and advances. Plant J. 2008, 54, 621–639.
[84]  Spolaore, P.; Joannis-Cassan, C.; Duran, E.; Isambert, A. Commercial applications of microalgae. J. Biosci. Bioeng. 2006, 101, 87–96.
[85]  Khozin-Goldberg, I.; Cohen, Z. Unraveling algal lipid metabolism: Recent advances in gene identification. Biochimie 2011, 93, 91–100.
[86]  Wijffels, R.H.; Barbosa, M.J. An outlook on microalgal biofuels. Science 2010, 329, 796–799.
[87]  Caldana, C.; Li, Y.; Leisse, A.; Zhang, Y.; Bartholomaeus, L.; Fernie, A.R.; Willmitzer, L.; Giavalisco, P. Systemic analysis of inducible target of rapamycin mutants reveal a general metabolic switch controlling growth in Arabidopsis thaliana. Plant J. 2013, doi:10.1111/tpj.12080.
[88]  Scott, S.A.; Davey, M.P.; Dennis, J.S.; Horst, I.; Howe, C.J.; Lea-Smith, D.J.; Smith, A.G. Biodiesel from algae: challenges and prospects. Curr. Opin. Biotechnol. 2010, 21, 277–286.
[89]  Derelle, E.; Ferraz, C.; Rombauts, S.; Rouzé, P.; Worden, A.Z.; Robbens, S.; Partensky, F.; Degroeve, S.; Echeynié, S.; Cooke, R.; et al. Genome analysis of the smallest free-living eukaryote Ostreococcus tauri unveils many unique features. Proc. Natl. Acad. Sci. USA 2006, 103, 11647–11652.
[90]  Merchant, S.S.; Prochnik, S.E.; Vallon, O.; Harris, E.H.; Karpowicz, S.J.; Witman, G.B.; Terry, A.; Salamov, A.; Fritz-Laylin, L.K.; Maréchal-Drouard, L.; et al. The Chlamydomonas genome reveals the evolution of key animal and plant functions. Science 2007, 318, 245–250.
[91]  Price, D.C.; Chan, C.X.; Yoon, H.S.; Yang, E.C.; Qiu, H.; Weber, A.P.M.; Schwacke, R.; Gross, J.; Blouin, N.A.; Lane, C.; et al. Cyanophora paradoxa genome elucidates origin of photosynthesis in algae and plants. Science 2012, 335, 843–847.
[92]  Tirichine, L.; Bowler, C. Decoding algal genomes: tracing back the history of photosynthetic life on Earth. Plant J. 2011, 66, 45–57.
[93]  Gong, Y.; Zhang, J.; Guo, X.; Wan, X.; Liang, Z.; Hu, C.J.; Jiang, M. Identification and characterization of PtDGAT2B, an acyltransferase of the DGAT2 acyl-coenzyme A: diacylglycerol acyltransferase family in the diatom Phaeodactylum tricornutum. FEBS Lett. 2013, 587, 481–487.
[94]  Guihéneuf, F.; Leu, S.; Zarka, A.; Khozin-Goldberg, I.; Khalilov, I.; Boussiba, S. Cloning and molecular characterization of a novel acyl-CoA:diacylglycerol acyltransferase 1-like gene (PtDGAT1) from the diatom Phaeodactylum tricornutum. FEBS J. 2011, 278, 3651–3666.
[95]  Merchant, S.S.; Kropat, J.; Liu, B.; Shaw, J.; Warakanont, J. TAG, you’re it! Chlamydomonas as a reference organism for understanding algal triacylglycerol accumulation. Curr. Opin. Biotechnol. 2012, 23, 352–363.
[96]  Riekhof, W.R.; Sears, B.B.; Benning, C. Annotation of genes involved in glycerolipid biosynthesis in Chlamydomonas reinhardtii: discovery of the betaine lipid synthase BTA1Cr. Eukaryot. Cell 2005, 4, 242–252.
[97]  Liu, B.; Benning, C. Lipid metabolism in microalgae distinguishes itself. Curr. Opin. Biotechnol. 2012, doi:10.1016/j.copbio.2012.08.008.
[98]  Borowitzka, M.A. Fats, oils and hydrocarbons. In Microalgal biotechnology; Borowitzka, M.A., Borowitzka, L.J., Eds.; Cambridge University Press: Cambridge, UK, 1988; pp. 257–287.
[99]  Dunstan, G.A.; Volkman, J.K.; Barrett, S.M.; Leroi, J.-M.; Jeffrey, S.W. Essential polyunsaturated fatty acids from 14 species of diatom (Bacillariophyceae). Phytochemistry 1993, 35, 155–161.
[100]  Yu, E.T.; Zendejas, F.J.; Lane, P.D.; Gaucher, S.; Simmons, B.A.; Lane, T.W. Triacylglycerol accumulation and profiling in the model diatoms Thalassiosira pseudonana and Phaeodactylum tricornutum (Baccilariophyceae) during starvation. J. Appl. Phycol. 2009, 21, 669–681.
[101]  Rezanka, T.; Lukavsky, J.; Nedbalová, L.; Kolouchová, I.; Sigler, K. Effect of starvation on the distribution of positional isomers and enantiomers of triacylglycerol in the diatom Phaeodactylum tricornutum. Phytochemistry 2012, 80, 17–27.
[102]  Wang, Z.T.; Ullrich, N.; Joo, S.; Waffenschmidt, S.; Goodenough, U. Algal lipid bodies: stress induction, purification, and biochemical characterization in wild-type and starchless Chlamydomonas reinhardtii. Eukaryot. Cell. 2009, 8, 1856–1868.
[103]  Moellering, E.R.; Benning, C. RNA interference silencing of a major lipid droplet protein affects lipid droplet size in Chlamydomonas reinhardtii. Eukaryot. Cell 2010, 9, 97–106.
[104]  Miller, R.; Wu, G.; Deshpande, R.R.; Vieler, A.; G?rtner, K.; Li, X.; Moellering, E.R.; Z?uner, S.; Cornish, A.J.; Liu, B.; et al. Changes in transcript abundance in Chlamydomonas reinhardtii following nitrogen deprivation predict diversion of metabolism. Plant. Physiol. 2010, 154, 1737–1752.
[105]  Mock, T.; Samanta, M.P.; Iverson, V.; Berthiaume, C.; Robison, M.; Holtermann, K.; Durkin, C.; Bondurant, S.S.; Richmond, K.; Rodesch, M.; et al. Whole-genome expression profiling of the marine diatom Thalassiosira pseudonana identifies genes involved in silicon bioprocesses. Proc. Natl. Acad. Sci. USA. 2008, 105, 1579–1584.
[106]  Stehfest, K.; Toepel, J.; Wilhelm, C. The application of micro-FTIR spectroscopy to analyze nutrient stress-related changes in biomass composition of phytoplankton algae. Plant Physiol. Biochem. 2005, 43, 717–726.
[107]  Quigg, A.; Beardall, J. Protein turnover in relation to maintenance metabolism at low photon flux in two marine microalgae. Plant. Cell. Environ. 2003, 26, 693–703.
[108]  Jiang, Y.; Yoshida, T.; Quigg, A. Photosynthetic performance, lipid production and biomass composition in response to nitrogen limitation in marine microalgae. Plant. Physiol. Biochem. 2012, 54, 70–77.
[109]  Lombardi, A.; Wangersky, P. Influence of phosphorus and silicon on lipid class production by the marine diatom Chaetoceros gracilis grown in turbidostat cage cultures. Mar. Ecol. Prog. Ser. 1991, 77, 39–47.
[110]  McGinnis, K.M.; Dempster, T.A.; Sommerfeld, M.R. Characterization of the growth and lipid content of the diatom Chaetoceros muelleri. J. Appl. Phycol. 1997, 9, 19–24.
[111]  Roessler, P.G. Changes in the activities of various lipid and carbohydrate biosynthetic enzymes in the diatom Cyclotella cryptica in response to silicon deficiency. Arch. Biochem. Biophys. 1988, 267, 521–528.
[112]  Huang, A.; He, L.; Wang, G. Identification and characterization of microRNAs from Phaeodactylum tricornutum by high-throughput sequencing and bioinformatics analysis. BMC Genomics 2011, 12, 337.
[113]  Reitan, K.I.; Rainuzzo, J.R.; Olsen, Y. Effect of nutrient limitation of fatty acid and lipid content of marine microalgae. J. Phycol. 1994, 30, 972–979.
[114]  Van Mooy, B.A.S.; Fredricks, H.F.; Pedler, B.E.; Dyhrman, S.T.; Karl, D.M.; Koblízek, M.; Lomas, M.W.; Mincer, T.J.; Moore, L.R.; Moutin, T.; et al. Phytoplankton in the ocean use non-phosphorus lipids in response to phosphorus scarcity. Nature 2009, 458, 69–72.
[115]  Martin, P.; Van Mooy, B.A.S.; Heithoff, A.; Dyhrman, S.T. Phosphorus supply drives rapid turnover of membrane phospholipids in the diatom Thalassiosira pseudonana. ISME J. 2011, 5, 1057–1060.
[116]  Dyhrman, S.T.; Jenkins, B.D.; Rynearson, T.A.; Saito, M.A.; Mercier, M.L.; Alexander, H.; Whitney, L.P.; Drzewianowski, A.; Bulygin, V.V; Bertrand, E.M.; et al. The transcriptome and proteome of the diatom Thalassiosira pseudonana reveal a diverse phosphorus stress response. PloS One 2012, 7, e33768.
[117]  Alonso, D.L.; Belarbi, E.H.; Fernández-Sevilla, J.M.; Rodríguez-Ruiz, J.; Molina Grima, E. Acyl lipid composition variation related to culture age and nitrogen concentration in continuous culture of the microalga Phaeodactylum tricornutum. Phytochemistry 2000, 54, 461–471.
[118]  Liang, Y.; Beardall, J.; Heraud, P. Changes in growth, chlorophyll fluorescence and fatty acid composition with culture age in batch cultures of Phaeodactylum tricornutum and Chaetoceros muelleri (Bacillariophyceae). Bot. Mar. 2006, 49, 165–173.

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