Energy innovation potential of oleaginous microalgae

• Wijffels RH, Barbosa MJ. An outlook on microalgal biofuels. Science329(5993),796–799 (2010).
   PubMed Web of Science ®Google Scholar
• Bosak T, Liang B, Sim MS, Petroff AP. Morphological record of oxygenic photosynthesis in conical stromatolites. Proc. Natl Acad. Sci. USA106(27),10939–10943 (2009).
   PubMed Web of Science ®Google Scholar
• Kump LR. The rise of atmospheric oxygen. Nature451(7176),277–278 (2008).
   PubMed Web of Science ®Google Scholar
• Payne JL, Boyer AG, Brown JH et al. Two-phase increase in the maximum size of life over 3.5 billion years reflects biological innovation and environmental opportunity. Proc. Natl Acad. Sci. USA106(1),24–27 (2009).
   PubMed Web of Science ®Google Scholar
• Stasiuk LD. Confocal laser scanning fluorescence microscopy of Botryococcus alginite from boghead oil shale, Boltysk, Ukraine: selective preservation of various micro-algal components. Org. Geochem.30,1021–1026 (1999).
   Web of Science ®Google Scholar
• Chisti Y. Biodiesel from microalgae. Biotech. Adv.25(3),294–306 (2007).
   PubMed Web of Science ®Google Scholar
• Chisti Y. Fuels from microalgae. Biofuels1(2),233–235 (2010).
   Google Scholar
• Vijayaragh K, Karthik R, Kamala Nalini SP. Hydrogen generation from algae: a review. J. Plant. Sci.5(1),1–19 (2010).
   Google Scholar
• Yen H-W, Brune DE. Anaerobic co-digestion of algal sludge and waste paper to produce methane. Bioresour. Technol.98(1),130–134 (2007).
   PubMed Web of Science ®Google Scholar
• Sheehan J, Dunahay TG, Benemann JR, Roessler PG, Weissman JC. A Look Back at the US Department of Energy’s Aquatic Species Program: Biodiesel from Algae. National Renewable Energy Laboratory, Golden, CO, USA (1998).
   Google Scholar
• Haag AL. Algae bloom again. Nature447(31),520–521 (2007).
   PubMed Web of Science ®Google Scholar
• Wada H, Murata N. The essential role of phosphatidylglycerol in photosynthesis. Photosynth. Res.92(2),205–215 (2007).
   PubMed Web of Science ®Google Scholar
• Atadashi IM, Aroua MK, Abdul-Aziz A. High quality biodiesel and its diesel engine application. Renew Sustain Energ Rev.14(7),1999–2008 (2010).
   Web of Science ®Google Scholar
• Aatola H, Larmi M, Sarjovaara T, Mikkonen S. Hydrotreatedd vegetable oil (HVO) as a renewable diesel fuel: trade-off between NOx particulate emission and fuel consumption of a heavy duty engine. SAE Int. J. Engines1,1251–1262 (2008).
   Google Scholar
• Fishman D, Majumdar R, Morello J, Pate R, Yang J. National Algal Biofuels Technology Roadmap. US Department of Energy, Office of Energy Efficiency and Renewable Energy, Biomass Program, Washington, DC, USA (2010).
   Google Scholar
• Rezanka T, Zahradník J, Podojil M. Hydrocarbons in green and blue-green algae. Folia Microbiologica27(6),450–454 (1982).
   PubMed Web of Science ®Google Scholar
• Metzger P, Largeau C. Botryococcus braunii: a rich source for hydrocarbons and related ether lipids. Appl. Microbiol. Biotechnol.66(5),486–496 (2005).
   PubMed Web of Science ®Google Scholar
• Kawachi M, Tanoi T, Demura M, Kaya K, Watanabe MM. Relationship between hydrocarbons and molecular phylogeny of Botryococcus braunii. Algal Res. doi:10.1016/j.algal.05.003 (2012) (In press).
   Google Scholar
• Niehaus TD, Okada S, Devarenne TP et al. Identification of unique mechanisms for triterpene biosynthesis in Botryococcus braunii. Proc. Natl Acad. Sci. USA108(30),12260–12265 (2011).
   PubMed Web of Science ®Google Scholar
• Nagano S, Yamamoto S, Nagakubo M, Atsumi K, Watanabe MM. Physical properties of hydrocarbon oils produced by Botryococcus braunii with special reference to the density, kinematic viscosity, surface tension, and distillation properties. Procedia Environ. Sci.15,73–79 (2012).
   Google Scholar
• Peyronel D, Artaud J, Iatrides MC, Rancurel P, Chevalier JL. Fatty acid and squalene compositions of Mediterranean Centrophorus SPP egg and liver oils in relation to age. Lipids19(9),643–648 (1984).
   PubMed Web of Science ®Google Scholar
• Chang M-H, Kim H-J, Jahng K-Y, Hong S-C. The isolation and characterization of Pseudozyma sp. JCC 207, a novel producer of squalene. Appl. Microbiol. Biotechnol.78(6),963–972 (2008).
   PubMed Web of Science ®Google Scholar
• Kimura T. Liu C. Li X. Maekawa T. Asaoka S. Conversion of isoprenoid oil by catalytic cracking and hydrocracking over nanoporous hybrid catalysts. J. Biomed. Biotechnol.637125 (2012).
   PubMedGoogle Scholar
• Chaiwong K, Kiatsiriroat T, Vorayos N, Thararax C. Biochar production from freshwater algae by slow pyrolysis. J. Sci. Technol.6(2),186–195 (2012).
   Google Scholar
• Demura M, Kawachi M, Koshikawa H, Nakayama T, Mayuzumi Y, Watanabe MM. Succession of genetic diversity of Botryococcus braunii (Trebouxiophyceae) in two Japanese reservoirs. Procedia Environ. Sci.1(5),3–11 (2012).
   Google Scholar
• Watanabe MM, Tanabe Y. Biology and industrial potential of Botryococcus braunii. In: Handbook of Microalgal Culture (2nd Edition). Wiley-Blackwell, Oxford, UK (2012) (In press).
   Google Scholar
• Ge Y, Lu J, Tian G. Growth characteristics of Botryococcus braunii 765 under high CO2 concentration in photobioreactor. Bioresour. Technol.102,130–134 (2011).
   PubMed Web of Science ®Google Scholar
• Tanoi T, Kawachi M, Watanabe MM. Effects of carbon source on growth and morphology of Botryococcus braunii. J. Appl. Phycol.23(1),25–33 (2011).
   Web of Science ®Google Scholar
• Ioki M, Baba M, Bidadi H et al. Modes of hydrocarbon oil biosynthesis revealed by comparative gene expression analysis for race A and race B strains of Botryococcus braunii. Bioresour. Technol.109,271–276 (2012).
   PubMed Web of Science ®Google Scholar
• Yokoyama R, Honda D. Taxonomic rearrangement of the genus Schizochytrium sensu lato based on morphology, chemotaxonomic characteristics, and 18S rRNA gene phylogeny (Thraustochytriaceae, Labyrinthulomycetes): emendation for Schizochytrium and erection of Aurantiochytrium and Oblongichytrium gen. nov. Mycoscience48(4),199–211 (2007).
   Google Scholar
• Honda D, Yokochi T, Nakahara T, Erata M, Higashihara T. Schizochytrium limacinum sp. nov., a new thraustochytrid from a mangrove area in the west Pacific Ocean. Mycol. Res.102(4),439–448 (1998).
   Web of Science ®Google Scholar
• Raghu-Kumar S. Schizochytrium mangrovei sp. nov., a thraustochytrid from mangroves in India. Transact. British Mycol. Soc.90(4),627–631 (1988).
   Google Scholar
• Rosa SM, Soria MA, Vélez CG, Galvagno MA. Improvement of a two-stage fermentation process for docosahexaenoic acid production by Aurantiochytrium limacinum SR21 applying statistical experimental designs and data analysis. Bioresour. Technol.101(7),2367–2374 (2010).
   PubMed Web of Science ®Google Scholar
• Liang Y, Sarkany N, Cui Y et al. Use of sweet sorghum juice for lipid production by Schizochytrium limacinum SR21. Bioresour. Technol.101(10),3623–3627 (2010).
   PubMed Web of Science ®Google Scholar
• Chen G, Fan KW, Lu FP et al. Optimization of nitrogen source for enhanced production of squalene from thraustochytrid Aurantiochytrium sp. New Biotechnol.27(4),382–389 (2010).
   PubMed Web of Science ®Google Scholar
• Kaya K, Nakazawa A, Matsuura H et al. Thraustochytrid Aurantiochytrium sp. 18W-13a accumulates high amounts of squalene. Biosci. Biotechnol. Biochem.75(11),2246–2248 (2011).
   PubMed Web of Science ®Google Scholar
• Nakazawa A, Matsuura H, Kose R et al. Optimization of culture conditions of the thraustochytrid Aurantiochytrium sp. strain 18W-13a for squalene production. Bioresour. Technol.109,287–291 (2012).
   PubMed Web of Science ®Google Scholar
• Oswald WJ, Gotaas HB. Golueke CG, Kellen WR, Gloyna EF, Hermann ER. Algae in waste treatment. Sewage Ind. Wastes29,437–457 (1957).
   Google Scholar
• Pittman JK. Dean AP, Osundeko O. The potential of sustainable algal biofuel production using wastewater resources. Bioresour Technol.102,17–25 (2011).
   PubMed Web of Science ®Google Scholar
• Lam MK, Lee KT. Microalgae biofuels: a critical review of issues, problems and the way forward. Biotechnol. Adv.30,673–690 (2012).
   PubMed Web of Science ®Google Scholar
• Canakci M. Sanli H. Biodiesel production from various feedstocks and their effects on the fuel properties. J. Ind. Microbiol. Biotechnol.35,431–441 (2008).
   PubMed Web of Science ®Google Scholar
• Xiong W, Li XF, Xiang JY, Wu QY. High-density fermentation of microalga Chlorella protothecoides in bioreactor for microbio-diesel production. Appl. Microbiol. Biotechnol.78,29–36 (2008).
   PubMed Web of Science ®Google Scholar
• Clarens AF, Resurreccion EP, White MA, Colosi LM. Environmental life cycle comparison of algae to other bioenergy feedstocks. Environ. Sci. Technol.44,1813–1819 (2010).
   PubMed Web of Science ®Google Scholar
• Yonezawa N, Matsuura H, Shiho M, Kaya K, Watanabe MM. Effects of soybean curd wastewater on the growth and hydrocarbon production of Botryococcus braunii strain BOT-22. Bioresour Technol.109,304–307 (2012).
   PubMed Web of Science ®Google Scholar
• Ioki M, Ohkoshi M, Nakahira-Yanaka Y, Nakajima N, Watanabe MM. Isolation of herbicide-resistant mutants of Botryococcus braunii. Bioresour. Technol.109,300–303 (2012).
   PubMed Web of Science ®Google Scholar
• Li Y, Zhou W, Hu B, Min M, Chen P, Ruan RR. Integration of algae cultivation as biodiesel production feedstock with municipal wastewater treatment: strains screening and significance evaluation of environmental factors. Bioresour. Technol.102,10861–10867 (2011).
   PubMed Web of Science ®Google Scholar
• Órpez R, Martínez ME, Hodaifa G, Yousfi FE, Jbari N, Sánchez S. Growth of the microalga Botryococcus braunii in secondarily treated sewage. Desalination246,625–630 (2009).
   Web of Science ®Google Scholar
• Zhou W, Li Y, Min M, Hu B, Chen P, Ruan R. Local bioprospecting for high-lipid producing microalgal strains to be grown on concentrated municipal wastewater for biofuel production. Bioresour. Technol.102,6909–6919 (2011).
   PubMed Web of Science ®Google Scholar
• Sydney EB, da Silva TE, Tokarski A et al. Screening of microalgae with potential for biodiesel production and nutrient removal from treated domestic sewage. Appl. Energy88,3291–3294 (2011).
   Web of Science ®Google Scholar
• Zhou W, Min M, Li Y et al. A hetero-photoautotrophic two-stage cultivation process to improve wastewater nutrient removal and enhance algal lipid accumulation. Bioresour. Technol.110,448–455 (2012).
   PubMed Web of Science ®Google Scholar
• An J-Y, Sim S-J, Lee JS, Kim BW. Hydrocarbon production from secondarily treated piggery wastewater by the green alga Botryococcus braunii. J. Appl. Phycol.15,185–191 (2003).
   Web of Science ®Google Scholar
• Ji M-K, Kim H-C, Sapireddy VR et al. Simultaneous nutrient removal and lipid production from pretreated piggery wastewater by Chlorella vulgaris YSW-04. Appl. Microbiol. Biothechnol. doi:10.1007/s00253–012–4097-x (2012) (Epub ahead of print).
   Google Scholar
• Wang L, Li Y, Chen P et al. Anaerobic digested dairy manure as a nutrient supplement for cultivation of oil-rich green microalgae Chlorella sp. Bioresour. Technol.101,2623–2628 (2010).
   PubMed Web of Science ®Google Scholar
• Wang H, Xiong H, Hui Z, Zeng X. Mixotrophic cultivation of Chlorella pyrenoidosa with diluted primary piggery wastewater to produce lipids. Bioresour. Technol.104,215–220 (2012).
   PubMed Web of Science ®Google Scholar
• Kushwaha JP. Srivastava VC. Mall ID. An overview of various technologies for the treatment of dairy wastewaters. Crit. Rev. Food Sci. Nutr.51,442–452 (2011).
   PubMed Web of Science ®Google Scholar
• Chinnasamy S, Bhatnagar A, Hunt RW, Das KC. Microalgae cultivation in a wastewater dominated by carpet mill effluents for biofuel applications. Bioresour. Technol.101,3097–3105 (2010).
   PubMed Web of Science ®Google Scholar
• Hongyang S, Yalei Z, Chunmin Z, Xuefei Z, Jinpeng L. Cultivation of Chlorella pyrenoidosa in soybean processing wastewater. Bioresour. Technol.102,9884–9890 (2011).
   PubMed Web of Science ®Google Scholar
• Yamasaki T, Aki T, Shinozaki M, Taguchi M, Kawamoto S, Ono K. Utilization of Shochu distillery wastewater for production of polyunsaturated fatty acids and xanthophylls using thraustochytrid. J. Biosci. Bioeng.102,323–327 (2006).
   PubMed Web of Science ®Google Scholar
• Brennan L, Owende P. Biofuels from microalgae – a review of technologies for production, processing, and extractions of biofuels and co-products. Renew. Sust. Energy Rev.14,557–577 (2010).
   Web of Science ®Google Scholar
• Spolaore P, Joannis-Cassan C, Duran E, Isambert A. Commercial applications of microalgae. J. Biosci. Bioeng.101(2),87–96 (2006).
   PubMed Web of Science ®Google Scholar
• Schenk PM, Thomas-Hall SR, Stephens E et al. Second generation biofuels: high-efficiency microalgae for biodiesel production. Bioenergy Res1,20–43 (2008).
   Web of Science ®Google Scholar
• Posten C. Design principles of photo-bioreactors for cultivation of microalgae. Eng. Life Sci.9,165–177 (2009).
   Web of Science ®Google Scholar
• Shimamura R, Watanabe S, Sakakura Y, Shiho M, Kaya K, Watanabe MM. Development of Botryococcus seed culture system for future mass culture. Procedia Environ. Sci.15,80–89 (2012).
   Google Scholar
• Murthy GS. Overview and assessment of algal biofuels production technologies. In: Biofuels – Alternative Feedstocks and Conversion Processes. Academic Press, Waltham, MA, USA, 415–437 (2011).
   Google Scholar
• Larden L, Hèlias A, Sialve B, Steyer JP, Bernard O. Life-cycle assessment of biodiesel production from microalgae. Environ. Sci. Technol.43,6475–6481 (2009).
   PubMed Web of Science ®Google Scholar
• Stephenson AL, Kazamia E, Dennis JS, Howe CJ, Scott SA, Smith AG. Life-cycle assessment of potential algal biodiesel production in the United Kingdom: a comparison of raceways and air-lift tubular bioreactors. Energy Fuels24,4062–4077 (2010).
   Web of Science ®Google Scholar
• Campbell PK, Beer T, Batten D. Life cycle assessment of biodiesel production from microalgae in ponds. Bioresour. Technol.102,50–56 (2011).
   PubMed Web of Science ®Google Scholar
• Sander K, Murthy GS. Life cycle analysis of algae biodiesel. Int. J. Life Cycle Assess.15,704–714 (2010).
   Web of Science ®Google Scholar
• Frank ED, Han J, Palou-Rivera I, Elgowainy A, Wang MQ. Life-Cycle Analysis of Algal Lipid Fuels with the GREET Model. ANL/ESD/11–15. Energy System Division, Argonne National Laboratory, US Department of Energy, Lemont, IL, USA (2011).
   Google Scholar
• Liu X, Clarens AF, Colosi LM. Algae biodiesel has potential despite inconclusive results to date. Bioresour. Technol.104,803–806 (2012).
   PubMed Web of Science ®Google Scholar
• Grierson S, Strezov V. Life cycle assessment of the microalgae biofuel value chain. Presented at: Binature 2012: The Third International Conference of Bioenvironment, Biodiversity and Renewable Energies. St Maarten, The Netherlands, 25–30 March 2012.
   Google Scholar
• Benemann JR, Oswald WJ. Systems and Economic Analysis of Microalgae Ponds for Conversion of CO2 to Biomass. Final Report to the Department of Energy. Pittsburg Energy Technology Center, Pittsburg, PA, USA (1996).
   Google Scholar
• Lundquist TJ, Woertz, IC, Quinn NWT, Benemann JR. A Realistic Technology and Engineering Assessment of Algae Biofuel Production. Energy Biosciences Institute, University of California, Berkeley, CA, USA (2010).
   Google Scholar
• Norsker NH, Barbosa MJ, Vermue MH, Wijffels R. Microalgal production – close look at the economics. Biotechnol. Adv.29,24–27 (2011).
   PubMed Web of Science ®Google Scholar
• Norton TA, Michael Melkonian M, Andersen RA. Algal biodiversity. Phycologia35(4),308–326 (1996).
   Web of Science ®Google Scholar
• Shiho M, Kawachi M, Horioka K et al. Business evaluation of an oil production system with green micro-algae Botryococcus braunii. Procedia Environ. Sci.15,90–109 (2012).
   Google Scholar
• Brealey RA, Myers ST, Allen F. Principles of Corporate Finance. McGraw-Hill International, NY, USA (2008).
   Google Scholar
• Hiller D, Ross S, Westerfield R, Jaffe J, Jordan B. Corporate Finance. McGraw-Hill Education, Maidenhead, UK (2010).
   Google Scholar
• International Energy Agency. World Energy Outlook 2006. International Energy Agency/OECD, Paris, France (2006).
   Google Scholar
• International Energy Agency. World Energy Outlook 2007. International Energy Agency/OECD, Paris, France (2007).
   Google Scholar
• International Energy Agency. World Energy Outlook 2008. International Energy Agency/OECD, Paris, France (2008).
   Google Scholar
• International Energy Agency. World Energy Outlook 2009. International Energy Agency/OECD, Paris, France (2009).
   Google Scholar
• International Energy Agency. World Energy Outlook 2010. International Energy Agency/OECD, Paris, France (2010).
   Google Scholar
• Weyer K, Bush DR, Darzins A, Wilson BD. Theoretical maximum algal oil production. Bioenergy Res.3,204–213 (2010).
   Web of Science ®Google Scholar
• Eroglu E, Okada S, Melis A. Hydrocarbon productivities in different Botryococcus strains: comparative methods in product quantification. J. Appl. Phycol.23,763–775 (2011).
   PubMed Web of Science ®Google Scholar
• Rodolfi L, Chini Zittelli G, Bassi N et al. Microalgae for oil: strain selection, induction of lipid synthesis and outdoor mass cultivation in a low-cost photobioreactor. Biotechnol. Bioeng.102,100–112 (2009).
   PubMed Web of Science ®Google Scholar
• Gouveia L, Oliveira AC. Microalgae as a raw material for biofuels production. J. Ind. Microbiol. Biotechnol.36,269–274. (2009).
   PubMed Web of Science ®Google Scholar
• Chen Y, Wang J, Liu T, Gao L. Effects of initial population density (IPD) on growth and lipid composition of Nannochloropsis sp. J. Appl. Phycol. (2012) (Epub ahead of print).
   Google Scholar
• Li Y, Horsman M, Wang B, Wu N, Lan CQ. Effects of nitrogen sources on cell growth and lipid accumulation of green alga Neochloris oleoabundans. Appl. Microbiol. Biotechnol.81,629–636 (2008).
   PubMed Web of Science ®Google Scholar
• Satoh A, Kato M, Yamato K et al. Characterization of the lipid accumulation in a new microalgal species, Pseudochoricystis ellipsoidea (Trebouxiophyceae). J. Jpn Inst. Energy89,909–913 (2010).
   Google Scholar
• Tucci S, Vacula R, Krajcovic J, Proksch P, Martin W. Variability of wax ester fermentation in natural and bleached Euglena gracilis strains in response to oxygen and the elongase inhibitor flufenacet. J. Eukaryot. Microbiol.57,63–69 (2010).
   PubMed Web of Science ®Google Scholar

▪ Patent

• Kurano N, Sekiguchi H, Sato A, Matsuda S, Adachi K, Atsumi M: US7981648 B2 (2011).
   Google Scholar

▪ Websites

• Solazyme. http://solazyme.com
   Google Scholar
• Algenol Biofuels. www.algenolbiofuels.com
   Google Scholar
• Biofuels Digest. Solazyme files $100M IPO. www.biofuelsdigest.com/bdigest/2011/03/15/solazyme-files-100m-ipo
   Google Scholar