Chlamydomonas as a model for biofuels and bio‐products production
Open accessAbstract
Summary: Developing renewable energy sources is critical to maintaining the economic growth of the planet while protecting the environment. First generation biofuels focused on food crops like corn and sugarcane for ethanol production, and soybean and palm for biodiesel production. Second generation biofuels based on cellulosic ethanol produced from terrestrial plants, has received extensive funding and recently pilot facilities have been commissioned, but to date output of fuels from these sources has fallen well short of what is needed. Recent research and pilot demonstrations have highlighted the potential of algae as one of the most promising sources of sustainable liquid transportation fuels. Algae have also been established as unique biofactories for industrial, therapeutic, and nutraceutical co‐products. Chlamydomonas reinhardtii 's long established role in the field of basic research in green algae has paved the way for understanding algal metabolism and developing genetic engineering protocols. These tools are now being utilized in C. reinhardtii and in other algal species for the development of strains to maximize biofuels and bio‐products yields from the lab to the field.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Open systems encompass a range of setups, including small artificial ponds and large bodies of open water, each employing various agitation systems.
“Open systems encompass a range of setups, including small artificial ponds and large bodies of open water, each employing various agitation systems [160].”
From Microalgae biofuels: illuminating the path to a sustainable future amidst challenges and opportunities (2024) · cites this paper as [160]
The OUTDOOR CULTIVATION SYSTEMS section says open systems range from small artificial ponds to large open bodies of water. It does not say that these setups employ various agitation systems; a further search for “agitation” found no supporting passage. Page information was not available in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredPhotobioreactors allow for a wider selection of microalgae species, while open systems typically lead to the cultivation of only a few robust photoautotrophic species.
“PBRs allow for a wider selection of microalgae species, while open systems typically lead to the cultivation of only a few robust photoautotrophic species [160].”
From Microalgae biofuels: illuminating the path to a sustainable future amidst challenges and opportunities (2024) · cites this paper as [160]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Faulkner, D. J. (1990) · Natural Product Reports · doi:10.1039/np9900700269 · Cited by 4,880 · see citing works
Lipid productivity as a key characteristic for choosing algal species for biodiesel production
Griffiths, M. J., & Harrison, S. T. L. (2009) · Journal of Applied Phycology · doi:10.1007/s10811-008-9392-7 · Cited by 1,421 · see citing works
Jiang, W., Zhou, H., Bi, H., Fromm, M., Yang, B., & Weeks, D. P. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt780 · Cited by 1,250 · see citing works
Photobioreactors for Mass Cultivation of Algae
Ugwu, C. U., Aoyagi, H., & Uchiyama, H. (2008) · Bioresource Technology · doi:10.1016/j.biortech.2007.01.046 · Cited by 1,209 · see citing works
Melis, A., Zhang, L., Forestier, M., Ghirardi, M. L., & Seibert, M. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.122.1.127 · Cited by 1,110 · see citing works
Importance of algae oil as a source of biodiesel
Demirbaş, A., & Demirbas, M. F. (2010) · Energy Conversion and Management · doi:10.1016/j.enconman.2010.06.055 · Cited by 1,031 · see citing works
Biopharmaceutical benchmarks 2014
Walsh, G. (2014) · Nature Biotechnology · doi:10.1038/nbt.3040 · Cited by 1,008 · see citing works
Chloroplast Transformation in Chlamydomonas with High Velocity Microprojectiles
Boynton, J. E., Gillham, N. W., Harris, E. H., Hosler, J. P., Johnson, A. M., Jones, A. R., Randolph-Anderson, B. L., Robertson, D., Klein, T. M., Shark, K. B., et al. (1988) · Science · doi:10.1126/science.2897716 · Cited by 963 · see citing works
Siaut, M., Cuiné, S., Cagnon, C., Fessler, B., Nguyen, H. M., Carrier, P., Beyly, A., Beisson, F., Triantaphylidès, C., Li‐Beisson, Y., et al. (2011) · BMC Biotechnology · doi:10.1186/1472-6750-11-7 · Cited by 754 · see citing works
Outdoor cultivation of microalgae for carotenoid production: Current state and perspectives
Del Campo, J. A., García-González, M., & Guerrero, M. G. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-0844-9 · Cited by 739 · see citing works
Aquatic phototrophs: efficient alternatives to land-based crops for biofuels
Dismukes, G. C., Carrieri, D., Bennette, N., Ananyev, G. M., & Posewitz, M. C. (2008) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2008.05.007 · Cited by 733 · see citing works
Exploiting diversity and synthetic biology for the production of algal biofuels
Georgianna, D. R., & Mayfield, S. P. (2012) · Nature · doi:10.1038/nature11479 · Cited by 713 · see citing works
Self-citationIdentification and microbial production of a terpene-based advanced biofuel
Peralta‐Yahya, P., Ouellet, M., Chan, R., Mukhopadhyay, A., Keasling, J. D., & Lee, T. S. (2011) · Nature Communications · doi:10.1038/ncomms1494 · Cited by 638 · see citing works
Wang, Z. T., Ullrich, N., Joo, S., Waffenschmidt, S., & Goodenough, U. W. (2009) · Eukaryotic Cell · doi:10.1128/ec.00272-09 · Cited by 542 · see citing works
Molecular mechanisms of DNA double-strand break repair
Kanaar, R., Hoeijmakers, J. H. J., & van Gent, D. C. (1998) · Trends in Cell Biology · doi:10.1016/s0962-8924(98)01383-x · Cited by 526 · see citing works
Blunt, J. W., Copp, B. R., Keyzers, R. A., Munro, M. H. G., & Prinsep, M. R. (2011) · Natural Product Reports · doi:10.1039/c2np00090c · Cited by 482 · see citing works
Mechanism and challenges in commercialisation of algal biofuels
Singh, A., Nigam, P. S., & Murphy, J. D. (2011) · Bioresource Technology · doi:10.1016/j.biortech.2010.06.057 · Cited by 476 · cited 5× · see citing works
“Raceways can be constructed relatively cheaply and require little maintenance (Singh et al., 2011; Schoepp et al., 2014).”
BackgroundInfluentialBoyle, N. R., Page, M. D., Liu, B., Blaby, I. K., Casero, D., Kropat, J., Cokus, S. J., Hong‐Hermesdorf, A., Shaw, J., Karpowicz, S. J., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.334052 · Cited by 416 · see citing works
Li, T., Huang, S., Zhao, X., Wright, D. A., Carpenter, S. L., Spalding, M. H., Weeks, D. P., & Yang, B. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr188 · Cited by 414 · see citing works
Moellering, E. R., & Christoph Benning, A. (2009) · Eukaryotic Cell · doi:10.1128/ec.00203-09 · Cited by 401 · see citing works
Algae biofuels: versatility for the future of bioenergy
Jones, C. S., & Mayfield, S. P. (2011) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2011.10.013 · Cited by 400 · see citing works
Self-citationMsanne, J., Xu, D., Konda, A. R., Casas-Mollano, J. A., Awada, T. N., Cahoon, E. B., & Cerutti, H. D. (2012) · Phytochemistry · doi:10.1016/j.phytochem.2011.12.007 · Cited by 389 · see citing works
Li, Y., Han, D., Hu, G., Dauvillée, D., Sommerfeld, M. R., Ball, S. G., & Hu, Q. (2010) · Metabolic Engineering · doi:10.1016/j.ymben.2010.02.002 · Cited by 384 · see citing works
Hydrogenases and Hydrogen Photoproduction in Oxygenic Photosynthetic Organisms
Ghirardi, M. L., Posewitz, M. C., Maness, P., Dubini, A., Yu, J., & Seibert, M. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.58.032806.103848 · Cited by 371 · see citing works
Successful Transient Expression of Cas9 and Single Guide RNA Genes in Chlamydomonas reinhardtii
Jiang, W., Brueggeman, A. J., Horken, K. M., Plucinak, T. M., & Weeks, D. P. (2014) · Eukaryotic Cell · doi:10.1128/ec.00213-14 · Cited by 361 · see citing works
Work, V. H., Radakovits, R., Jinkerson, R. E., Meuser, J. E., Elliott, L. G., Vinyard, D. J., Laurens, L. M. L., Dismukes, G. C., & Posewitz, M. C. (2010) · Eukaryotic Cell · doi:10.1128/ec.00075-10 · Cited by 351 · see citing works
The HSP70A promoter as a tool for the improved expression of transgenes in Chlamydomonas
Schroda, M., Blöcker, D., & Beck, C. F. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00652.x · Cited by 349 · see citing works
Molnár, A., Bassett, A. R., Thuenemann, E. C., Schwach, F., Karkare, S., Ossowski, S., Weigel, D., & Baulcombe, D. C. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03767.x · Cited by 345 · see citing works
Unraveling the genomic mosaic of a ubiquitous genus of marine cyanobacteria
Dufresne, A., Ostrowski, M. D., Scanlan, D. J., Garczarek, L., Mazard, S., Palenik, B. P., Paulsen, I. T., de Marsac, N. T., Wincker, P., Dossat, C., et al. (2008) · Genome biology · doi:10.1186/gb-2008-9-5-r90 · Cited by 338 · see citing works
Merchant, S., Kropat, J., Liu, B., Shaw, J., & Warakanont, J. (2011) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2011.12.001 · Cited by 337 · see citing works
Rasala, B. A., & Mayfield, S. P. (2014) · Photosynthesis Research · doi:10.1007/s11120-014-9994-7 · Cited by 289 · see citing works
Self-citationNäätsaari, L., Mistlberger, B., Rüth, C., Hajek, T., Hartner, F. S., & Glieder, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039720 · Cited by 281 · see citing works
Transgene and Transposon Silencing in Chlamydomonas reinhardtii by a DEAH-Box RNA Helicase
Wu‐Scharf, D., Jeong, B., Zhang, C. H., & Cerutti, H. D. (2000) · Science · doi:10.1126/science.290.5494.1159 · Cited by 280 · see citing works
Algal biofuels: Challenges and opportunities
Leite, G. B., Abdelaziz, A. E. M., & Hallenbeck, P. C. (2013) · Bioresource Technology · doi:10.1016/j.biortech.2013.02.007 · Cited by 274 · see citing works
Rasala, B. A., Muto, M., Lee, P. A., Jager, M., Cardoso, R. M. F., Behnke, C. A., Kirk, P. B., Hokanson, C. A., Crea, R., Mendez, M. J., et al. (2010) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2010.00503.x · Cited by 271 · see citing works
Self-citationNorton, T. A., Melkonian, M., & Andersen, R. A. (1996) · Phycologia · doi:10.2216/i0031-8884-35-4-308.1 · Cited by 271 · see citing works
Goodson, C. M., Roth, R. A., Wang, Z. T., & Goodenough, U. W. (2011) · Eukaryotic Cell · doi:10.1128/ec.05242-11 · Cited by 252 · see citing works
Mulo, P., Sakurai, I., & Aro, E. (2011) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2011.04.011 · Cited by 251 · see citing works
Rasala, B. A., Lee, P. A., Shen, Z., Briggs, S. P., Mendez, M. J., & Mayfield, S. P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043349 · Cited by 234 · see citing works
Self-citationZhang, R., Patena, W., Armbruster, U., Gang, S. S., Blum, S. R., & Jonikas, M. C. (2014) · The Plant Cell · doi:10.1105/tpc.114.124099 · Cited by 223 · see citing works
Edible oils from microalgae: insights in TAG accumulation
Klok, A. J., Lamers, P. P., Martens, D. E., Draaisma, R. B., & Wijffels, R. H. (2014) · Trends in biotechnology · doi:10.1016/j.tibtech.2014.07.004 · Cited by 219 · see citing works
Fatty acid profiling of Chlamydomonas reinhardtii under nitrogen deprivation
James, G. O., Hocart, C. H., Hillier, W., Chen, H., Kordbacheh, F., Price, G. D., & Djordjevic, M. A. (2010) · Bioresource Technology · doi:10.1016/j.biortech.2010.11.051 · Cited by 213 · see citing works
An updated comprehensive techno-economic analysis of algae biodiesel
Nagarajan, S., Chou, S. K., Cao, S., Wu, C., & Zhou, Z. (2012) · Bioresource Technology · doi:10.1016/j.biortech.2012.11.108 · Cited by 211 · see citing works
Epigenetic silencing of a foreign gene in nuclear transformants of Chlamydomonas.
Cerutti, H. D., Johnson, A. M., Gillham, N. W., & Boynton, J. E. (1997) · The Plant Cell · doi:10.1105/tpc.9.6.925 · Cited by 206 · see citing works
Microalgae for a macroenergy world
Öncel, S. Ş. (2013) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2013.05.059 · Cited by 204 · see citing works
Cordero, B. F., Couso, I., León, R., Rodrı́guez, H., & Vargas, M. A. (2011) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-011-3262-y · Cited by 190 · see citing works
Production of unique immunotoxin cancer therapeutics in algal chloroplasts
Tran, M., Van, C., Barrera, D. J., Pettersson, P. L., Peinado, C. D., Bui, J. D., & Mayfield, S. P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214638110 · Cited by 186 · see citing works
Self-citationRussa, M. L., Bogen, C., Uhmeyer, A., Doebbe, A., Filippone, E., Kruse, O., & Mussgnug, J. H. (2012) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2012.04.006 · Cited by 184 · see citing works
Genomic Insights into Marine Microalgae
Parker, M. S., Mock, T., & Armbrust, E. V. (2008) · Annual Review of Genetics · doi:10.1146/annurev.genet.42.110807.091417 · Cited by 182 · see citing works
Strategies to facilitate transgene expression in Chlamydomonas reinhardtii
Eichler-Stahlberg, A., Weisheit, W., Ruecker, O., & Heitzer, M. (2009) · Planta · doi:10.1007/s00425-008-0879-x · Cited by 178 · see citing works
Heat-stable oral alga-based vaccine protects mice from Staphylococcus aureus infection
Dreesen, I. A. J., Hamri, G. C., & Fussenegger, M. (2009) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2009.12.006 · Cited by 177 · see citing works
Synthetic promoters: genetic control through cis engineering
Venter, M. (2007) · Trends in Plant Science · doi:10.1016/j.tplants.2007.01.002 · Cited by 170 · see citing works
Plants as bioreactors for protein production: avoiding the problem of transgene silencing
Wilde, C. D., Houdt, H. V., Buck, S. D., Angenon, G., Jaeger, G. D., & Depicker, A. (2000) · Plant Molecular Biology · doi:10.1023/a:1006464304199 · Cited by 164 · see citing works
Gene silencing by artificial microRNAs in Chlamydomonas
Zhao, T., Wang, W., Bai, X., & Qi, Y. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03758.x · Cited by 162 · see citing works
The Path to Triacylglyceride Obesity in the sta6 Strain of Chlamydomonas reinhardtii
Goodenough, U. W., Blaby, I. K., Casero, D., Gallaher, S. D., Goodson, C. M., Johnson, S. L., Lee, J.-H., Merchant, S., Pellegrini, M. A., Roth, R. A., et al. (2014) · Eukaryotic Cell · doi:10.1128/ec.00013-14 · Cited by 160 · see citing works
Torzillo, G., Scoma, A., Faraloni, C., Ena, A., & Johanningmeier, U. (2008) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2008.07.093 · Cited by 155 · see citing works
Robust expression of a bioactive mammalian protein in <i>Chlamydomonas</i> chloroplast
Manuell, A. L., Beligni, M. V., Elder, J. H., Siefker, D. T., Tran, M., Weber, A., McDonald, T. L., & Mayfield, S. P. (2007) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2007.00249.x · Cited by 154 · see citing works
Self-citationHomologous recombination in the nuclear genome of Chlamydomonas reinhardtii.
Sodeinde, O. A., & Kindle, K. L. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.19.9199 · Cited by 141 · see citing works
Minai, L., Wostrikoff, K., Wollman, F.-A., & Choquet, Y. (2005) · The Plant Cell · doi:10.1105/tpc.105.037705 · Cited by 141 · see citing works
Rasala, B. A., Barrera, D. J., Ng, J. Y., Plucinak, T. M., Rosenberg, J. N., Weeks, D. P., Oyler, G. A., Peterson, T. C., Haerizadeh, F., & Mayfield, S. P. (2013) · The Plant Journal · doi:10.1111/tpj.12165 · Cited by 137 · see citing works
Self-citationDecoding algal genomes: tracing back the history of photosynthetic life on Earth.
Tirichine, L., & Bowler, C. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04540.x · Cited by 134 · see citing works
Kim, D.-H., Kim, Y. T., Cho, J. J., Bae, J.-H., Hur, S. B., Hwang, I., & Choi, T. (2002) · Marine Biotechnology · doi:10.1007/s1012601-0070-x · Cited by 134 · see citing works
Rosales‐Mendoza, S., Paz-Maldonado, L. M. T., & Soria‐Guerra, R. E. (2011) · Plant Cell Reports · doi:10.1007/s00299-011-1186-8 · Cited by 133 · see citing works
Alga-Produced Cholera Toxin-Pfs25 Fusion Proteins as Oral Vaccines
Gregory, J. A., Topol, A. B., Doerner, D. Z., & Mayfield, S. P. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.00714-13 · Cited by 132 · see citing works
Self-citationManipulating Fatty Acid Biosynthesis in Microalgae for Biofuel through Protein-Protein Interactions
Blatti, J. L., Beld, J., Behnke, C. A., Mendez, M. J., Mayfield, S. P., & Burkart, M. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042949 · Cited by 127 · see citing works
Self-citationRasala, B. A., & Mayfield, S. P. (2011) · Bioengineered Bugs · doi:10.4161/bbug.2.1.13423 · Cited by 122 · see citing works
Self-citationCouso, I., Vilà, M., Rodrı́guez, H., Vargas, M. A., & León, R. (2010) · Biotechnology Progress · doi:10.1002/btpr.527 · Cited by 118 · see citing works
Deng, X., Gu, B., Li, Y., Hu, X., Guo, J., & Fei, X.-W. (2012) · Molecular Plant · doi:10.1093/mp/sss040 · Cited by 104 · see citing works
Kirst, H., García‐Cerdán, J. G., Zurbriggen, A., & Melis, A. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.189910 · Cited by 102 · see citing works
The future viability of algae-derived biodiesel under economic and technical uncertainties
Brownbridge, G., Azadi, P., Smallbone, A. J., Bhave, A. N., Taylor, B., & Kraft, M. (2013) · Bioresource Technology · doi:10.1016/j.biortech.2013.10.062 · Cited by 102 · see citing works
Scoma, A., Giannelli, L., Faraloni, C., & Torzillo, G. (2011) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2011.06.040 · Cited by 99 · see citing works
Terashima, M., Freeman, E. S., Jinkerson, R. E., & Jonikas, M. C. (2014) · The Plant Journal · doi:10.1111/tpj.12682 · Cited by 97 · see citing works
Efficient H2 production via Chlamydomonas reinhardtii
Esquível, M. G., Amaro, H. M., Pinto, T. S., Fevereiro, P. S., & Malcata, F. X. (2011) · Trends in biotechnology · doi:10.1016/j.tibtech.2011.06.008 · Cited by 94 · see citing works
Production of recombinant enzymes in the marine alga Dunaliella tertiolecta
Georgianna, D. R., Hannon, M. J., Marcuschi, M., Wu, S., Botsch, K., Lewis, A. J., Hyun, J. S., Mendez, M. J., & Mayfield, S. P. (2012) · Algal Research · doi:10.1016/j.algal.2012.10.004 · Cited by 88 · see citing works
Self-citationProduction of recombinant proteins in microalgae at pilot greenhouse scale
Gimpel, J. A., Hyun, J. S., Schoepp, N. G., & Mayfield, S. P. (2014) · Biotechnology and Bioengineering · doi:10.1002/bit.25357 · Cited by 86 · see citing works
Self-citationStudies on homologous recombination in the green alga Chlamydomonas reinhardtii
Gumpel, N. J., Rochaix, J., & Purton, S. (1994) · Current Genetics · doi:10.1007/bf00309931 · Cited by 84 · see citing works
Production of therapeutic proteins in the chloroplast of Chlamydomonas reinhardtii
Almaraz-Delgado, A. L., Flores‐Uribe, J., Pérez-España, V. H., Salgado, E., & Badillo-Corona, J. A. (2014) · AMB Express · doi:10.1186/s13568-014-0057-4 · Cited by 82 · see citing works
Production of anti‐cancer immunotoxins in algae: Ribosome inactivating proteins as fusion partners
Tran, M., Henry, R. E., Siefker, D. T., Van, C., Newkirk, G. M., Kim, J. J., Bui, J. D., & Mayfield, S. P. (2013) · Biotechnology and Bioengineering · doi:10.1002/bit.24966 · Cited by 79 · see citing works
Self-citationSchmollinger, S., Strenkert, D., & Schroda, M. (2010) · Current Genetics · doi:10.1007/s00294-010-0304-4 · Cited by 74 · see citing works
Targeted Disruption of the NIT8 Gene in Chlamydomonas reinhardtii
Nelson, J. A. E., & Lefebvre, P. A. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.10.5762 · Cited by 73 · see citing works
Human serum amyloid A3 peptide enhances intestinal MUC3 expression and inhibits EPEC adherence
Larson, M. A., Wei, S. H., Weber, A. M., Mack, D. R., & McDonald, T. L. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02901-7 · Cited by 73 · see citing works
System and method for research-scale outdoor production of microalgae and cyanobacteria
Schoepp, N. G., Stewart, R. L., Sun, V., Quigley, A. J., Mendola, D., Mayfield, S. P., & Burkart, M. D. (2014) · Bioresource Technology · doi:10.1016/j.biortech.2014.05.046 · Cited by 68 · see citing works
Self-citationYoon, S.-M., Kim, S. Y., Li, K. F., Yoon, B. H., Choe, S., & Kuo, M. M.-C. (2011) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-011-3279-2 · Cited by 68 · see citing works
TALE activation of endogenous genes in Chlamydomonas reinhardtii
Gao, H., Wright, D. A., Li, T., Wang, Y., Horken, K. M., Weeks, D. P., Yang, B., & Spalding, M. H. (2014) · Algal Research · doi:10.1016/j.algal.2014.05.003 · Cited by 61 · see citing works
Hydrogen Fuel Production by Transgenic Microalgae
Melis, A., Seibert, M., & Ghirardi, M. L. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-75532-8_10 · Cited by 53 · see citing works
Expression of human soluble TRAIL in Chlamydomonas reinhardtii chloroplast
Yang, Z., Li, Y., Chen, F., Li, D., Zhang, Z., Liu, Y., Zheng, D., Wang, Y., & Shen, G. (2006) · Chinese Science Bulletin · doi:10.1007/s11434-006-2041-0 · Cited by 53 · see citing works
Öncel, S. Ş., Köse, A., Faraloni, C., İmamoğlu, E., Elibol, M., Torzillo, G., & Sukan, F. V. (2014) · Biochemical Engineering Journal · doi:10.1016/j.bej.2014.06.019 · Cited by 53 · see citing works
Baltz, A., Dang, K.-V., Beyly, A., Auroy, P., Richaud, P., Cournac, L., & Peltier, G. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.240432 · Cited by 53 · see citing works
High‐value Recombinant Protein Production in Microalgae
Barrera, D. J., & Mayfield, S. P. (2013) · doi:10.1002/9781118567166.ch27 · Cited by 48 · see citing works
Self-citationXie, B., Stessman, D. J., Hart, J. H., Dong, H., Wang, Y., Wright, D. A., Nikolau, B. J., Spalding, M. H., & Halverson, L. J. (2014) · Plant Biotechnology Journal · doi:10.1111/pbi.12190 · Cited by 45 · see citing works
Mack, D. R., McDonald, T. L., Larson, M. A., Wei, S. H., & Weber, A. M. (2003) · Pediatric Research · doi:10.1203/00006450-200301000-00023 · Cited by 45 · see citing works
Natural Variants of Photosystem II Subunit D1 Tune Photochemical Fitness to Solar Intensity *
Vinyard, D. J., Gimpel, J. A., Ananyev, G., Cornejo, M. A., Golden, S. S., Mayfield, S. P., & Dismukes, G. C. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.394668 · Cited by 40 · see citing works
Self-citationSpecht, E. A., & Mayfield, S. P. (2012) · ACS Synthetic Biology · doi:10.1021/sb300069k · Cited by 40 · see citing works
Self-citationVinyard, D. J., Gimpel, J. A., Ananyev, G., Mayfield, S. P., & Dismukes, G. C. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5002967 · Cited by 38 · see citing works
Self-citationSu, Z., Qian, K., Tan, C.-P., Meng, C., & Qin, S. (2005) · Acta Biochimica et Biophysica Sinica · doi:10.1111/j.1745-7270.2005.00092.x · Cited by 36 · see citing works
Technoeconomic Boundary Analysis of Biological Pathways to Hydrogen Production
James, B. D., Fuel Cell Technologies Office (EE-3F) USDOE Office of Energy Efficiency and Renewable Energy (EERE), Baum, G. N., Perez, J., & Baum, K. N. (2009) · doi:10.2172/1218404 · Cited by 35 · see citing works
Zhang, Y., Shen, G., & Ru, B. (2006) · Acta Biochimica et Biophysica Sinica · doi:10.1111/j.1745-7270.2006.00148.x · Cited by 34 · see citing works
Kato, K., Marui, T., Kasai, S., & Shinmyo, A. (2007) · Journal of Bioscience and Bioengineering · doi:10.1263/jbb.104.207 · Cited by 31 · see citing works
Selenoprotein-Transgenic Chlamydomonas reinhardtii
Hou, Q., Qiu, S., Liu, Q., Tian, J., Hu, Z., & Ni, J. (2013) · Nutrients · doi:10.3390/nu5030624 · Cited by 29 · see citing works
Genetic Engineering to Improve Algal Biofuels Production
Rasala, B. A., Gimpel, J. A., Tran, M., Hannon, M. J., Miyake-Stoner, S. J., Specht, E. A., & Mayfield, S. P. (2012) · Springer eBooks · doi:10.1007/978-94-007-5479-9_6 · Cited by 24 · see citing works
Self-citationHydrogen Production byChlamydomonas reinhardtii
Torzillo, G., & Seibert, M. (2013) · Wiley eBooks · doi:10.1002/9781118567166.ch22 · Cited by 20 · see citing works
Jiang, W., Cossey, S. M., Rosenberg, J. N., Oyler, G. A., Olson, B. J. S. C., & Weeks, D. P. (2014) · BMC Plant Biology · doi:10.1186/s12870-014-0244-0 · Cited by 16 · see citing works
Xu, L., Wang, Q., Wu, S., & Li, D. (2014) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2014.04.178 · Cited by 10 · see citing works
Flagged first, then by citations
1 of the 104 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Torzillo G Seibert M 2013 Hydrogen production by Chlamydomonas reinhardtii Handbook of Microalgal Culture: Applied Phycology and Biotechnology 2nd Richmond A Hu Q Oxford, UK John Wiley & Sons, Ltd 417 432
Cited by
Sorted by citations
Current status and applications of genome-scale metabolic models
Gu, C., Kim, G. B., Kim, W. J., Kim, H. U., & Lee, S. Y. (2019) · Genome biology · doi:10.1186/s13059-019-1730-3 · Cited by 765 · see citing works
Carotenoids from microalgae: A review of recent developments
Gong, M., & Bassi, A. S. (2016) · Biotechnology Advances · doi:10.1016/j.biotechadv.2016.10.005 · Cited by 727 · see citing works
Biomass from microalgae: the potential of domestication towards sustainable biofactories
Benedetti, M., Vecchi, V., Barera, S., & Dall’Osto, L. (2018) · Microbial Cell Factories · doi:10.1186/s12934-018-1019-3 · Cited by 366 · see citing works
Fatty Acid and Lipid Transport in Plant Cells
Li, N., Xu, C., Li‐Beisson, Y., & Philippar, K. (2015) · Trends in Plant Science · doi:10.1016/j.tplants.2015.10.011 · Cited by 298 · see citing works
Crozet, P., Navarro, F. J., Willmund, F., Mehrshahi, P., Bakowski, K., Lauersen, K. J., Pérez-Pérez, M.-E., Auroy, P., Gorchs Rovira, A., Sauret-Gueto, S., et al. (2018) · ACS Synthetic Biology · doi:10.1021/acssynbio.8b00251 · Cited by 297 · see citing works
Biofuel production from microalgae: challenges and chances
Hoang, A. T., Sirohi, R., Pandey, A., Nižetić, S., Lam, S. S., Chen, W., Luque, R., Thomas, S., Arıcı, M., & Pham, V. V. (2022) · Phytochemistry Reviews · doi:10.1007/s11101-022-09819-y · Cited by 296 · see citing works
A new insight into cell walls of Chlorophyta
Baudelet, P.-H., Ricochon, G., Linder, M., & Muniglia, L. (2017) · Algal Research · doi:10.1016/j.algal.2017.04.008 · Cited by 269 · see citing works
Chugh, M., Kumar, L., Shah, M. P., & Bharadvaja, N. (2022) · Energy Nexus · doi:10.1016/j.nexus.2022.100129 · Cited by 222 · see citing works
Gimpel, J. A., Henríquez, V., & Mayfield, S. P. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01376 · Cited by 207 · see citing works
Self-citationFerenczi, Á., Pyott, D. E., Xipnitou, A., & Molnár, A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1710597114 · Cited by 205 · see citing works
Multiomics resolution of molecular events during a day in the life of Chlamydomonas
Strenkert, D., Schmollinger, S., Gallaher, S. D., Salomé, P. A., Purvine, S. O., Nicora, C., Mettler‐Altmann, T., Soubeyrand, E., Weber, A. P. M., Lipton, M. S. W., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1815238116 · Cited by 204 · see citing works
Wang, M., Ye, X., Bi, H., & Shen, Z. (2024) · Biotechnology for Biofuels and Bioproducts · doi:10.1186/s13068-024-02461-0 · Cited by 201 · see citing works
“Open systems encompass a range of setups, including small artificial ponds and large bodies of open water, each employing various agitation systems [160].”
BackgroundDeveloping algae as a sustainable food source
Diaz, C. J., Douglas, K. J., Kang, K., Kolarik, A. L., Malinovski, R., Torres-Tiji, Y., Molino, J. V., Badary, A., & Mayfield, S. P. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1029841 · Cited by 194 · see citing works
Self-citationStructural insight into light harvesting for photosystem II in green algae
Sheng, X., Watanabe, A., Li, A., Kim, E., Song, C., Murata, K., Song, D., Minagawa, J., & Liu, Z. (2019) · Nature Plants · doi:10.1038/s41477-019-0543-4 · Cited by 186 · see citing works
Gastrointestinal tract drug delivery using algae motors embedded in a degradable capsule
Zhang, F., Li, Z., Duan, Y., Abbas, A. K., Mundaca‐Uribe, R., Yin, L., Luan, H., Gao, W., Fang, R. H., Zhang, L., et al. (2022) · Science Robotics · doi:10.1126/scirobotics.abo4160 · Cited by 174 · see citing works
Molecular techniques to interrogate and edit the Chlamydomonas nuclear genome
Jinkerson, R. E., & Jonikas, M. C. (2015) · The Plant Journal · doi:10.1111/tpj.12801 · Cited by 162 · see citing works
Green microalgae biomolecule separations and recovery
Dixon, C. K., & Wilken, L. R. (2018) · Bioresources and Bioprocessing · doi:10.1186/s40643-018-0199-3 · Cited by 150 · see citing works
Baek, K., Yu, J., Jeong, J., Sim, S. J., Bae, S., & Jin, E. (2017) · Biotechnology and Bioengineering · doi:10.1002/bit.26499 · Cited by 147 · see citing works
Strategies to enhance production of microalgal biomass and lipids for biofuel feedstock
Chu, W.-L. (2017) · European Journal of Phycology · doi:10.1080/09670262.2017.1379100 · Cited by 146 · see citing works
Sustainable Biohydrogen Production by Chlorella sp. Microalgae: A Review
Jiménez-Llanos, J., Ramírez-Carmona, M., Rendón-Castrillón, L., & Ocampo-López, C. (2020) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2020.01.059 · Cited by 144 · see citing works
Biohybrid Microalgae Robots: Design, Fabrication, Materials, and Applications
Zhang, F., Li, Z., Chen, C., Luan, H., Fang, R. H., Zhang, L., & Wang, J. (2023) · Advanced Materials · doi:10.1002/adma.202303714 · Cited by 132 · see citing works
Gallaher, S. D., Fitz‐Gibbon, S. T., Strenkert, D., Purvine, S. O., Pellegrini, M. A., & Merchant, S. (2017) · The Plant Journal · doi:10.1111/tpj.13788 · Cited by 125 · see citing works
Couso, I., Evans, B. S., Li, J., Liu, Y., Ma, F., Diamond, S., Allen, D. K., & Umen, J. (2016) · The Plant Cell · doi:10.1105/tpc.16.00351 · Cited by 102 · see citing works
Solar biofuels production with microalgae
Hallenbeck, P. C., Grogger, M. L. M., Mraz, M., & Veverka, D. (2016) · Applied Energy · doi:10.1016/j.apenergy.2016.06.024 · Cited by 109 · see citing works
Effects of the microalgae Chlamydomonas on gastrointestinal health
Fields, F. J., Lejzerowicz, F., Schroeder, D., Ngoi, S. M., Tran, M., McDonald, D., Jiang, L., Chang, J. T., Knight, R., & Mayfield, S. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2019.103738 · Cited by 104 · see citing works
Self-citationKumar, S., Tirlangi, S., Kumar, A., Imran, M., Jai Shanker Pillai, H. P., Koshariya, A. K., Sathish, T., Ubaidullah, M., Ayub, R., Reddy, V. R. M., et al. (2023) · Sustainable Energy Technologies and Assessments · doi:10.1016/j.seta.2023.103498 · Cited by 104 · see citing works
Leveraging algal omics to reveal potential targets for augmenting TAG accumulation
Arora, N., Pienkos, P. T., Pruthi, V., Poluri, K. M., & Guarnieri, M. T. (2018) · Biotechnology Advances · doi:10.1016/j.biotechadv.2018.04.005 · Cited by 98 · see citing works
Chlamydomonas reinhardtii: A Factory of Nutraceutical and Food Supplements for Human Health
Masi, A., Leonelli, F., Scognamiglio, V., Gasperuzzo, G., Antonacci, A., & Terzidis, M. A. (2023) · Molecules · doi:10.3390/molecules28031185 · Cited by 96 · see citing works
Neupert, J., Gallaher, S. D., Lu, Y., Strenkert, D., Segal, N., Barahimipour, R., Fitz‐Gibbon, S. T., Schroda, M., Merchant, S., & Bock, R. (2020) · Nature Communications · doi:10.1038/s41467-020-19983-4 · Cited by 100 · see citing works
Brodie, J. A., Chan, C. X., Clerck, O. D., Cock, J. M., Coelho, S. M., Gachon, C. M. M., Grossman, A. R., Möck, T., Raven, J. A., Smith, A. G., et al. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2017.05.005 · Cited by 94 · see citing works
Current trends and prospects in microalgae-based bioenergy production
Bhushan, S., Kalra, A., Şimşek, H., Kumar, G., & Prajapati, S. K. (2020) · Journal of environmental chemical engineering · doi:10.1016/j.jece.2020.104025 · Cited by 95 · see citing works
Exploring the potential of microalgae in the recycling of dairy wastes
Gramegna, G., Scortica, A., Scafati, V., Ferella, F., Gurrieri, L., Giovannoni, M., Bassi, R., Sparla, F., Mattei, B., & Benedetti, M. (2020) · Bioresource Technology Reports · doi:10.1016/j.biteb.2020.100604 · Cited by 97 · see citing works
Good News for Nuclear Transgene Expression in Chlamydomonas
Schroda, M. (2019) · Cells · doi:10.3390/cells8121534 · Cited by 89 · see citing works
Barahimipour, R., Neupert, J., & Bock, R. (2016) · Plant Molecular Biology · doi:10.1007/s11103-015-0425-8 · Cited by 90 · see citing works
Guihéneuf, F., Khan, A. A., & Tran, L. P. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00400 · Cited by 89 · see citing works
Kim, H. S., Hsu, S., Han, S., Thapa, H. R., Guzman, A. R., Browne, D. R., Tatli, M., Devarenne, T. P., Stern, D. B., & Han, A. (2017) · Plant Direct · doi:10.1002/pld3.11 · Cited by 86 · see citing works
Tan, K. W. M., & Lee, Y. K. (2017) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2017.03.004 · Cited by 79 · see citing works
Boboescu, I. Z., Gherman, V. D., Lakatos, G., Pap, B., Bíró, T., & Maróti, G. (2016) · Bioresource Technology · doi:10.1016/j.biortech.2015.12.083 · Cited by 78 · see citing works
Macular pigment-enriched oil production from genome-edited microalgae
Song, I., Kim, S.-B., Kim, J., Oh, H., Jang, J.-H., Jeong, S. J., Baek, K., Shin, W., Sim, S. J., & Jin, E. (2022) · Microbial Cell Factories · doi:10.1186/s12934-021-01736-7 · Cited by 71 · see citing works
Fed-batch mixotrophic cultivation of Chlamydomonas reinhardtii for high-density cultures
Fields, F. J., Ostrand, J. T., & Mayfield, S. P. (2018) · Algal Research · doi:10.1016/j.algal.2018.05.006 · Cited by 66 · see citing works
Self-citationLi, M., van Zee, M., Riche, C. T., Tofig, B., Gallaher, S. D., Merchant, S., Damoiseaux, R. D., Goda, K., & Carlo, D. D. (2018) · Small · doi:10.1002/smll.201803315 · Cited by 65 · see citing works
Nitrogen-dependent coordination of cell cycle, quiescence and TAG accumulation in Chlamydomonas
Takeuchi, T., & Benning, C. (2019) · Biotechnology for Biofuels · doi:10.1186/s13068-019-1635-0 · Cited by 63 · see citing works
Jaeger, D., Winkler, A., Mussgnug, J. H., Kalinowski, J., Goesmann, A., & Kruse, O. (2017) · Biotechnology for Biofuels · doi:10.1186/s13068-017-0882-1 · Cited by 65 · see citing works
Ion and metabolite transport in the chloroplast of algae: lessons from land plants
Marchand, J., Heydarizadeh, P., Schoefs, B., & Spetea, C. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2793-0 · Cited by 62 · see citing works
Shaikh, K. M., Nesamma, A. A., Abdin, M. Z., & Jutur, P. P. (2019) · Biotechnology for Biofuels · doi:10.1186/s13068-019-1521-9 · Cited by 62 · see citing works
Molino, J. V. D., de Carvalho, J. C. M., & Mayfield, S. P. (2018) · PLoS ONE · doi:10.1371/journal.pone.0192433 · Cited by 61 · see citing works
Self-citationEngineering Fatty Acid Biosynthesis in Microalgae: Recent Progress and Perspectives
Song, Y., Wang, F., Chen, L., & Zhang, W. (2024) · Marine Drugs · doi:10.3390/md22050216 · Cited by 58 · see citing works
Two Glycerol-3-Phosphate Dehydrogenases from Chlamydomonas Have Distinct Roles in Lipid Metabolism
Driver, T., Trivedi, D. K., McIntosh, O. A., Dean, A. P., Goodacre, R., & Pittman, J. K. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.00491 · Cited by 57 · see citing works
Pudney, A., Gandini, C., Economou, C. K., Smith, R. T., Goddard, P., Napier, J. A., Spicer, A., & Sayanova, O. V. (2019) · Scientific Reports · doi:10.1038/s41598-019-47875-1 · Cited by 56 · see citing works
Identification and Metabolite Profiling of Chemical Activators of Lipid Accumulation in Green Algae
Wase, N. V., Tu, B., Allen, J. W., Black, P. N., & Dirusso, C. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.00433 · Cited by 55 · see citing works
Guzmán-Zapata, D., Sandoval-Vargas, J. M., Macedo-Osorio, K. S., Salgado, E., Castrejón-Flores, J. L., Oliver-Salvador, M. D. C., Durán‐Figueroa, N., Nogué, F., & Badillo-Corona, J. A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20051247 · Cited by 54 · see citing works
Enhanced lipid productivity of Chlamydomonas reinhardtii with combination of NaCl and CaCl2 stresses
Hang, L. T., Mori, K., Tanaka, Y., Morikawa, M., & Toyama, T. (2020) · Bioprocess and Biosystems Engineering · doi:10.1007/s00449-020-02293-w · Cited by 49 · see citing works
Bensalem, S., Pareau, D., Cinquin, B. P., Français, O., Pioufle, B. L., & Lopes, F. (2020) · Scientific Reports · doi:10.1038/s41598-020-59404-6 · Cited by 47 · see citing works
Building a multipurpose insertional mutant library for forward and reverse genetics in Chlamydomonas
Cheng, X., Gai, L., Ke, W., Zhao, L., Lv, B., Ma, X., Xu, N., Xia, X., Deng, X., Zheng, C., et al. (2017) · Plant Methods · doi:10.1186/s13007-017-0183-5 · Cited by 46 · see citing works
Algevir: An Expression System for Microalgae Based on Viral Vectors
Bañuelos-Hernández, B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01100 · Cited by 45 · see citing works
Experimental Genome-Wide Determination of RNA Polyadenylation in Chlamydomonas reinhardtii
Bell, S. A., Shen, C., Brown, A., & Hunt, A. G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146107 · Cited by 44 · see citing works
Changko, S., Rajakumar, P. D., Young, R., & Purton, S. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10258-7 · Cited by 44 · see citing works
Akella, S., Ma, X., Bačová, R., Harmer, Z. P., Koláčková, M., Wen, X., Wright, D. A., Spalding, M. H., Weeks, D. P., & Cerutti, H. D. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab418 · Cited by 42 · see citing works
Díaz‐Santos, E., Vilà, M., Vigara, J., & León, R. (2015) · Journal of Applied Phycology · doi:10.1007/s10811-015-0706-2 · Cited by 43 · see citing works
ALCOdb: Gene Coexpression Database for Microalgae
Aoki, Y., Okamura, Y., Ohta, H., Kinoshita, K., & Obayashi, T. (2016) · Plant and Cell Physiology · doi:10.1093/pcp/pcv190 · Cited by 43 · see citing works
Adaptive responses of free‐living and symbiotic microalgae to simulated future ocean conditions
Chan, W. Y., Oakeshott, J. G., Buerger, P., Edwards, O. R., & van Oppen, M. J. H. (2021) · Global Change Biology · doi:10.1111/gcb.15546 · Cited by 41 · see citing works
Fages‐Lartaud, M., Hundvin, K., & Hohmann‐Marriott, M. F. (2022) · The Plant Journal · doi:10.1111/tpj.15970 · Cited by 39 · see citing works
Young, D. Y., & Shachar‐Hill, Y. (2020) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiaa071 · Cited by 39 · see citing works
Metabolic responses to ethanol and butanol in Chlamydomonas reinhardtii
Jiang, Y., Xiao, P., Shao, Q., Qin, H., Hu, Z., Lei, A., & Wang, J. (2017) · Biotechnology for Biofuels · doi:10.1186/s13068-017-0931-9 · Cited by 38 · see citing works
Investigation of microalgae growth on electrospun nanofiber mats
Großerhode, C., Wehlage, D., Grothe, T., Grimmelsmann, N., Fuchs, S., Hartmann, J., Mazur, P., Reschke, V., Siemens, H., Rattenholl, A., et al. (2017) · AIMS bioengineering · doi:10.3934/bioeng.2017.3.376 · Cited by 37 · see citing works
Zhao, J., Ge, Y., Liu, K., Yamaoka, Y., Zhang, D., Chi, Z., Akkaya, M. S., & Kong, F. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c05290 · Cited by 36 · see citing works
Bioinformatics applied to biotechnology: A review towards bioenergy research
de Carvalho, L. M., Borelli, G., Camargo, A. P., de Assis, M. A., de Ferraz, S. M. F., Fiamenghi, M. B., José, J., Mofatto, L. S., Nagamatsu, S. T., Persinoti, G. F., et al. (2019) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2019.02.016 · Cited by 37 · see citing works
Harvesting of Microalgae for Biomass Production
Roselet, F., Vandamme, D., Muylaert, K., & Abreu, P. C. (2019) · Springer eBooks · doi:10.1007/978-981-13-2264-8_10 · Cited by 36 · see citing works
Dhokane, D., Bhadra, B., & Dasgupta, S. (2020) · Molecular Biology Reports · doi:10.1007/s11033-020-05922-5 · Cited by 37 · see citing works
Ma, C., Ren, H., Xing, D., Xie, G.-J., Ren, N., & Liu, B.-F. (2019) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2019.04.079 · Cited by 35 · see citing works
Chen, R., Yamaoka, Y., Feng, Y., Chi, Z., Xue, S., & Kong, F. (2023) · Metabolites · doi:10.3390/metabo13010115 · Cited by 35 · see citing works
Chen, R., Yang, M., Li, M., Zhang, H., Han, L., Dou, X., Feng, S., Xue, S., Zhu, C., Chi, Z., et al. (2022) · Biotechnology for Biofuels and Bioproducts · doi:10.1186/s13068-022-02154-6 · Cited by 34 · see citing works
Fields, F. J., Ostrand, J. T., Tran, M., & Mayfield, S. P. (2019) · Algal Research · doi:10.1016/j.algal.2019.101523 · Cited by 33 · see citing works
Self-citationAfifudeen, C. L. W., Loh, S. H., Ahmad, A., Takahashi, K., Effendy, A. W. M., & Cha, T. S. (2021) · Scientific Reports · doi:10.1038/s41598-020-79711-2 · Cited by 33 · see citing works
Hashiro, S., & Yasueda, H. (2022) · Applied Sciences · doi:10.3390/app12062954 · Cited by 32 · see citing works
MicroRNAs modulate adaption to multiple abiotic stresses in Chlamydomonas reinhardtii
Gao, X., Zhang, F., Hu, J., Cai, W., Shan, G., Dai, D., Huang, K., & Wang, G. (2016) · Scientific Reports · doi:10.1038/srep38228 · Cited by 32 · see citing works
Haire, T. C., Bell, C., Cutshaw, K., Swiger, B., Winkelmann, K., & Palmer, A. G. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00235 · Cited by 31 · see citing works
Shin, S.-E., Koh, H. G., Kang, N. K., Suh, W. I., Jeong, B., Lee, B., & Chang, Y. K. (2017) · Biotechnology for Biofuels · doi:10.1186/s13068-017-1000-0 · Cited by 31 · see citing works
Mora-Salguero, D., Fernández‐Niño, M., Serrano‐Bermúdez, L. M., Melo, D. O. P., Winck, F. V., Caldana, C., & Barrios, A. F. G. (2018) · PeerJ · doi:10.7717/peerj.5528 · Cited by 30 · see citing works
Payne, Z. L., Penny, G. M., Turner, T. N., & Dutcher, S. K. (2022) · Plant Communications · doi:10.1016/j.xplc.2022.100493 · Cited by 30 · see citing works
Singh, A., Singh, S., Singh, S., Prasad, N., & Asthana, R. K. (2024) · Renewable Energy · doi:10.1016/j.renene.2024.122256 · Cited by 28 · see citing works
Microalgae extracts: Potential anti-Trypanosoma cruzi agents?
Veas, R., Rojas-Pirela, M., Castillo, C., Olea‐Azar, C., Moncada‐Basualto, M., Ulloa, P. A., Rojas, V., & Kemmerling, U. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110178 · Cited by 29 · see citing works
Sproles, A. E., Berndt, A., Fields, F. J., & Mayfield, S. P. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-11790-9 · Cited by 28 · see citing works
Self-citationBeltran-Aguilar, A. G., Peraza-Echeverría, S., López-Ochoa, L., Borges-Argáez, I. C., & Herrera-Valencia, V. A. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09733-y · Cited by 27 · see citing works
An Insight into the Algal Evolution and Genomics
Khan, A. K., Kausar, H., Jaferi, S. S., Drouet, S., Hano, C., Abbasi, B., & Anjum, S. (2020) · Biomolecules · doi:10.3390/biom10111524 · Cited by 18 · see citing works
Recombinant Protein Stability in Cyanobacteria
Zhang, X., Betterle, N., Hidalgo, D., & Melis, A. (2021) · ACS Synthetic Biology · doi:10.1021/acssynbio.0c00610 · Cited by 27 · see citing works
Winck, F. V., Melo, D. O. P., Riaño‐Pachón, D. M., Martins, M. C. M., Caldana, C., & Barrios, A. F. G. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00043 · Cited by 27 · see citing works
Xu, L., Cheng, X., & Wang, Q. (2017) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2017.06.223 · Cited by 27 · see citing works
An Extended Approach to Quantify Triacylglycerol in Microalgae by Characteristic Fatty Acids
Yang, M., Fan, Y., Wu, P., Chu, Y., Shen, P., Xue, S., & Chi, Z. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01949 · Cited by 26 · see citing works
ElZorkany, H. E., Farghali, M. A., Hassan, M. A., El-Sayed, K., Canonico, M., Konert, G., Farroh, K. Y., Elshoky, H. A., & Kaňa, R. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.02.274 · Cited by 26 · see citing works
Craig, R. J., Böndel, K. B., Arakawa, K., Nakada, T., Ito, T., Bell, G., Colegrave, N., Keightley, P. D., & Ness, R. W. (2019) · Molecular Ecology · doi:10.1111/mec.15193 · Cited by 28 · see citing works
Giannakis, N., Carmona‐Cabello, M., Makri, A., Leiva-Candia, D. E., Filippi, K., Argeiti, C., Pateraki, C., Dorado, M. P., Koutinas, A., & Stylianou, E. (2023) · Renewable Energy · doi:10.1016/j.renene.2023.01.110 · Cited by 26 · see citing works
Romanchuk, L. D., Fedonuk, T. P., & Khant, G. O. (2017) · Regulatory Mechanisms in Biosystems · doi:10.15421/021770 · Cited by 26 · see citing works
Singh, A., Singh, S., Prasad, N., Singh, S., Mohanta, A., Kayastha, A. M., & Asthana, R. K. (2025) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2025.108015 · Cited by 26 · see citing works
Early Evolution of the Mitogen-Activated Protein Kinase Family in the Plant Kingdom
Kalapos, B., Hlavová, M., Nádai, T. V., Galiba, G., Bišová, K., & Dóczi, R. (2019) · Scientific Reports · doi:10.1038/s41598-019-40751-y · Cited by 25 · see citing works
Sandoval-Vargas, J. M., Jiménez-Clemente, L. A., Macedo-Osorio, K. S., Oliver-Salvador, M. C., Fernández-Linares, L. C., Durán‐Figueroa, N., & Badillo-Corona, J. A. (2019) · Molecular Biotechnology · doi:10.1007/s12033-019-00177-3 · Cited by 25 · see citing works
Chlamydomonas cell cycle mutant crcdc5 over-accumulates starch and oil
Torres-Romero, I., Kong, F., Légeret, B., Beisson, F., Peltier, G., & Li‐Beisson, Y. (2019) · Biochimie · doi:10.1016/j.biochi.2019.09.017 · Cited by 25 · see citing works
Muthulakshmi, C., Sivaranjani, R., & Selvi, S. (2021) · Biotechnology Reports · doi:10.1016/j.btre.2021.e00668 · Cited by 25 · see citing works
Singh, M., Mal, N., Mohapatra, R., Bagchi, T., Parambath, S. D., Chavali, M. S., Rao, K. M., Ramanaiah, S. V., Kadier, A., Kumar, G., et al. (2022) · Chemosphere · doi:10.1016/j.chemosphere.2022.133513 · Cited by 25 · see citing works
Rommelfanger, S. R., Zhou, M., Shaghasi, H., Tzeng, S., Evans, B. S., Paša‐Tolić, L., Umen, J., & Pesavento, J. J. (2021) · Journal of the American Society for Mass Spectrometry · doi:10.1021/jasms.1c00029 · Cited by 23 · see citing works
- Authors
- Scranton, M. A., Ostrand, J. T., Fields, F. J., & Mayfield, S. P.
- Affiliations
- University of California San Diego (US)
- Corresponding author
- Mayfield, Stephen P.
- Venue
- The Plant Journal
- Publisher
- Wiley
- Published
- 2015-02-18
- Volume
- 82
- Issue
- 3
- Pages
- 523-531
- ISSN
- 0960-7412 (ISSN-L)
- 1365-313X
- PMC
- PMC5531182
- OpenAlex
- W1967819652
- Cited by
- 267
- References
- 104
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 24 · 2023: 28 · 2022: 27 · 2021: 30 · 2020: 25 · 2019: 29 · 2018: 18 · 2017: 27 · 2016: 18 · 2015: 11
- FWCI
- 0.81
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- The Plant Journal (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- U.S. Department of Energy (DE‐EE0003373)
- California Energy Commission (CILMSF 500‐10‐039)
- Topics
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Algal biology and biofuel production
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
- Keywords
- Chlamydomonas reinhardtii, algae, biofuels, cellulosic ethanol, biodiesel, nutraceuticals, genetic engineering of algae, algal metabolism, renewable energy, strain improvement
- MeSH terms
- Biotechnology, Chlamydomonas, Chloroplasts, Genetic Engineering, Hydrogen, Chlamydomonas reinhardtii, Biofuels, High-Throughput Screening Assays, Microalgae, Homologous Recombination
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review