Microalgae–bacteria symbiosis in microalgal growth and biofuel production: A review
Open accessAbstract
Photosynthetic microalgae can capture solar energy and convert it to bioenergy and biochemical products. In nature or industrial processes, microalgae live together with bacterial communities and may maintain symbiotic relationships. In general interactions, microalgae exude dissolved organic carbon that becomes available to bacteria. In return, the bacteria remineralize sulphur, nitrogen and phosphorous to support the further growth of microalgae. In specific interactions, heterotrophic bacteria supply B vitamins as organic cofactors or produce siderophores to bind iron, which could be utilized by microalgae, while the algae supply fixed carbon to the bacteria in return. In this review, we focus on mutualistic relationship between microalgae and bacteria, summarizing recent studies on the mechanisms involved in microalgae-bacteria symbiosis. Symbiotic bacteria on promoting microalgal growth are described and the relevance of microalgae-bacteria interactions for biofuel production processes is discussed. Symbiotic microalgae-bacteria consortia could be utilized to improve microalgal biomass production and to enrich the biomass with valuable chemical and energy compounds. The suitable control of such biological interactions between microalgae and bacteria will help to improve the microalgae-based biomass and biofuel production in the future.
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?
Microalgae-bacteria consortia have been explored as an alternative route to enhancing microalgae growth and metabolite production because growth-promoting factors are produced by bacteria.
“Since these growth-promoting factors are produced by bacteria, microalgae–bacteria consortia have been explored as an alternative route to enhancing microalgae growth and metabolite production [9,10].”
From Toward the Enhancement of Microalgal Metabolite Production through Microalgae–Bacteria Consortia (2021) · cites this paper as [9]
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
Chisti, Y. (2007) · Biotechnology Advances · doi:10.1016/j.biotechadv.2007.02.001 · Cited by 9,524 · see citing works
The Evolution and Future of Earth’s Nitrogen Cycle
Canfield, D. E., Glazer, A. N., & Falkowski, P. G. (2010) · Science · doi:10.1126/science.1186120 · Cited by 2,697 · see citing works
Microbial structuring of marine ecosystems
Azam, F., & Malfatti, F. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1747 · Cited by 1,705 · see citing works
Algae acquire vitamin B12 through a symbiotic relationship with bacteria
Croft, M. T., Lawrence, A. D., Raux-Deery, E., Warren, M. J., & Smith, A. G. (2005) · Nature · doi:10.1038/nature04056 · Cited by 1,536 · see citing works
Algal–bacterial processes for the treatment of hazardous contaminants: A review
Muñoz, R., & Guieysse, B. (2006) · Water Research · doi:10.1016/j.watres.2006.06.011 · Cited by 1,497 · see citing works
Algae-bacteria interactions: Evolution, ecology and emerging applications
Ramanan, R., Kim, B.-H., Cho, D.-H., Oh, H.-M., & Kim, H.-S. (2016) · Biotechnology Advances · doi:10.1016/j.biotechadv.2015.12.003 · Cited by 1,301 · see citing works
Master recyclers: features and functions of bacteria associated with phytoplankton blooms
Buchan, A., LeCleir, G. R., Gulvik, C. A., & González, J. M. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3326 · Cited by 1,212 · see citing works
Anaerobic digestion of microalgae as a necessary step to make microalgal biodiesel sustainable
Sialve, B., Bernet, N., & Bernard, O. (2009) · Biotechnology Advances · doi:10.1016/j.biotechadv.2009.03.001 · Cited by 1,187 · see citing works
Biodiesel from algae: challenges and prospects
Scott, S. A., Davey, M. P., Dennis, J. S., Horst, I., Howe, C. J., Lea-Smith, D. J., & Smith, A. G. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.03.005 · Cited by 1,183 · see citing works
Assessment of the anaerobic biodegradability of macropollutants
Angelidaki, İ., & Sanders, W. T. M. (2004) · Reviews in Environmental Science and Bio/Technology · doi:10.1007/s11157-004-2502-3 · Cited by 1,136 · see citing works
Increase in Chlorella strains calorific values when grown in low nitrogen medium
Illman, A. M., Scragg, A. H., & Shales, S. W. (2000) · Enzyme and Microbial Technology · doi:10.1016/s0141-0229(00)00266-0 · Cited by 1,008 · see citing works
Interactions between Diatoms and Bacteria
Amin, S., Parker, M., & Armbrust, E. (2012) · Microbiology and Molecular Reviews · doi:10.1128/mmbr.00007-12 · Cited by 894 · see citing works
Interactions Between Bacteria and Algae in Aquatic Ecosystems
Cole, J. J. (1982) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.es.13.110182.001451 · Cited by 768 · see citing works
Constraints to Commercialization of Algal Fuels
Chisti, Y. (2013) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2013.07.020 · Cited by 719 · see citing works
(2013) · doi:10.1007/978-94-007-5479-9 · Cited by 670 · see citing works
HANDBOOK OF MICROALGAL CULTURE: BIOTECHNOLOGY AND APPLIED PHYCOLOGY
Henry, E. C. (2004) · Journal of Phycology · doi:10.1111/j.1529-8817.2004.40502.x · Cited by 655 · see citing works
Hydrogen Production. Green Algae as a Source of Energy
Melis, A., & Happe, T. (2001) · Plant Physiology · doi:10.1104/pp.010498 · Cited by 655 · see citing works
Opportunities for renewable bioenergy using microorganisms
Rittmann, B. E. (2008) · Biotechnology and Bioengineering · doi:10.1002/bit.21875 · Cited by 651 · see citing works
Photolysis of iron–siderophore chelates promotes bacterial–algal mutualism
Amin, S. A., Green, D. H., Hart, M. C., Küpper, F. C., Sunda, W. G., & Carrano, C. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905512106 · Cited by 583 · see citing works
Marine diatom species harbour distinct bacterial communities
Grossart, H., Levold, F., Allgaier, M., Simon, M., & Brinkhoff, T. (2005) · Environmental Microbiology · doi:10.1111/j.1462-2920.2005.00759.x · Cited by 547 · see citing works
Unicellular Cyanobacterium Symbiotic with a Single-Celled Eukaryotic Alga
Thompson, A., Foster, R. A., Krupke, A., Carter, B. J., Musat, N., Vaulot, D., Kuypers, M. M. M., & Zehr, J. P. (2012) · Science · doi:10.1126/science.1222700 · Cited by 518 · see citing works
Consortia of cyanobacteria/microalgae and bacteria: Biotechnological potential
Subashchandrabose, S. R., Ramakrishnan, B., Megharaj, M., Venkateswarlu, K., & Naidu, R. (2011) · Biotechnology Advances · doi:10.1016/j.biotechadv.2011.07.009 · Cited by 492 · see citing works
Fuentes, J., Garbayo, I., Cuaresma, M., Montero, Z., González-del-Valle, M., & Vílchez, C. (2016) · Marine Drugs · doi:10.3390/md14050100 · Cited by 462 · see citing works
Engineering algae for biohydrogen and biofuel production
Beer, L. L., Boyd, E. S., Peters, J. W., & Posewitz, M. C. (2009) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2009.06.002 · Cited by 449 · see citing works
Kazamia, E., Czesnick, H., Nguyen, T. T. V., Croft, M. T., Sherwood, E., Sasso, S., Hodson, S. J., Warren, M. J., & Smith, A. G. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02733.x · Cited by 410 · see citing works
Nitrogen fixation and transfer in open ocean diatom–cyanobacterial symbioses
Foster, R. A., Kuypers, M. M. M., Vágner, T., Paerl, R. W., Musat, N., & Zehr, J. P. (2011) · The ISME Journal · doi:10.1038/ismej.2011.26 · Cited by 409 · see citing works
Chemistry of Marine Ligands and Siderophores
Gauglitz, J. M., & Butler, A. (2008) · Annual Review of Marine Science · doi:10.1146/annurev.marine.010908.163712 · Cited by 358 · see citing works
Bacterial Taxa That Limit Sulfur Flux from the Ocean
Howard, E. C., Henriksen, J. R., Buchan, A., Reisch, C. R., Bürgmann, H., Welsh, R. M., Ye, W., González, J. M., Mace, K., Joye, S. B., et al. (2006) · Science · doi:10.1126/science.1130657 · Cited by 345 · see citing works
Griffiths, M. J., van Hille, R. P., & Harrison, S. T. L. (2012) · Journal of Applied Phycology · doi:10.1007/s10811-011-9723-y · Cited by 341 · see citing works
Bioethanol from microalgae and cyanobacteria: A review and technological outlook
Silva, C. E. D. F., & Bertucco, A. (2016) · Process Biochemistry · doi:10.1016/j.procbio.2016.02.016 · Cited by 309 · see citing works
Microalgae-Based Biofuels and Bioproducts
Gonzalez-Fernandez, C., & Muñoz, R. (2017) · Elsevier eBooks · doi:10.1016/c2015-0-05935-4 · Cited by 306 · see citing works
Species-Specific Bacterial Communities in the Phycosphere of Microalgae?
Sapp, M., Schwaderer, A. S., Wiltshire, K. H., Hoppe, H., Gerdts, G., & Wichels, A. (2007) · Microbial Ecology · doi:10.1007/s00248-006-9162-5 · Cited by 277 · see citing works
Most harmful algal bloom species are vitamin B 1 and B 12 auxotrophs
Tang, Y. Z., Koch, F., & Gobler, C. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009566107 · Cited by 272 · see citing works
Brinkhoff, T., Bach, G., Heidorn, T., et al. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.4.2560-2565.2003 · Cited by 239 · see citing works
Characterization of extracellular polymeric substances produced by micro-algae Dunaliella salina
Mishra, A., Kavita, K., & Jha, B. (2010) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2010.08.067 · Cited by 220 · see citing works
Marine bacteria and biogeochemical cycling of iron in the oceans
Tortell, P. D., Maldonado, M. T., Granger, J., & Price, N. M. (1999) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.1999.tb00593.x · Cited by 206 · see citing works
The role of siderophores in iron acquisition by photosynthetic marine microorganisms
Hopkinson, B. M., & Morel, F. M. M. (2009) · BioMetals · doi:10.1007/s10534-009-9235-2 · Cited by 196 · see citing works
He, Z., Kan, J., Mansfeld, F. B., et al. (2009) · Environmental Science & Technology · doi:10.1021/es803084a · Cited by 194 · see citing works
Bruckner, C. G., Rehm, C., Grossart, H., & Kroth, P. G. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2010.02411.x · Cited by 181 · see citing works
Molecular mechanisms underlying roseobacter–phytoplankton symbioses
Geng, H., & Belas, R. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.03.013 · Cited by 173 · see citing works
SEQUENCE ANALYSIS AND TRANSCRIPTIONAL REGULATION OF IRON ACQUISITION GENES IN TWO MARINE DIATOMS1
Kustka, A. B., Allen, A. E., & Morel, F. M. M. (2007) · Journal of Phycology · doi:10.1111/j.1529-8817.2007.00359.x · Cited by 168 · see citing works
Bacterial community associated with Pfiesteria ‐like dinoflagellate cultures
Alavi, M., Miller, T. R., Erlandson, K. A., et al. (2001) · Environmental Microbiology · doi:10.1046/j.1462-2920.2001.00207.x · Cited by 161 · see citing works
Roseobacticides: Small Molecule Modulators of an Algal-Bacterial Symbiosis
Seyedsayamdost, M. R., Carr, G., Kolter, R., et al. (2011) · Journal of the American Chemical Society · doi:10.1021/ja207172s · Cited by 152 · see citing works
Park, Y., Je, K.-W., Lee, K., Jung, S.-E., & Choi, T.-J. (2008) · Hydrobiologia · doi:10.1007/s10750-007-9152-8 · Cited by 150 · see citing works
Screening and selection of growth-promoting bacteria for Dunaliella cultures
Chevanton, M. L., Garnier, M., Bougaran, G., Schreiber, N., Lukomska, E., Bérard, J., Fouilland, É., Olivier Bernard, A., & Cadoret, J. (2013) · Algal Research · doi:10.1016/j.algal.2013.05.003 · Cited by 147 · see citing works
Vitamins, phytoplankton and bacteria: symbiosis or scavenging?
Droop, M. R. (2007) · Journal of Plankton Research · doi:10.1093/plankt/fbm009 · Cited by 127 · see citing works
Guo, Z. M., & Tong, Y. W. (2013) · Journal of Applied Phycology · doi:10.1007/s10811-013-0186-1 · Cited by 127 · see citing works
Use of Cellulolytic Marine Bacteria for Enzymatic Pretreatment in Microalgal Biogas Production
Muñoz, C. F., Hidalgo, C., Zapata, M., Jeison, D., Riquelme, C. E., & Rivas, M. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.00827-14 · Cited by 114 · see citing works
Saccharification of Marine Microalgae Using Marine Bacteria for Ethanol Production
Matsumoto, M., Yokouchi, H., Suzuki, N., Ohata, H., & Matsunaga, T. (2003) · Applied Biochemistry and Biotechnology · doi:10.1385/abab:105:1-3:247 · Cited by 111 · see citing works
Bacterial bioaugmentation for improving methane and hydrogen production from microalgae
Lü, F., Jiaqi, J., Shao, L., & He, P. (2013) · Biotechnology for Biofuels · doi:10.1186/1754-6834-6-92 · Cited by 110 · see citing works
A complex iron-calcium cofactor catalyzing phosphotransfer chemistry
Yong, S. C., Roversi, P., Lillington, J., et al. (2014) · Science · doi:10.1126/science.1254237 · Cited by 104 · see citing works
Cruz‐López, R., & Maske, H. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00560 · Cited by 104 · see citing works
Stimulation of Alexandrium fundyense growth by bacterial assemblages from the Bay of Fundy
Ferrier, M., Martin, J. L., & Rooney‐Varga, J. N. (2002) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2002.01576.x · Cited by 102 · see citing works
Microalgal symbiosis in biotechnology
Santos, C. A., & dos Reis, A. J. D. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-5764-x · Cited by 96 · see citing works
Bacterial symbionts enhance photo-fermentative hydrogen evolution of Chlamydomonas algae
Lakatos, G., Deák, Z., Vass, I., Rétfalvi, T., Rozgonyi, S., Rákhely, G., Ördög, V., Kondorosi, É., & Maróti, G. (2014) · Green Chem. · doi:10.1039/c4gc00745j · Cited by 95 · see citing works
Oligotrophic bacteria enhance algal growth under iron-deficient conditions
Keshtacher-Liebso, E., Hadar, Y., & Chen, Y. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.6.2439-2441.1995 · Cited by 93 · see citing works
Higgins, B. T., & VanderGheynst, J. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096807 · Cited by 89 · see citing works
Cofactor symbiosis for enhanced algal growth, biofuel production, and wastewater treatment
Higgins, B. T., Gennity, I., Samra, S., Kind, T., Fiehn, O., & VanderGheynst, J. S. (2016) · Algal Research · doi:10.1016/j.algal.2016.05.024 · Cited by 66 · see citing works
Marine Cyanobacterial Symbioses
Carpenter, E. J., & Foster, R. A. (2005) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-48005-0_2 · Cited by 63 · see citing works
Detection of glycolate oxidase gene glcD diversity among cultured and environmental marine bacteria
Lau, W. W. Y., & Armbrust, E. V. (2006) · Environmental Microbiology · doi:10.1111/j.1462-2920.2006.01092.x · Cited by 59 · see citing works
Cellular interactions: lessons from the nitrogen‐fixing cyanobacteria
Thompson, A., & Zehr, J. P. (2013) · Journal of Phycology · doi:10.1111/jpy.12117 · Cited by 59 · see citing works
Park, J., Park, B. S., Wang, P., Patidar, S. K., Kim, J. H., Kim, S.-H., & Han, M. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00289 · Cited by 58 · see citing works
Zhu, L. (2013) · Biofuels Bioproducts and Biorefining · doi:10.1002/bbb.1442 · Cited by 55 · see citing works
Bell, T. A. S., Prithiviraj, B., Wahlen, B. D., Fields, M. W., & Peyton, B. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01480 · Cited by 47 · see citing works
Amin, S. A., Green, D. H., Gärdes, A., Romano, A., Trimble, L., & Carrano, C. J. (2011) · BioMetals · doi:10.1007/s10534-011-9495-5 · Cited by 39 · see citing works
Microorganisms and clean energy
Donohue, T. J., & Cogdell, R. J. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1534 · Cited by 35 · see citing works
New Pieces for the Marine Sulfur Cycle Jigsaw
Malin, G. (2006) · Science · doi:10.1126/science.1133279 · Cited by 28 · see citing works
Strategies for Bioprospecting Microalgae for Potential Commercial Applications
Barclay, W., & Apt, K. E. (2013) · doi:10.1002/9781118567166.ch4 · Cited by 27 · see citing works
Ruttenberg, K. C. (2001) · Elsevier eBooks · doi:10.1016/b978-012374473-9.00277-0 · Cited by 9 · see citing works
Baggesen, C. (2014) · Cited by 6 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Illman, A.M., Scragg, A.H., Shales, S.W. (2000) Increase in Chlorella nitrogen medium. Enzyme Microb Technol 27(8) :631-635.
Cited by
Sorted by citations
Advanced microalgae-based renewable biohydrogen production systems: A review
Goswami, R. K., Mehariya, S., Obulisamy, P. K., & Verma, P. (2021) · Bioresource Technology · doi:10.1016/j.biortech.2020.124301 · Cited by 189 · see citing works
A review on co-culturing of microalgae: a greener strategy towards sustainable biofuels production
Ray, A., Nayak, M., & Ghosh, A. (2022) · Science of The Total Environment · doi:10.1016/j.scitotenv.2021.149765 · Cited by 168 · see citing works
Toward the Enhancement of Microalgal Metabolite Production through Microalgae–Bacteria Consortia
González-González, L. M., & de-Bashan, L. E. (2021) · Biology · doi:10.3390/biology10040282 · Cited by 133 · see citing works
Ferrando, L., & Matamoros, V. (2020) · Science of The Total Environment · doi:10.1016/j.scitotenv.2019.134740 · Cited by 98 · see citing works
Lian, J., Schimmel, P., Sanchez‐Garcia, S., Wijffels, R. H., Smidt, H., & Sipkema, D. (2021) · Microbial Biotechnology · doi:10.1111/1751-7915.13784 · Cited by 34 · see citing works
Daly, G., Ghini, V., Adessi, A., Fondi, M., Buchan, A., & Viti, C. (2022) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuac020 · Cited by 30 · see citing works
Iakovidou, G., Itziou, A., Tsiotsias, A., Lakioti, E., Samaras, P., Tsanaktsidis, C., & Karayannis, V. (2024) · Applied Sciences · doi:10.3390/app14156727 · Cited by 29 · see citing works
Saputri, D. A. E., Prabaningtyas, S., & Aridowi, D. (2025) · AIP Conference Proceedings · doi:10.1063/5.0234821 · Cited by 1 · see citing works
- Authors
- Yao, S., Lyu, S., An, Y., Lu, J., Gjermansen, C., & Schramm, A.
- Affiliations
- Shenyang Agricultural University (CN)
- Technical University of Denmark (DK)
- Aarhus University (DK)
- Corresponding author
- An, Y.
- Venue
- Journal of Applied Microbiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2018-10-03
- Volume
- 126
- Issue
- 2
- Pages
- 359-368
- ISSN
- 1364-5072 (ISSN-L)
- OpenAlex
- W2889405956
- Cited by
- 296
- References
- 70
- Citations by year
- 2026: 23 · 2025: 42 · 2024: 47 · 2023: 59 · 2022: 50 · 2021: 42 · 2020: 22 · 2019: 10 · 2018: 1
- FWCI
- 1.01
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Applied Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Technical University of Denmark, DTU Orbit (Technical University of Denmark, DTU) (submittedVersion, other-oa)
- Funders
- Shenyang Agricultural University
- 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
- Physical Sciences › Environmental Science › Environmental Chemistry › Aquatic Ecosystems and Phytoplankton Dynamics
- Keywords
- microalgae-bacteria symbiosis, mutualism, microalgae growth, biofuel production, nutrient remineralization, siderophores, B vitamins, heterotrophic bacteria, microalgal biomass, photosynthetic microalgae
- MeSH terms
- Bacteria, Symbiosis, Biomass, Heterotrophic Processes, Biofuels, Microalgae
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