Microalgae Explained

Microalgae or microphytes are microscopic algae invisible to the naked eye. They are phytoplankton typically found in freshwater and marine systems, living in both the water column and sediment. They are unicellular species which exist individually, or in chains or groups. Depending on the species, their sizes can range from a few micrometers (μm) to a few hundred micrometers. Unlike higher plants, microalgae do not have roots, stems, or leaves. They are specially adapted to an environment dominated by viscous forces.

Microalgae, capable of performing photosynthesis, are important for life on earth; they produce approximately half of the atmospheric oxygen[1] and use the greenhouse gas carbon dioxide to grow photoautotrophically. "Marine photosynthesis is dominated by microalgae, which together with cyanobacteria, are collectively called phytoplankton."[2] Microalgae, together with bacteria, form the base of the food web and provide energy for all the trophic levels above them. Microalgae biomass is often measured with chlorophyll a concentrations and can provide a useful index of potential production.[3] [4]

The biodiversity of microalgae is enormous and they represent an almost untapped resource. It has been estimated that about 200,000-800,000 species in many different genera exist of which about 50,000 species are described.[5] Over 15,000 novel compounds originating from algal biomass have been chemically determined. Examples include carotenoids, antioxidants, fatty acids, enzymes, polymers, peptides, toxins and sterols.[6] Besides providing these valuable metabolites, microalgae is regarded as a potential feedstock for biofuels and has also emerged as a promising microorganism in bioremediation.[7]

An exception to the microalgae family is the colorless Prototheca which are devoid of any chlorophyll. These achlorophic algae switch to parasitism and thus cause the disease protothecosis in human and animals.

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Characteristics and uses

The chemical composition of microalgae is not an intrinsic constant factor but varies over a wide range of factors, both depending on species and on cultivation conditions. Some microalgae have the capacity to acclimate to changes in environmental conditions by altering their chemical composition in response to environmental variability. A particularly dramatic example is their ability to replace phospholipids with non-phosphorus membrane lipids in phosphorus-depleted environments.[8] It is possible to accumulate the desired products in microalgae to a large extent by changing environmental factors, like temperature, illumination, pH, CO2 supply, salt and nutrients.

Microphytes also produce chemical signals which contribute to prey selection, defense, and avoidance. These chemical signals affect large scale tropic structures such as algal blooms but propagate by simple diffusion and laminar advective flow.[9] Microalgae such as microphytes constitute the basic foodstuff for numerous aquaculture species, especially filtering bivalves.

Photo- and chemosynthetic algae

Photosynthetic and chemosynthetic microbes can also form symbiotic relationships with host organisms. They provide them with vitamins and polyunsaturated fatty acids, necessary for the growth of the bivalves which are unable to synthesize it themselves. In addition, because the cells grow in aqueous suspension, they have more efficient access to water, CO2, and other nutrients.

Microalgae play a major role in nutrient cycling and fixing inorganic carbon into organic molecules and expressing oxygen in marine biosphere.

While fish oil has become famous for its omega-3 fatty acid content, fish do not actually produce omega-3s, instead accumulating their omega-3 reserves by consuming microalgae. These omega-3 fatty acids can be obtained in the human diet directly from the microalgae that produce them.

Microalgae can accumulate considerable amounts of proteins depending on species and cultivation conditions. Due to their ability to grow on non-arable land microalgae may provide an alternative protein source for human consumption or animal feed.[10] Microalgae proteins are also investigated as thickening agents[11] or emulsion and foam stabilizers[12] in the food industry to replace animal based proteins.

Some microalgae accumulate chromophores like chlorophyll, carotenoids, or phycobiliproteins that may be extracted and used as coloring agents.[13]

Cultivation of microalgae

See main article: article and Culture of microalgae in hatcheries. A range of microalgae species are produced in hatcheries and are used in a variety of ways for commercial purposes, including for human nutrition,[14] as biofuel,[15] in the aquaculture of other organisms,[16] in the manufacture of pharmaceuticals and cosmetics,[17] and as biofertiliser.[18] However, the low cell density is a major bottleneck in commercial viability of many microalgae derived products, especially low cost commodities.[19]

Studies have investigated the main factors in the success of a microalgae hatchery system to be:[20] [21]

See also

Notes and References

  1. Web site: Microscopic algae produce half the oxygen we breathe. 25 October 2013. ABC. Williams. Robyn. The Science Show. Robyn Williams. 11 November 2020.
  2. Parker . Micaela S. . Mock . Thomas . Armbrust . E. Virginia . 2008 . Genomic Insights into Marine Microalgae . . 42 . 619–645 . 10.1146/annurev.genet.42.110807.091417 . 18983264.
  3. Thrush. Simon. Hewitt. Judi. Judi Hewitt. Gibbs. Max. Lundquist. Caralyn. Norkko. Alf. 2006. Functional Role of Large Organisms in Intertidal Communities: Community Effects and Ecosystem Function. Ecosystems. 9. 6. 1029–1040. 10.1007/s10021-005-0068-8. 23502276.
  4. Sun . Ning . Skaggs . Richard L. . Wigmosta . Mark S. . Coleman . André M. . Huesemann . Michael H. . Edmundson . Scott J. . July 2020 . Growth modeling to evaluate alternative cultivation strategies to enhance national microalgal biomass production . Algal Research . 49 . 101939 . 10.1016/j.algal.2020.101939 . 219431866 . 2211-9264. free .
  5. Starckx, Senne (31 October 2012) A place in the sun - Algae is the crop of the future, according to researchers in Geel Flanders Today, Retrieved 8 December 2012
  6. Ratha SK, Prasanna R . Bioprospecting microalgae as potential sources of "Green Energy"—challenges and perspectives . Applied Biochemistry and Microbiology . 48 . 2 . 109–125 . February 2012 . 22586907 . 10.1134/S000368381202010X. 18430041 .
  7. Book: Yuvraj . Microalgal Bioremediation: A Clean and Sustainable Approach for Controlling Environmental Pollution. 2022 . 1. 305–318. Innovations in Environmental Biotechnology. Singapore. Springer Singapore. en. 10.1007/978-981-16-4445-0_13. 978-981-16-4445-0 .
  8. Bonachela. Juan. Raghib. Michael. Levin. Simon. Dynamic model of flexible phytoplankton nutrient uptake. PNAS. Feb 21, 2012. 108. 51. 20633–20638. 10.1073/pnas.1118012108. 22143781. 3251133. free.
  9. Wolfe . Gordon . 2000 . The chemical Defense Ecology o Marine Unicelular Plankton: Constraints, Mechanisms, and Impacts . . 198 . 2 . 225–244 . 10.1.1.317.7878 . 10.2307/1542526 . 1542526 . 10786943.
  10. Becker . E. W. . Micro-algae as a source of protein . Biotechnology Advances . 1 March 2007 . 25 . 2 . 207–210 . 10.1016/j.biotechadv.2006.11.002 . 17196357 .
  11. Grossmann . Lutz . Hinrichs . Jörg . Weiss . Jochen . Cultivation and downstream processing of microalgae and cyanobacteria to generate protein-based technofunctional food ingredients . Critical Reviews in Food Science and Nutrition . 24 September 2020 . 60 . 17 . 2961–2989 . 10.1080/10408398.2019.1672137 . 31595777 . 203985553 .
  12. Bertsch . Pascal . Böcker . Lukas . Mathys . Alexander . Fischer . Peter . Proteins from microalgae for the stabilization of fluid interfaces, emulsions, and foams . Trends in Food Science & Technology . February 2021 . 108 . 326–342 . 10.1016/j.tifs.2020.12.014 . free . 20.500.11850/458592 . free .
  13. Hu . Jianjun . Nagarajan . Dillirani . Zhang . Quanguo . Chang . Jo-Shu . Lee . Duu-Jong . Heterotrophic cultivation of microalgae for pigment production: A review . Biotechnology Advances . January 2018 . 36 . 1 . 54–67 . 10.1016/j.biotechadv.2017.09.009 . 28947090 .
  14. Web site: Leckie . Evelyn . Adelaide scientists turn marine microalgae into 'superfoods' to substitute animal proteins . ABC News . . 14 Jan 2021 . 17 Jan 2021.
  15. Yusuf . Chisti . 2008 . Biodiesel from microalgae beats bioethanol . . 26 . 3 . 126–131 . 18221809 . 10.1016/j.tibtech.2007.12.002 .
  16. Arnaud Muller-Feuga . 2000 . The role of microalgae in aquaculture: situation and trends . Journal of Applied Phycology . 12 . 3 . 527–534 . 10.1023/A:1008106304417 . 8495961 .
  17. Isuru Wijesekara . Ratih Pangestuti . Se-Kwon Kim . 2010 . Biological activities and potential health benefits of sulfated polysaccharides derived from marine algae . Carbohydrate Polymers . 84 . 1 . 14–21 . 10.1016/j.carbpol.2010.10.062.
  18. Upasana Mishra . Sunil Pabbi . 2004 . Cyanobacteria: a potential biofertilizer for rice . Resonance . 9 . 6 . 6–10 . 10.1007/BF02839213 . 121561783 .
  19. Yuvraj . Ambarish Sharan Vidyarthi . Jeeoot Singh . 2016 . Enhancement of Chlorella vulgaris cell density: Shake flask and bench-top photobioreactor studies to identify and control limiting factors . Korean Journal of Chemical Engineering . 33 . 8 . 2396–2405 . 10.1007/s11814-016-0087-5 . 99110136 . subscription .
  20. Yuvraj . Padmini Padmanabhan . 2017 . Technical insight on the requirements for -saturated growth of microalgae in photobioreactors . 3 Biotech . 07 . 2 . 119 . 10.1007/s13205-017-0778-6 . 28567633 . 5451369 .
  21. Yuvraj . Ambarish Sharan Vidyarthi . Jeeoot Singh . 2016 . Enhancement of Chlorella vulgaris cell density: Shake flask and bench-top photobioreactor studies to identify and control limiting factors . Korean Journal of Chemical Engineering . 33 . 8 . 2396–2405 . 10.1007/s11814-016-0087-5 . 99110136 . subscription .