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Energy & Wetland Research Group, Centre for Ecological Sciences, Indian Institute of Science, Bangalore - 560012
CLASSIFICATION OF ALGAE
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Algae can be used as the feedstocks for the biodiesel because of its behavior of synthesizing and accumulating large amount of ALGAE
lipids , high growth rates, tolerance to very adverse conditions, production of value adding products.
Algal population can be affected by the environmental factors like seasonal changes, nutrient availability , light penetration etc.
Algae are primarily made up of proteins carbohydrates, fats and lipids in varying proportions.
They can accumulate large amount of protein about 47% of total biomass. Cyanophyta Chlorophyta Cryptophyta Bacillariophyta Haptophyta Dinophyta Eustigmatophyta
In algae the organic carbon is represented by carbohydrates, polysaccharides , nitrogenous and polyphenolic materials .
The diversity of algal lipids and its ability to modify the lipid composition according to environment made them ubiquitous.
References
Fatty acid Bacillariophyta Eustigmatophyta Chlorophyta Haptophyta Cyanophyta Cryptophyta Dinophyta C16:0 C18:1 C18:1 C18:1 C18:2 C18:1 C16:0 C18:0 C18:0 C16:1 C20:1
C18:0 C18:1 C16:0 C18:1 C18:1 C16:0 C16:0 C18:1 C16:0 C18:1 C18:1 Ben-Amotz, A., Shaish, A. and Avron, M. (1989) Mode of action of the
C10:0 + massively accumulated b-carotene of Dunaliella bardawil in protecting the
C16:0 C18:1 C18:1 C18:1 C18:0 C18:1 C18:0 C18:2 C18:1 C16:0 C18:0 alga against damage by excess irradiation. Plant Physiol. 91, 1040–1043.
C11:0 +
C16:1ω9 + + +
Guckert, J.B. and Cooksey, K.E. (1990) Triacylglyceride accumulation and
fatty acid changes in Chlorella (Chlorophyta) during high-pH induced cell
C16:2ω4 + + + cycle inhibition. J. Phycol. 26, 72–79.
C18:0 + + + + + +
The lipid classes are present in all the algal species are C16:0, C16:1ω7, C18:1ω9, C18:3ω3, Kathen, M. (1949) U¨ ber die Ermittelung der chemischen Konstitution von
C18:3ω6. Algenlipoiden mit Hilfe der Adsorptionsmethode. Arch.Mikrobiol. 14, 602–
C18:1ω7 + + + 634.
C18:1ω9 + + + + + + + They have the ability to produce TAG as a storage lipid under photo-oxidative stress or Lee, R.F. and Loeblich, A.R. III (1971) Distribution of 21:6 hydrocarbon
other adverse environmental conditions. and its relationship to 22:6 fatty acid in algae. Phytochemistry, 10, 593–602.
C18:1ω13 +
C18:2ω6 + + + + + + Chlorophyta, Bacillariophyta and Cyanobacteria are the most favored algae by the Lynch, D.V. and Thompson, G.A. (1982) Low temperature-
inducedalterations in the chloroplast and microsomal membranes of
C18:3ω3 + + + + + + +
researcher for biofuels production due to their high lipid content. Dunaliella salina. Plant Physiol. 69, 1369–1375.
C18:3ω6 + + + + + + + Some of these unsaturated fatty acids that are found in different algal species include: Mansour, M.P., Volkman, J.K. and Blackburn, S.I. (2003) The effect of
growth phase on the lipid class, fatty acid and sterol composition in the
C18:4ω3 + + + + + + arachidonic acid, eicospentaenoic acid, docasahexaenoic acid, gamma-linolenic acid, and
marine dinoflagellate, Gymnodinium sp. in batch culture. Phytochemistry,
linoleic acid. 63, 145–153
C18:5ω3 + +
C20:0 + TAGs are the Microalgal feedstock of Biodiesel production and PUFAs provides essential Ohlrogge, J. and Browse, J. (1995) Lipid biosynthesis. Plant Cell, 7, 957–
970.
fatty acids.
C20:1 +
Roessler, P.G. (1987) UDP-glucose pyrophosphorylase activity in the
C20:4ω6 + + + Shift in lipid metabolism from membrane lipid synthesis to the storage of neutral lipids diatom Cyclotella cryptica: pathway of chrysolaminarin biosynthesis. J.
takes place in adverse situation. Phycol. 23, 494–498.
C20:5ω3 + + + + +
C22:5ω3 + +
Acknowledgement
C22:6ω3 + +
I want to thank entire EWRG for their valuable suggestions.
C24:0 +
Source LAKE 2010: WETLANDS, BIODIVERSITY AND CLIMATE
Table : showing the fatty acids present in different algae CHANGE