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Name derivation:

 

 

Classification:

Chlorella  M.Beijerinck  1890

Order Chlorellales;  Family Chlorellaceae;  33 of 96 species descriptions are currently accepted taxonomically (Guiry and Guiry).

Synonym:  Muriella.

 

Morphology:

Green spherical to ellipsoidal unicells with one chloroplast, often growing in groups.  Asexual reproduction by forming 2- 8 autospores.

 

Similar genera:

More than 100 taxa (probably species descriptions) have been incorrectly designated Chlorella (Krienitz et al. 2014).

 

Calvin cycle:

Dark (light-independent) reactions of PS use 9 ATP (fuel) and 6 NADPH (reducing power) molecules to incorporate 3 CO2 molecules into a single precursor of sugars: glyceraldehyde 3-phosphate.  Light reactions of PS produce the ATP and NADPH.  The cycle was determined with Chlorella cultures (Calvin and Benson 1948).

 

Biofuel potential:

High lipid content and growth rate are a major considerations for selecting microalgal strains.  Of five Chlorella species, C. emersonii growing in culture without a source of nitrogen (none was listed for the ‘low-N’ freshwater growth medium) had ~63% lipid content compared to the control culture grown in Watanbe medium (Watanabe 1960) with 1.25 g KNO3 L-1.  Although the initial growth rate was depressed (days 1-5) it then increased providing the highest yield after one week.  The protein content in N-limited culture was decreased (Illman et al. 2000).

 

Biogas wastewater utilization:

A model of biomethane production using the cyanobactium Spirulina predicted a net energy ratio of 1.54 using an existing biogas plant (Wang et al. 2013), suggesting the value of integrating microalgal production with biogas waste.

A test of using industrial wastewater is addition of biogas production wastewater containing 75-80% pure glycerol with methanol, free fatty acids, a catalyst residue and other impurities, added to BG11 medium minus nitrogen that supported mixotrophic growth.  Optimal growth was in the growth medium with 0.114 g L-1 N and 2.7 g L-1 technical glycerol (Skorupskaite et al. 2015).

 

Dairy wastewater utilization:

Chlorella sp. developed 23% lipids in ten days when grown on 80% dairy wastewater and 20% BG11 medium (Guruvaiah et al. 2012).

 

Health food competitor of Spirulina:

Mass culture of Chlorella is also targeting the health food industry with claims of body detoxification, greater longevity and antioxidants (β-carotene).

Habitat:

All aquatic habitats and wet subaerial surfaces.

 

 

References:

Beyerinck [Beijerinck], M.W.  1890.  Culturversuche mit Zoochlorellen, Lichenengonidien und anderen niederen Algen.  Botanische Zeitung 47: 725-739, 741-754, 757-768, 781-785.

Calvin, M. and A.A. Benson  1948.  The path of carbon in photosynthesis.  Science 107:476-480.

Guiry, M.D. and Guiry, G.M.  2013.  AlgaeBase. World-wide electronic publication, National University of Ireland, Galway.  http://www.algaebase.org; searched on 18 April 2013.

Guruvaiah, M., D. Shah and E. Shah  2014.  Biomass and lipid accumulation of microalgae grown on dairy wastewater as a possible feedstock for biodiesel production.  International Journal of Science and Research 3(12):909-913.

Illman, A.M., A.H. Scragg and S.W. Shales  2000.  Increase in Chlorella strains calorific values when grown in low nitrogen medium.  Enzyme and Microbial Technology 27:631-635.

Krienitz, L., V.A.R. Huss and C. Bock  2014.  Chlorella:  125 years of the gre4en survivalist.  Trends in Plant Science xx:1-3 (in press).

Skorupskaite, V., V. Makareviciend and D. Levisauskas  2015.  Optimization of mixotrophic cultivation of microalgae Chlorella sp. for biofuel production using response surface methodology.  Algal Research 7:45-50.

Watanabe, A.  1960.  List of algal strains in the collection at the Institute of Applied Microbiology, University of Tokyo.  Journal of General Applied Microbiology 6:283-292.

Wang, X., E. Nordlander, E. Thorin and J. Yan  2013.  Microalgal biomethane production integrated with an existing biogas plant:  A case study in Sweden.  Applied Energy 112:468-484.