SCREENING AND GROWTH KINETIC STUDIES OF WILD CHLOROPHYCEAN FRESH WATER MICROALGAL SPECIES FOR BIOMASS AND BIOFUEL APPLICATIONS

Authors

  • Sunil Kumar Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, Jharkhand 835215 India
  • Avneesh Pareek Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, Jharkhand 835215 India
  • Kunal Mukhopadhyay Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, Jharkhand 835215 India

Keywords:

Biofuel, Chlorophyceae, Lipid, Microalgae, Productivity

Abstract

Objective: Microalgae are studied for decades for various products such as, protein rich animal/fish feed, lipids, pigments, neutra ceuticals, therapeutic agents, primary products and biomass. Lipid content was prime target in most of the research programs for production of biodiesel as an alternate to fossil fuel. Chlorophycean microalgae has the potential to meet all these requirements. The objective of this study was to collect and identify chlorophycean microalgae from various water bodies of Jharkhand State of India and to estimate their total lipid content.

Methods: Wild cholorophycean fresh water species from Jharkhand were collected and studied for biomass, total lipid, carotenoids and chlorophyll content. Fourier transform infrared spectroscopy (FTIR) data were obtained for further verification of lipid estimation in all the species. Light microscopy as well as Scanning Electron Microscopy (SEM) was performed to identify the species.

Results: The observation revealed two groups of micro algae, among these Scenedesmus sp and Chlorella sp. Showed highest lipid accumulation of 45.1 and 41.5 % respectively, while Legerhemia sp. Showed highest biomass production (21.2 g/l). Productivity/day for an 80K L pond system was calculated by extrapolation of results; that changed the choice of organism to Desmodesmus sp.

Conclusion: The microalgae collected from highly polluted sites were efficient enough to yield high lipid (AKS-1/AKS-8) and biomass (AKS-6). The laboratory scale study was extrapolated with mass scale culture data and the choice of organism changed to AKS-16 from AKS-1/AKS-8 (for high lipid content) or AKS-6 (for high biomass).

 

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Author Biographies

Sunil Kumar, Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, Jharkhand 835215 India

Senior Research Scholar

Avneesh Pareek, Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, Jharkhand 835215 India

Assistant Professor

Kunal Mukhopadhyay, Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, Jharkhand 835215 India

Professor and Head

References

Chu W-L. Biotechnological applications of microalgae. Int E-J Sci Med Educ 2012;6:S24-S37.

Priyadarshani I, Rath B. Commercial and industrial applications of micro algae–A review. J Algal Biomass Util 2012;3(4):89-100.

http://web.biosci.utexas.edu/utex/mediaDetail.aspx?mediaID=147(page last visited: 17/10/2014)

Prescott GW. How to know: the freash water algae. WM. G BROWN company, Dubuque, IOWA http://cccryo.ntr.io/sources/files/medien/BBM.pdf(page last visited:17/02/2012).

Dayananda C, Sarada R, Kumar V, Ravishankar GA. Isolation and characterization of hydrocarbon producing green alga Botryococcus brauniifrom Indian freshwater bodies. Electron J Biotechnol 2007;10:78-91.

Moris GM, Costa JAV. Isolation and selection of microalgae from coal fired thermoelectric power plant for biofixation of carbon dioxide. Energy Convers Manage 2007;48(2):2169-73.

Gomez PI, Gonzalez MA. Genetic polymorphism in eight Chilean strains of the carotenogenic microalga Dunaliella salina. Biol Res 2001;34(1):23-30.

ChoiJ-S, ChoJ-Y, JinL-G, JinH-J, HongY-K. Procedures for the axenic isolation of conchocelis and monospores from the red seaweed Porphyra yezoensis. J Appl Phycol 2002;14:115–21.

Callowa JA, Osborne MP, Callowa ME, Baker F, Donald AM. Use of environmental scanning electron microscopy to image the spore adhesive of the marine alga Enteromorpha in its natural hydrated state. Colloides Surf 2003;27:315-21.

Bligh EG, Dyer WJ. A rapid method for total lipid extraction and purification. Can J Biochem Physiol 1959;37:911-7.

Litchtenthaller HK, Wellburn AR. Determination of total carotenoids and chlorophylls a and b of leaf in different solvents. Biol Soc Trans 1985;11:591-2.

Phukan MM, Chutia RS, Konwar BK, Katki R. Microalgae Chlorella as a potential bioenergy feedstock. Appl Energy 2011;88:3307-12.

Mahapatra DM, Ramachandra TV. Algal biofuel: bountiful lipid from Chlorococcumsp. proliferating in municipal wastewater. Curr Sci 2013;105(1):47-55.

Chisti Y. Biodiesel from microalgae. Biotechnol Adv 2007;25:294–306.

Ren H-Y, Liu B-F, Lei CM, Zhao, Ren N-Q. A new lipid-rich microalgaScenedesmus sp. strain R-16 isolated using Nile red staining: effects of carbon and nitrogen sources and initial pH on the biomass and lipid production. Biotechnol Biofuels 2013;6:143-52.

Stuart B. Infrared spectroscopy: fundamentals and applications. 1st ed. West Sussex: John Wiley and Sons, Ltd; 2004.

Dumas P, Miller L. The use of synchrotron infrared microspectroscopy in biological and biomedical investigations. Vib Spetrosc 2003;32:3–21.

Backmann J, Schultz C, Fabian H, Hahn U, Saenger W, Naumann D. Thermally induced hydrogen exchange processes in small proteins as seen by FTIR spectroscopy. Proteins Struct Funct Bioinf 1996;24:379–87.

Fischer G, Braun S, Thissen R, Dott W. FT-IR spectroscopy as a tool for rapid identification and intra-species characterization of airborne filamentous fungi. J Microbiol Meth 2006;64:63–77.

Published

01-01-2015

How to Cite

Kumar, S., A. Pareek, and K. Mukhopadhyay. “SCREENING AND GROWTH KINETIC STUDIES OF WILD CHLOROPHYCEAN FRESH WATER MICROALGAL SPECIES FOR BIOMASS AND BIOFUEL APPLICATIONS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 1, Jan. 2015, pp. 312-21, https://journals.innovareacademics.in/index.php/ijpps/article/view/3743.

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