Application of Acinetobacter sp. KKU44 for Cellulase Production from Agricultural Waste
Authors: Surasak Siripornadulsil, Nutt Poomai, Wilailak Siripornadulsil
Abstract:
Due to a high ethanol demand, the approach for effective ethanol production is important and has been developed rapidly worldwide. Several agricultural wastes are highly abundant in celluloses and the effective cellulase enzymes do exist widely among microorganisms. Accordingly, the cellulose degradation using microbial cellulase to produce a low-cost substrate for ethanol production has attracted more attention. In this study, the cellulase producing bacterial strain has been isolated from rich straw and identified by 16S rDNA sequence analysis as Acinetobacter sp. KKU44. This strain is able to grow and exhibit the cellulase activity. The optimal temperature for its growth and cellulase production is 37°C. The optimal temperature of bacterial cellulase activity is 60°C. The cellulase enzyme from Acinetobacter sp. KKU44 is heat-tolerant enzyme. The bacterial culture of 36h. showed highest cellulase activity at 120U/mL when grown in LB medium containing 2% (w/v). The capability of Acinetobacter sp. KKU44 to grow in cellulosic agricultural wastes as a sole carbon source and exhibiting the high cellulase activity at high temperature suggested that this strain could be potentially developed further as a cellulose degrading strain for a production of low-cost substrate used in ethanol production.
Keywords: Acinetobacter sp. KKU44, bagasse, cellulase enzyme, rice husk.
Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1092086
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Razmovski, R., Vucurovic, V. (2012) Bioethanol production from sugar beet molasses and thick juice using Saccharomyces cerevisiae immobilized on maize stem ground tissue. Fuel 92(1): 1–8.[2] Lee, Y.J., Kim, B.K., Lee, B.H., Jo, K.I., Lee, N.K., Chung, C.H., Lee, Y.C., Lee, J.W. (2008) Purification and characterization of cellulase produced by Bacillus amyoliquefaciens DL-3 utilizing rice hull. Bioresource Technol 99(2): 378–386.
[3] Sarkar, N . , Ghosh, S.K., Bannerjee, S., Aikat, K. (2012) Bioethanol production from agricultural wastes: An overview. Renew Energ 37(1): 19–27.
[4] Lo, Y . C . , Li, W.C., Chen, C.Y., Chen, W.M., Chang, J.S. (2010) Characterization and high-level production of xylanase from an indigenous cellulolytic bacterium Acinetobacter junii F6-02 from southern Taiwan soil. Biochem Eng J 53(1): 77–84.
[5] Acharya, S., Chaudhary, A. (2012) Optimization of fermentation conditions for cellulases production by Bacillus licheniformis MVS1 and Bacillus sp. MVS3 isolated from Indian hot Spring. Braz Arch Biol Tech 55(4): 497-503.
[6] Miller, G . L . , Blum, R., Glennon, W.E., Burton A.L. (1960) Measurement of carboxymethyl cellulase activity. Anal Biochem 2: 127–132.
[7] Mawadza, C . , Hatti-Kaul, R., Zvauya, R., Mattiasson, B. (2000) Purification and characterization of cellulases produced by two Bacillus strains. J Biotechnol 83(3): 177–187.
[8] Singh, R., Kumar, R., Bishnoi, K., Bishnoi, N.R. (2009) Optimization of synergistic parameters for thermostable cellulase activity of Aspergillus heteromorphus using response surface methodology. Biochem Eng J 48(1): 28–35.