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International Journal of MicrobiologyVolume 2012 2012, Article ID 578925, 5 pages

Research Article

Department of Biotechnology, National Institute of Technology, Raipur 492 010, India

Indian Institute of Technology Delhi, New Delhi 110016, India

Received 29 July 2011; Accepted 11 October 2011

Academic Editor: Todd R. Callaway

Copyright © 2012 Pratima Gupta et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Eight isolates of cellulose-degrading bacteria CDB were isolated from four different invertebrates termite, snail, caterpillar, and bookworm by enriching the basal culture medium with filter paper as substrate for cellulose degradation. To indicate the cellulase activity of the organisms, diameter of clear zone around the colony and hydrolytic value on cellulose Congo Red agar media were measured. CDB 8 and CDB 10 exhibited the maximum zone of clearance around the colony with diameter of 45 and 50 mm and with the hydrolytic value of 9 and 9.8, respectively. The enzyme assays for two enzymes, filter paper cellulase FPC, and cellulase endoglucanase, were examined by methods recommended by the International Union of Pure and Applied Chemistry IUPAC. The extracellular cellulase activities ranged from 0.012 to 0.196 IU-mL for FPC and 0.162 to 0.400 IU-mL for endoglucanase assay. All the cultures were also further tested for their capacity to degrade filter paper by gravimetric method. The maximum filter paper degradation percentage was estimated to be 65.7 for CDB 8. Selected bacterial isolates CDB 2, 7, 8, and 10 were co-cultured with Saccharomyces cerevisiae for simultaneous saccharification and fermentation. Ethanol production was positively tested after five days of incubation with acidified potassium dichromate.

Autor: Pratima Gupta, Kalpana Samant, and Avinash Sahu



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