Cellulase Producing Bacteria from the Wood-Yards on Kallai River Bank

Abstract

This study evaluates the influence of growth parameters such as pH, temperature, Carboxy Methyl Cellulose (CMC) concentration and agitation on cellulase production from three bacterial strains, viz., Achromobacter xylosoxidans BSS4, Bacillus sp. BSS3 and Pseudomonas sp. BSS2 isolated from the wood-yards on Kallai river bank in Kerala. Production of cellulase by these isolates was detected using basal salt medium (BSM) with 0.5% CMC as supplement, and CMCase activity was confirmed by iodine test. Dinitrosalicylic acid method was employed for assaying the cellulase production by measuring the amount of glucose liberated in μmol/mL/min. Maximum enzyme production from Pseudomonas sp. BSS2 was at pH 8, 37 with 1% CMC and 150 rpm, and cellulase production increased from initial 49.84 U/mL to 91.28 U/mL after optimization. The highest enzyme activity from Bacillus sp. BSS3 was at pH 9, 37 with 1% CMC, 150 rpm, and cellulase production increased from initial 26.05 U/mL to 104.68 U/mL after optimization. The maximum enzyme production from A. xylosoxidans BSS4 was at pH 7, 40 with 0.5% CMC and 150 rpm, and cellulase production increased from initial 55.28 U/mL to 68.37 U/mL after optimization. Thus among the three isolates, Bacillus sp. BSS3 showed maximum enzyme yield which can be explored for further scale up studies with an industrial perspective.

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S. Sreedevi, S. Sajith and S. Benjamin, "Cellulase Producing Bacteria from the Wood-Yards on Kallai River Bank," Advances in Microbiology, Vol. 3 No. 4, 2013, pp. 326-332. doi: 10.4236/aim.2013.34046.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] G. Coral, B. Arikan, M. N. Unaldi and H. Gunvenmes, “Some Properties of Crude Carboxymethyl Cellulase of Aspergillus niger Z10 Wild Type Strain,” Turkish Journal of Biology, Vol. 26, No. 4, 2002, pp. 209-221.
[2] Y. H. P. Zhang, D. J. Schell and J. D. Mc Millan, “Methodological Analysis for Determination of Enzymatic Digestibility of Cellulosic Materials,” Biotechnology and Bioengineering, Vol. 96, No. 1, 2007, pp. 188-194. doi:10.1002/bit.21178
[3] R. K. Sukumaran, R. R. Singhania and A. Pandey, “Microbial Cellulases—Production Applications and Challenges,” Journal of Scientific and Industrial Research, Vol. 64, No. 11, 2005, pp. 832-844.
[4] A. E. Humphrey, “The Hydrolysis of Cellulosic Materials to Useful Products,” In: R. D. Brown, Jr. and L. Jurasek, Eds., Hydrolysis of Cellulose: Mechanisms of Enzymatic and Acid Catalysis, University of Pennyslvania, Philadelphia, 1979, pp. 25-53.
[5] T. P. Noyola and M. D. Torre, “Regulation of Cellulases and Xylanases from a Derepressed Mutant of Cellulomonas flavigena Growing on Sugarcane Bagasse in Continous Culture,” Bioresouce Technology, Vol. 78, No. 3, 2001, pp. 285-291. doi:10.1016/S0960-8524(00)00181-4
[6] M. Maki, K. T. Lenng and Q. Wensheng, “The Prospects of Cellulase Producing Bacteria for the Bioconversion of Lignocellulosic Biomass,” Journal of Biological Science, Vol. 5, No. 5, 2009, pp. 500-516.
[7] J. S. Tolan and B. Foody, “Cellulase from Submerged Fermentation,” In: G. T. Tsao, Ed., Recent Progress in Bioconversion of Lignocellulosics, 65th Edition, Springer Publishing, Berlin, 1999, pp. 41-67.
[8] L. Hankin and S. Anagnostakis, “Solid Media Containing CMC to Detect CM Cellulase Activity of Microorganisms,” Journal of General Microbiology, Vol. 98, No. 1, 1977, pp. 109-115. doi:10.1099/00221287-98-1-109
[9] R. C. Kasana, R. Salwan, H. Dhar, S. Dutt and A. Gulati, “A Rapid and Easy Method for the Detection of Microbial Cellulases on Agar Plates Using Gram’s Iodine,” Current Microbiology, Vol. 57, No. 5, 2008, pp. 503-507. doi:10.1007/s00284-008-9276-8
[10] G. L. Miller, “Use of Dinitrosalicyclic Acid Reagent for Determination of Reducing Sugar,” Analytical Chemistry, Vol. 31, No. 3, pp. 426-428. doi:10.1021/ac60147a030
[11] K. L. Kalra, G. Kocher and G. Banta, “Optimization of Cellulase Production by Submerged Fermentation of Rice Straw by Trichoderma harzianum RUT-C 8280,” The Internet Journal of Microbiology, Vol. 5, No. 2, 2008, pp. 1-7.
[12] K. Hirasawa, K. Uchimura, M. Kashima, W. D. Grant, S. Ito, T. Kobayashi and K. Horikoshi, “Salt Activated Endoglucanase of a Strain of Alkaliphilic Bacillus agaradhaerens,” Antonie Van Leuvenhoek, Vol. 89, No. 2, 2006, pp. 211-219. doi:10.1007/s10482-005-9023-0
[13] R. H. Doi, “Cellulases of Mesophilic Microorganisms: Cellulosome and Non Cellulosome Producers,” Annals of New York Academy of Sciences, Vol. 1125, No. 1, 2008, pp. 267-279. doi:10.1196/annals.1419.002
[14] M. Rubeena, K. Neethu, S. Sajith, S. Sreedevi, P. Prakasan, K. N. Unni, M. K. Sarath Josh, V. N. Jisha, S. Pradeep and S. Benjamin, “Lignocellulolytic Activities of a Novel Strain of Trichoderma harzianum,” Advances in Bioscience and Biotechnology, Vol. 4, No. 2, 2013, pp. 214-221. doi:10.4236/abb.2013.42030
[15] S. Y. Kim, S. W. Kang and J. S. Lee, “Cellulase and Xylanase Production by Aspergillus niger KKS in Various Bioreactors,” Bioresource Technology, Vol. 59, No. 1, 1997, pp. 63-67. doi:10.1016/S0960-8524(96)00127-7
[16] K. Neethu, M. Rubeena, S. Sajith, S. Sreedevi, P. Priji, K. N. Unni, M. K. Sarath Josh, V. N. Jisha, S. Pradeep and S. Benjamin, “A Novel Strain of Trichoderma viride Shows Complete Lignocellulolytic Activities,” Advances in Bioscience and Biotechnology, Vol. 3, No. 8, pp. 1160-1166.
[17] V. W. Yang, Z. Zhang, G. Elegir and T. W. Jeffries, “Alkaline Active Xylanase Produced by an Alkaliphilic Bacillus Species Isolated from Kraft Pulp,” Journal of Industrial microbiology, Vol. 15, No. 5, 1995, pp. 434-441. doi:10.1007/BF01569971
[18] S. Acharya and A. Chaudary, “Effect of Nutritional and Environmental Factors on Cellulases Activity by Thermophilic Bacteria Isolated from Hot Spring,” Journal of Scientific and Industrial Research, Vol. 70, No. 2, 2011, pp. 142-148.
[19] G. Immanuel, R. Dhanusa, P. Prema and A. Palavesam, “Effect of Different Growth Parameters on Endoglucanase Enzyme Activity by Bacteria Isolated from Coir Retting Effluents of Estuarine Environment,” International Journal of Environment Science and Technology, Vol. 3, No. 1, 2006, pp. 25-34.
[20] O. E. Fagade and O. O. Bamigboye, “Effect of Cultural Conditions on the Cellulase Activity of Bacteria Species Isolated from Degrading Corn Cob,” Archives of Applied Science Research, Vol. 4, No. 6, 2012, pp. 2540-2545.
[21] L. Lin, X. Kan, H. Yan and D. Wang, “Characterization of Extracellular Cellulose-Degrading Enzymes from Bacillus thuringiensis Strains,” Electronic Journal of Biotechnology, Vol. 15, No. 3, 2012, pp. 1-7. doi:10.2225/vol15-issue3-fulltext-1
[22] A. Taleb, A. A. Khadiga, W. A. Mashhoor, A. N. Sohair, M. S. Sharaf and H. M. Hoda, “Nutritional and Environmental Factors Affecting Cellulase Production by Two Strains of Cellulolytic Bacilli”, Australian Journal of Basic and Applied Sciences, Vol. 3, No. 3, 2009, pp. 2429-2436.
[23] A. Ray, A. Bairagi, K. S. Ghosh and S. K. Sen, “Optimization of Fermentation Conditions for Cellulase Production by Bacillus subtilis CY5 and Bacillus Circulans TP3 Isolated From Fish Gut,” Acta Ichthyologica Et Piscatoria, Vol. 37, No. 1, 2007, pp. 47-53.
[24] T. Shankar and L. Isaiarasu, “Cellulase Production by Bacillus pumilus EWBCM1 under Varying Cultural Conditions,” Middle East Journal of Scientific Research, Vol. 8, No. 1, 2011, pp. 40-45.
[25] G. S. Kumar, M. S. Chandra, M. Sumanth, A. Vishnupriya, B. R. Reddy and Y. L. Choi, “Cellulolytic Enzymes Production from Submerged Fermentation of Different Substrates by Newly Isolated Bacillus spp. FME,” Journal of Korean Society Applied Biological Chemistry, Vol. 52, No. 1, 2009, pp. 17-21. doi:10.3839/jksabc.2009.003
[26] F. D. Otajevwo and H. S. A. Aluyi, “Cultural Conditons Necessary for Optimal Cellulase Yield by Cellulolytic Bacterial Organisms as They Relate to Residual Sugars Released in Broth Medium,” Modern Applied Science, Vol. 5, No. 3, 2011, pp. 141-151.

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