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http://dx.doi.org/10.4014/jmb.1203.03021

Scale-Up of an Alkaline Protease from Bacillus pumilus MTCC 7514 Utilizing Fish Meal as a Sole Source of Nutrients  

Gupta, Rishikesh Kumar (Department of Biotechnology, Central Leather Research Institute)
Prasad, Dinesh (Department of Biotechnology, Central Leather Research Institute)
Sathesh, Jaykumar (Department of Biotechnology, Central Leather Research Institute)
Naidu, Ramachandra Boopathy (Department of Biotechnology, Central Leather Research Institute)
Kamini, Numbi Ramudu (Department of Biotechnology, Central Leather Research Institute)
Palanivel, Saravanan (Department of Biotechnology, Central Leather Research Institute)
Gowthaman, Marichetti Kuppuswami (Department of Biotechnology, Central Leather Research Institute)
Publication Information
Journal of Microbiology and Biotechnology / v.22, no.9, 2012 , pp. 1230-1236 More about this Journal
Abstract
Fish meal grades SL1 and SL2 from Sardine (Sardinella longiceps) and NJ from Pink Perch (Nemipterus japonicas) were evaluated as a sole source of carbon and nitrogen in the medium for alkaline protease production by Bacillus pumilus MTCC 7514. The analysis of the fish meal suggests that the carbon and nitrogen contents in fish meal are sufficient to justify its choice as replacement for other nutrients. Protease production increased significantly (4,914 U/ml) in medium containing only fish meal, compared with the basal medium (2,646 U/ml). However, the elimination of inorganic salts from media reduced the protease productivity. In addition, all the three grades of fish meal yielded almost the same amounts of protease when employed as the sole source of carbon and nitrogen. Nevertheless, the best results were observed in fish meal SL1 medium. Furthermore, protease production was enhanced to 6,966 U/ml and 7,047 U/ml on scaling up from flask (4,914 U/ml) to 3.7 and 20 L fermenters, respectively, using fish meal (10 g/l). Similarly, the corresponding improvement in productivities over flask (102.38 U/ml/h) was 193.5 and 195.75 U/ml/h in 3.7 and 20 L fermenters, respectively. The crude protease was found to have dehairing ability in leather processing, which is bound to have great environmental benefits.
Keywords
Fish meal; protease; dehairing; scale-up; fermenters;
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1 Blanco, M., C. G. Sotelo, M. J. Chapela, and R. I. Perez-Martin. 2007. Towards sustainable and efficient use of fishery resources: Present and future trends. Trends Food Sci. Technol. 18: 29-36.   DOI   ScienceOn
2 Ellouz, Y., A. Bayuodh, S. Kammoun, N. Gharsallah, and M. Narsi. 2001. Production of protease by Bacillus subtilis grown on sardinelle heads and viscera flour. Bioresour. Technol. 80: 49-51.   DOI   ScienceOn
3 Ellouz, Y. T., B. Ghorbel, N. Souissi, S. Kammoun, and M. Nasri. 2003. Biosynthesis of protease by Pseudomonas aeruginosa MN7 grown on fish substrate. World J. Microbiol. Biotechnol. 19: 41-45.   DOI   ScienceOn
4 Hadj-Ali, N. E., N. Hmidet, N. Souissi, A. S. Kamoun, and M. Nasri. 2010. The use of an economical medium for the production of alkaline serine proteases by Bacillus licheniformis NH1. Afr. J. Biotechnol. 9: 2668-2674.
5 Huang, Q., Y. Peng, X. Li, H. Wang, and Y. Zhang. 2003. Purification and characterization of an extracellular alkaline serine protease with dehairing function from Bacillus pumilus. Curr. Microbiol. 46: 169-173.   DOI   ScienceOn
6 Joo, H. S. and C. S. Chang. 2005. Production of protease from a new alkalophilic Bacillus sp. I-312 grown on soybean meal: Optimization and some properties. Process Biochem. 40: 1263-1270.   DOI   ScienceOn
7 Kamoun, A. S., B. Ghorbel-Frikha, A. Haddar, and M. Nasri. 2010. Enhanced Bacillus cereus BG1 protease production by the use of sardinelle (Sardinella aurita) powder. Ann. Microbiol. 61: 273-280.
8 Kumar, A. G., N. Nagesh, T. G. Prabhakar, and G. Sekaran. 2008. Purification of extracellular acid protease and analysis of fermentation metabolites by Synergistes sp. utilizing proteinaceous solid waste from tanneries. Bioresour. Technol. 99: 2364-2372.   DOI   ScienceOn
9 Kunitz, M. 1947. Crystalline soyabean trypsin inhibitor II. General properties. J. Gen. Physiol. 30: 291-310.   DOI
10 Nadeem, M., J. I. Qazi, and S. Baig. 2009. Effect of aeration and agitation rates on alkaline protease production by Bacillus licheniformis UV-9 mutant. Turk. J. Biochem. 34: 89-96.
11 Prabhawathi, V. 2010. Protease from Bacillus pumilus - Isolation, production, purification, characterization and its potential [dissertation]. University of Madras, Chennai (TN), India.
12 Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular Cloning: A Laboratory Manual, 2nd Ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
13 Venugopal, V. 1994. Production of fish protein hydrolysates by microorganisms, pp. 223-239. In A. M. Martin (ed.). Fisheries Processing: Biotechnological Applications. Chapman and Hall, London.
14 Seeta Laxman, R., A. P. Sonawane, S. V. More, B. S. Rao, M. V. Rele, V. V. Jogdand, et al. 2005. Optimization and scale up of production of alkaline protease from Conidiobolus coronatus. Process Biochem. 40: 3152-3158.   DOI   ScienceOn
15 Singh, J., R. M. Vohra, and D. K. Sahoo. 2004. Enhanced production of alkaline proteases by Bacillus sphaericus using fed-batch culture. Process Biochem. 39: 1093-1101.   DOI   ScienceOn
16 Souissi, N., Y. T. Ellouz, A. Bougatef, M. Blibech, and M. Nasri. 2008. Preparation and use of media for protease-producing bacterial strains based on by-products from cuttlefish (Sepia officinalis) and wastewaters from marine-products processing factories. Microbiol. Res. 163: 473-480.   DOI   ScienceOn
17 Wang, R., R. C. S Law, and C. Webb. 2005. Protease production and conidiation by Aspergillus oryzae in flour fermentation. Process Biochem. 40: 217-227.   DOI   ScienceOn