To optimize the fermentation medium for production of alkaline protease by Bacillus licheniformis MZK05M9 (BlM9) molasses as carbon source, soybean meal as nitrogen source and the salts NaCl, MgSO4.7H2O and K2HPO4 were selected by Plackett-Burman approach. The Response Surface Methodology (RSM) based on Central Composite Design (CCD) revealed that the optimum values for the tested variables were found as (% w/v) molasses 0.92, soybean meal 0.79, NaCl 0.125, MgSO4 0.125 and K2HPO4 0.59 with the protease activity 761 U/ml predicted by statistical software Minitab Version 17. The experimental value was found as 765 U/ml. The granular size of soybean meal 4.7 mm supported the enzyme production 5 % higher than that of the mixed sizes between 6 to 4 mm. Fermentation in 7 l bioreactor exhibited the enzyme activity 1020 U/ml after 28 h. The statistically optimized medium based on cost-effective agro-industrial C and N sources yielded a high productivity 36428 U/l h of protease by the mutant strain of B. licheniformis.
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Year
Month
Isolation and optimization of alkaline protease producing Bacteria from undisturbed soil of NE-region of India falling under Indo-Burma biodiversity hotspots
Onkar Nath Tiwari, Thiyam Bidyababy Devi, Kangjam Sarabati Devi, Gunapati Oinam, Thingujam Indrama, Keithellakpam Ojit, Oinam Avijeet, Lakreiphy NingshenPurification and characterization of extracellular alkaline protease from Streptomyces sp. LCJ12A isolated from Pichavaram mangroves
M. Parthasarathy, J. Joel GnanadossMedia optimization for the production of alkaline protease by Bacillus cereus PW3A using response surface methodology
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