Isolation, Production, and Characterization of Protease from Bacillus subtilis IB No. 11
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A potent protein degrading bacterium was isolated from soil samples of different environments. Polyphasic taxonomic studies and phylogenetic 16S rRNA sequence analyses led to identify the isolate IB No. 11 as a strain of Bacillus subtilis. The isolated strain was recognized to produce protease constitutively, and the maximum production(1.64 units/ml) was attained in a shake flask culture when the isolate was grown at 40℃, for 32 h in basal medium supplemented with starch(0.25%) and gelatin(1.25%) as sole carbon and nitrogen source, respectively. The optimum pH and temperature for the protease activity were determined to be pH 7.0 and 50℃, respectively. Ca2+ and Mn2+ enhanced remarkably the protease activity but neither showed positive effect on the protease's thermal stability. In addition, it was observed that the protease was fairly stable in the pH range of 6.5-8.0 and at temperatures below 50℃, and it could be a good candidate for an animal feed additive. The inhibition profile of the protease by various inhibitors indicated that the enzyme is a member of serine-proteases. A combination of UV irradiation and NTG mutagenesis allowed to develop a protease hyper-producing mutant strain coded as IB No. 11-4. This mutant strain produced approximately 3.23-fold higher protease activity(6.74 units/mg) than the parent strain IB No. 11 when grown at 40℃ for 32h in the production medium. The protease production profile of the selected mutants was also confirmed by the zymography analysis.
Abstract
A potent protein degrading bacterium was isolated from soil samples of different environments. Polyphasic taxonomic studies and phylogenetic 16S rRNA sequence analyses led to identify the isolate IB No. 11 as a strain of Bacillus subtilis. The isolated strain was recognized to produce protease constitutively, and the maximum production(1.64 units/ml) was attained in a shake flask culture when the isolate was grown at 40℃, for 32 h in basal medium supplemented with starch(0.25%) and gelatin(1.25%) as sole carbon and nitrogen source, respectively. The optimum pH and temperature for the protease activity were determined to be pH 7.0 and 50℃, respectively. Ca2+ and Mn2+ enhanced remarkably the protease activity but neither showed positive effect on the protease's thermal stability. In addition, it was observed that the protease was fairly stable in the pH range of 6.5-8.0 and at temperatures below 50℃, and it could be a good candidate for an animal feed additive. The inhibition profile of the protease by various inhibitors indicated that the enzyme is a member of serine-proteases. A combination of UV irradiation and NTG mutagenesis allowed to develop a protease hyper-producing mutant strain coded as IB No. 11-4. This mutant strain produced approximately 3.23-fold higher protease activity(6.74 units/mg) than the parent strain IB No. 11 when grown at 40℃ for 32h in the production medium. The protease production profile of the selected mutants was also confirmed by the zymography analysis.
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