A microorganism resistant to high temperatures and producing alkaline proteases was isolated from soil samples from a protein-rich region (Kırıkkale/Yahşihan). This isolate, with high protein production, was identified as ORSK-4 by determining its morphological and biochemical properties using the 16s rRNA molecular approach and the Amplified ribosomal DNA restriction analysis (ARDRA) technique employed in strain differentiation. The optimum enzyme production conditions of the strain ORSK-4 were found to be the enzyme media, 3 days of incubation, 27.0 °C, and pH 7.0. Different components were utilized to determine the effect of changing the medium content on enzyme activity. Under the optimal production conditions determined in this way, the enzyme activity of ORSK-4 was found to be higher than that of some ATCC reference Bacillus species. To purify the extracellular protease of ORSK-4, precipitation with ammonium sulfate (30% and 80%), dialysis, and DEAE ion exchange chromatography were performed. SDS-PAGE analysis determined the molecular weight of the purified enzyme as approximately 30 kDa. Although the enzyme showed activity at various pH ranges, it showed its maximum activity when increased up to pH 9.0. In conclusion, the stability of the obtained alkaline protease enzyme under different conditions shows that it can be used in industrial and environmental applications.
Protease Bacillus molecular identification purification enzyme characterization
BAP 2016/067
BAP 2016/067
Birincil Dil | İngilizce |
---|---|
Konular | Enzimler, Endüstriyel Mikrobiyoloji , Endüstriyel Biyoteknoloji (Diğer) |
Bölüm | Araştırma Makaleleri |
Yazarlar | |
Proje Numarası | BAP 2016/067 |
Yayımlanma Tarihi | 30 Haziran 2024 |
Gönderilme Tarihi | 7 Şubat 2024 |
Kabul Tarihi | 22 Mart 2024 |
Yayımlandığı Sayı | Yıl 2024 Cilt: 7 Sayı: 1 |