Studies on Alkaline Serine Protease Produced by Bacillus clausii GMBE 22

Abstract

An alkali tolerant Bacillus strain having extracellular serine alkaline protease activity was newly isolated from compost and identified as Bacillus clausii GMBE 22. An alkaline protease (AP22) was 4.66-fold purified in 51.5% yield from Bacillus clausii GMBE 22 by ethanol precipitation and DEAE-cellulose anion exchange chromatography. The purified enzyme was identified as serine protease by LC-ESI-MS analysis. Its complete inhibition by phenylmethanesulfonylfluoride (PMSF) also justified that it is a serine alkaline protease. The molecular weight of the enzyme is 25.4 kDa. Optimal temperature and pH values are 60°C and 12.0, respectively. The enzyme showed highest specificity to N-Suc-Ala-Ala-Pro-Phe-pNA. The K_m and k_cat values for hydrolysis of this substrate are 0.347 mM and 1141 min⁻¹ respectively. The enzyme was affected by surface active agents to varying extents. The enzyme is stable for 2 h at 30°C and pH 10.5. AP22 is also stable for 5 days over the pH range 9.0–11.0 at room temperature. AP22 has good pH stability compared with the alkaline proteases belonging to other strains of Bacillus clausii reported in the literature.

Keywords:

• Alkaline protease
• Bacillus clausii
• Enzyme purification and characterisation
• Serine protease

ACKNOWLEDGMENT

This research was supported by Marmara University (BAPKO) by the project number BSE – 073/1311.

Notes

∗Results of Denizci et al.,^{[ 5 ]} ND; No data available.

∗Results from Denizci et al.^{[ 5 ]}

∗Results from Denizci et al.^{[ 5 ]}