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Purification and Characterization of Neutral Protease from Bacillus substilis UBT7 Isolated from Terasi, Indonesian Fermented Fish

机译:从Terasi,印度尼西亚发酵鱼中分离的芽孢杆菌替代UBT7中性蛋白酶的纯化和表征

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Neutral protease producing bacterium Bacillus substilis UBT7 strain isolated from Terasi, an Indonesian fermented fish grew in shake flask and fermenter, and produced protease at 37 °C, pH 7 for 24 hour. After three purification steps, the enzyme was successfully purified. This neutral protease had an apparent molecular mass of 32 kDa as estimated by sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis. The enzyme was active optimum on 50 °C. This indicated that the enzyme was slightly thermozyme. The stability was decreased on 40 °C. The enzyme was optimum in pH 7. The enzyme was somehow enhanced with Fe~(2+) and K~(2+) metal ionsbut not by the addition of Ni~(2+).
机译:生产细菌的中性蛋白酶枯草芽孢杆菌含量的UBT7菌株从Terasi中分离,印度尼西亚发酵鱼在摇瓶和发酵罐中生长,并在37℃下产生蛋白酶,pH 7持续24小时。 三次纯化步骤后,成功纯化酶。 这种中性蛋白酶具有32kDa的表观分子量,如十二烷基硫酸钠(SDS)聚丙烯酰胺凝胶电泳估计。 酶在50℃下最佳最佳。 这表明酶略微热沸点。 稳定性在40℃下降低。 酶在pH7中最佳。酶以某种方式与Fe〜(2+)和K〜(2+)金属离子不通过添加Ni〜(2+)而增强。

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