Department of Biochemistry, Vels University Chennai India, 600 117.
Braz J Microbiol. 2010 Jan;41(1):179-85. doi: 10.1590/S1517-838220100001000026. Epub 2010 Mar 1.
This study was aimed at producing protease and lipase simultaneously on a common medium by Bacillus licheniformis VSG1, which was isolated from a tannery effluent. The effect of media composition with respect to protein source, lipid source and emulsifier on the production of protease and lipase was analysed. Both those enzymes were produced under optimized conditions like pH, temperature and incubation time. The enzyme mixture comprising of both protease and lipase was purified by ammonium sulphate precipitation, dialysis and gel filtration chromatography to obtain 20-fold pure enzymes. The purified enzyme mixture was characterized to determine the optimum pH and temperature of protease and lipase, the response of the enzymes to inhibitors, additives and solvents. The molecular weight of both the enzymes was determined as 40 kDa on SDS-PAGE. The concomitant production of protease and lipase and the purification of both the enzymes in a single mixture have industrial significance, as many industrial processes use both protease and lipase together.
本研究旨在通过从制革厂废水中分离出的地衣芽孢杆菌 VSG1 在同一培养基中同时生产蛋白酶和脂肪酶。分析了培养基组成对蛋白酶和脂肪酶产生的影响,包括蛋白质源、脂肪源和乳化剂。在优化条件下,如 pH 值、温度和孵育时间,两种酶都得到了生产。用硫酸铵沉淀、透析和凝胶过滤层析对包含蛋白酶和脂肪酶的酶混合物进行纯化,得到 20 倍纯的酶。对纯化的酶混合物进行了特性分析,以确定蛋白酶和脂肪酶的最适 pH 值和温度、酶对抑制剂、添加剂和溶剂的反应。两种酶的分子量均在 SDS-PAGE 上确定为 40 kDa。同时生产蛋白酶和脂肪酶,并在单一混合物中纯化两种酶,具有工业意义,因为许多工业过程都同时使用蛋白酶和脂肪酶。