Innovation Center, Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11001 Belgrade, Serbia.
Bioresour Technol. 2011 Dec;102(24):11226-33. doi: 10.1016/j.biortech.2011.09.076. Epub 2011 Sep 29.
An indigenous Pseudomonas aeruginosa strain has been studied for lipase and protease activities for their potential application in detergents. Produced enzymes were investigated in order to assess their compatibility with several surfactants, oxidizing agents and commercial detergents. The crude lipase appeared to retain high activity and stability in the presence of several surfactants and oxidizing agents and it was insusceptible to proteolysis. Lutensol® XP80 and Triton® X-100 strongly activated the lipase for a long period (up to 40 and 30% against the control after 1h) while the protease activity was enhanced by the addition of Triton® WR1339 and Tween® 80. The washing performance of the investigated surfactants was significantly improved with the addition of the crude enzyme preparation. Studies were further undertaken to improve enzymes production. The optimization of fermentation conditions led to an 8-fold increase of lipase production, while the production of protease was enhanced by 60%.
已针对脂酶和蛋白酶活性对一株土著铜绿假单胞菌进行了研究,以期将其应用于洗涤剂中。为了评估这些酶与几种表面活性剂、氧化剂和商业洗涤剂的兼容性,对其进行了研究。粗脂酶在存在几种表面活性剂和氧化剂的情况下似乎保持了高活性和稳定性,并且不易受到蛋白水解的影响。Lutensol® XP80 和 Triton® X-100 强烈激活脂酶的时间较长(1 小时后对照的 40%和 30%),而 Triton® WR1339 和 Tween® 80 的添加则增强了蛋白酶的活性。添加粗酶制剂可显著提高所研究的表面活性剂的洗涤性能。进一步进行了研究以提高酶的产量。发酵条件的优化使脂酶的产量增加了 8 倍,而蛋白酶的产量增加了 60%。