炭疽杆菌
炭疽毒素
大肠杆菌
周质间隙
胞浆
微生物学
生物化学
生物活性
细胞质
生物
钙调蛋白
细菌
化学
重组DNA
酶
体外
融合蛋白
基因
遗传学
作者
Bridget A. Cooksey,Gavin C. Sampey,J.L. Pierre,Xian‐En Zhang,Jeffrey D. Karwoski,Gil H. Choi,Michael W. Laird
摘要
Anthrax is caused by the gram-positive spore-forming bacterium Bacillus anthracis. The anthrax toxin consists of three proteins, protective antigen (PA), lethal factor (LF), and edema factor (EF). PA facilitates the translocation of LF and EF into the cytosol of mammalian cells. LF is thought to be a zinc-dependent metalloprotease that results in death. EF is a calmodulin- and calcium-dependent adenylate cyclase that causes edema upon entrance into the cytosol by elevating the cAMP levels in cells. Previous efforts to produce recombinant EF (rEF) in Escherichia coli yielded only 2.5 mg of rEF per liter of culture. In this work, we produced soluble rEF in large quantities in both the periplasm and cytoplasm of E. coli from shake flasks and fermentors. The rEF protein was purified by standard chromatography and yielded >97% pure, biologically active rEF. Yields of purified rEF from medium cell density fermentations resulted in up to 2.38 g/L of highly pure, biologically active rEF protein. These results exhibit the ability to generate gram quantities of active rEF from E. coli.
科研通智能强力驱动
Strongly Powered by AbleSci AI