Dykstra C C, Kushner S R
J Bacteriol. 1985 Sep;163(3):1055-9. doi: 10.1128/jb.163.3.1055-1059.1985.
Analysis of the cloned protease III gene (ptr) from Escherichia coli K-12 has demonstrated that in addition to the previously characterized 110,000-Mr protease III protein, a second 50,000-Mr polypeptide (p50) is derived from the amino-terminal end of the coding sequence. The p50 polypeptide is found predominantly in the periplasmic space along with protease III, but does not proteolytically degrade insulin, a substrate for protease III. p50 does not appear to originate from autolysis of the larger protein. Protease III is not essential for normal cell growth since deletion of the structural gene causes no observed alterations in the phenotypic properties of the bacteria. A 30-fold overproduction of protease III does not affect cell viability. A simple new purification method for protease III is described.
对来自大肠杆菌K-12的克隆蛋白酶III基因(ptr)的分析表明,除了先前鉴定的110,000道尔顿的蛋白酶III蛋白外,编码序列的氨基末端还衍生出第二种50,000道尔顿的多肽(p50)。p50多肽主要与蛋白酶III一起存在于周质空间中,但不会对蛋白酶III的底物胰岛素进行蛋白水解降解。p50似乎并非源自较大蛋白质的自溶。蛋白酶III对于正常细胞生长并非必需,因为结构基因的缺失未导致细菌表型特性出现可观察到的改变。蛋白酶III过量表达30倍并不影响细胞活力。本文描述了一种简单的蛋白酶III新纯化方法。