Jensen S E, Fecycz I T, Stemke G W, Campbell J N
Can J Microbiol. 1980 Jan;26(1):87-93. doi: 10.1139/m80-013.
The enzymatically active form of protease 1, the major exocellular protein produced by Pseudomonas aeruginosa strain 34362, has been shown to exist exclusively exocellularly with no significant cell-associated activity. However, the presence of a cell-associated, enzymatically inactive protein which is serologically cross-reactive with, and convertible to, active enzyme has been demonstrated. One method of conversion of "precursor" to active enzyme is via limited proteolysis. Two assay systems for precursor were developed, one a radioimmune assay, and the other a proteolytic activation procedure. Localization studies suggest that the association while more tenacious than classical periplasmic enzymes is still an ionic rather than a covalent one. Kinetics of production studies showed to precursor to be synthesized early in the growth cycle and to accumulate prior to the rapid release of the active enzyme. Molecular weight studies showed only slight changes produced upon activation.
蛋白酶1是铜绿假单胞菌34362菌株产生的主要胞外蛋白,其酶活性形式仅存在于胞外,细胞相关活性不显著。然而,已证明存在一种与活性酶具有血清学交叉反应且可转化为活性酶的细胞相关的无酶活性蛋白。将“前体”转化为活性酶的一种方法是通过有限的蛋白水解。开发了两种前体检测系统,一种是放射免疫测定法,另一种是蛋白水解激活程序。定位研究表明,这种结合虽然比经典的周质酶更紧密,但仍然是离子性的而非共价性的。生产动力学研究表明,前体在生长周期早期合成,并在活性酶快速释放之前积累。分子量研究表明激活后仅产生轻微变化。