Braunagel S C, Benedik M J
Department of Biology, Texas A & M University, College Station 77843-3258.
Mol Gen Genet. 1990 Jul;222(2-3):446-51. doi: 10.1007/BF00633854.
Utilizing the DNA sequence of the metalloprotease from Serratia strain E-15, we isolated and sequenced the homologous gene from Serratia strain SM6. These two genes are similar at both the DNA and protein sequence level. Expression of the protease gene in Escherichia coli was achieved by use of the lac promoter. This resulted in the production and excretion of an immunologically detectable but inactive protein of slightly higher molecular weight than that from Serratia. We introduced the cloned gene into previously described protease mutants. The observed pattern of protease expression suggested that these mutations fall into three classes.
利用粘质沙雷氏菌E-15株金属蛋白酶的DNA序列,我们从粘质沙雷氏菌SM6株中分离并测序了同源基因。这两个基因在DNA和蛋白质序列水平上都相似。通过使用lac启动子在大肠杆菌中实现了蛋白酶基因的表达。这导致产生并分泌出一种免疫可检测但无活性的蛋白质,其分子量略高于粘质沙雷氏菌产生的蛋白质。我们将克隆基因导入先前描述的蛋白酶突变体中。观察到的蛋白酶表达模式表明这些突变可分为三类。