Schad P A, Iglewski B H
Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, New York 14642.
J Bacteriol. 1988 Jun;170(6):2784-9. doi: 10.1128/jb.170.6.2784-2789.1988.
Pseudomonas aeruginosa PAO-E64 is a mutant which produces parental levels of elastase antigen but has no elastolytic activity at 37 degrees C. The lesion (lasA1) in PAO-E64 is not a mutation in the structural gene for P. aeruginosa elastase (P.A. Schad, R.A. Bever, T.I. Nicas, F. Leduce, L.F. Hanne, and B.H. Iglewski, J. Bacteriol. 169: 2691-2696, 1987). A 1.7-kilobase segment of DNA that complements the lasA1 lesion was sequenced. Computer analysis of the DNA sequence showed that it contained an open reading frame which encoded a 41,111-dalton protein. The lasA gene was expressed under an inducible PT-7 promoter, and a 40,000-dalton protein was detected in Escherichia coli lysates. The lasA protein was localized in the outer membrane fraction of E. coli. This lasA protein produced in E. coli activated the extracellular elastase produced by the P. aeruginosa mutant, PAO-E64.
铜绿假单胞菌PAO - E64是一种突变体,其产生的弹性蛋白酶抗原水平与亲本相同,但在37℃时没有弹性水解活性。PAO - E64中的病变(lasA1)不是铜绿假单胞菌弹性蛋白酶结构基因的突变(P.A. 沙德、R.A. 贝弗、T.I. 尼卡斯、F. 勒杜斯、L.F. 汉内和B.H. 伊格尔斯基,《细菌学杂志》169: 2691 - 2696, 1987)。对一个可弥补lasA1病变的1.7千碱基DNA片段进行了测序。对该DNA序列的计算机分析表明,它包含一个开放阅读框,编码一种41,111道尔顿的蛋白质。lasA基因在可诱导的PT - 7启动子下表达,在大肠杆菌裂解物中检测到一种40,000道尔顿的蛋白质。lasA蛋白定位于大肠杆菌的外膜部分。在大肠杆菌中产生的这种lasA蛋白激活了铜绿假单胞菌突变体PAO - E64产生的细胞外弹性蛋白酶。