Riffkin M C, Focareta A, Edwards R D, Stewart D J, Kortt A A
Division of Animal Health, CSIRO, Parkville, Victoria, Australia.
Gene. 1993 Dec 31;137(2):259-64. doi: 10.1016/0378-1119(93)90017-w.
The acidic protease V5-encoding gene (aprV5) from Gram- Dichelobacter nodosus virulent strain 198 was isolated from a cosmid bank by activity screening and sequenced. The 2371-bp nucleotide (nt) sequence contained an open reading frame coding for a protein precursor of 595 amino acid (aa) residues composed of a signal peptide, a pro-region, a mature active protease of 347 aa and a C-terminal extension region of 120 aa. The deduced aa sequence of the pre-pro-mature protease regions showed about 65% similarity to that of D. nodosus basic protease while the C-terminal extension region showed only about 26% similarity. The aprV5 gene, without its C-terminal extension region, was cloned and expressed in Escherichia coli. The acidic protease B5-encoding gene (aprB5) from non-virulent strain 305 was also cloned and sequenced. The aprB5 nt sequence showed 99% homology to that of aprV5 with two single-aa changes occurring in the precursor.
通过活性筛选从一个黏粒文库中分离出了来自革兰氏阴性的结节双歧杆菌强毒株198的酸性蛋白酶V5编码基因(aprV5),并进行了测序。2371个碱基对(bp)的核苷酸序列包含一个开放阅读框,编码一个由595个氨基酸(aa)残基组成的蛋白质前体,该前体由一个信号肽、一个前肽区、一个347个aa的成熟活性蛋白酶和一个120个aa的C端延伸区组成。前体-成熟蛋白酶区域推导的aa序列与结节双歧杆菌碱性蛋白酶的序列显示出约65%的相似性,而C端延伸区仅显示约26%的相似性。去除其C端延伸区的aprV5基因在大肠杆菌中进行了克隆和表达。来自无毒株305的酸性蛋白酶B5编码基因(aprB5)也进行了克隆和测序。aprB5核苷酸序列与aprV5的序列显示出99%的同源性,在前体中有两个单氨基酸变化。