Pastar I, Fira D, Strahinić I, Krstić K, Begović J, Topisirović L, Jovanović G
Institute of Molecular Genetics and Genetic Engineering, Belgrade, Serbia.
Folia Microbiol (Praha). 2006;51(6):535-40. doi: 10.1007/BF02931617.
The region of the prtR gene coding for the active site of PrtR proteinase was detected in natural isolates of lactobacilli, previously determined as Lactobacillus rhamnosus. This region was present in all L. rhamnosus strains with proteolytic activity. The PCR primers used were constructed on the basis of the sequence of the catalytic domain of the prtR proteinase gene. These primers generated in colony-PCR procedure specific 611 1-bp product with DNA from natural isolates of L. rhamnosus. No PCR amplifications using these primers were obtained for closely related bacteria of genus Lactobacillus, regardless of their proteolytic activity. In addition, these primers could be used singly or in multiplex PCR together with the Lactobacillus genus-specific primers. Compared with the other proteinases within the genus Lactobacillus (PrtP, PrtB and PrtH) which retained the activity in cell-free proteinase extracts, PrtR proteinase showed proteolytic activity only under in vivo conditions (whole cells of the producing strains).
在先前鉴定为鼠李糖乳杆菌的乳酸杆菌自然分离株中,检测到编码PrtR蛋白酶活性位点的prtR基因区域。该区域存在于所有具有蛋白水解活性的鼠李糖乳杆菌菌株中。所用的PCR引物是根据prtR蛋白酶基因催化结构域的序列构建的。这些引物在菌落PCR程序中,能从鼠李糖乳杆菌自然分离株的DNA中产生特异性的611 bp产物。对于乳酸杆菌属的近缘细菌,无论其蛋白水解活性如何,使用这些引物均未获得PCR扩增产物。此外,这些引物可单独使用,也可与乳酸杆菌属特异性引物一起用于多重PCR。与在无细胞蛋白酶提取物中仍保持活性的乳酸杆菌属其他蛋白酶(PrtP、PrtB和PrtH)相比,PrtR蛋白酶仅在体内条件下(产生菌株的全细胞)显示蛋白水解活性。