Otogoto J, Kuramitsu H K
Department of Pediatric Dentistry, University of Texas Health Science Center, San Antonio 78284-7888.
Infect Immun. 1993 Jan;61(1):117-23. doi: 10.1128/iai.61.1.117-123.1993.
The prtT gene, coding for trypsinlike proteolytic activity, has been isolated from Porphyromonas gingivalis ATCC 53977. This gene is present immediately downstream from the sod gene on a 5.9-kb DNA fragment from the organism isolated in Escherichia coli. The complete nucleotide sequence of the gene was determined, and the deduced amino acid sequence of the enzyme corresponds to a 53.9-kDa protein with an estimated pI of 11.85. Gelatin-sodium dodecyl sulfate-polyacrylamide gel electrophoresis zymography also indicated a similar molecular size for the protease. The enzyme was purified to near homogeneity following anion-exchange and gel-filtration chromatography. The purified enzyme also exhibited a single protein species with a size of approximately 53 kDa. Enzyme activity was strongly dependent upon the presence of reducing agents (dithiothreitol, cysteine, and 2-mercaptoethanol) and was also stimulated in the presence of calcium ions. A comparison of the properties of the prtT gene product with comparable parameters of proteases previously purified from different strains of P. gingivalis suggested that the cloned protease represents a previously uncharacterized enzyme.
编码类胰蛋白酶活性的prtT基因已从牙龈卟啉单胞菌ATCC 53977中分离出来。该基因位于从该生物体中分离出的、存在于大肠杆菌中的一个5.9 kb DNA片段上sod基因的紧邻下游。确定了该基因的完整核苷酸序列,推导的酶氨基酸序列对应于一个53.9 kDa的蛋白质,估计pI为11.85。明胶 - 十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳酶谱分析也表明该蛋白酶具有相似的分子大小。经过阴离子交换和凝胶过滤色谱后,该酶被纯化至接近均一。纯化后的酶也呈现出一种大小约为53 kDa的单一蛋白质。酶活性强烈依赖于还原剂(二硫苏糖醇、半胱氨酸和2 - 巯基乙醇)的存在,并且在钙离子存在时也受到刺激。将prtT基因产物的特性与先前从不同牙龈卟啉单胞菌菌株中纯化的蛋白酶的可比参数进行比较,表明克隆的蛋白酶代表一种以前未被表征的酶。