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牙龈卟啉单胞菌编码蛋白酶活性的prtT基因的分离与鉴定。

Isolation and characterization of the Porphyromonas gingivalis prtT gene, coding for protease activity.

作者信息

Otogoto J, Kuramitsu H K

机构信息

Department of Pediatric Dentistry, University of Texas Health Science Center, San Antonio 78284-7888.

出版信息

Infect Immun. 1993 Jan;61(1):117-23. doi: 10.1128/iai.61.1.117-123.1993.

DOI:10.1128/iai.61.1.117-123.1993
PMID:8093357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC302695/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/e5b1da059dd5/iai00013-0144-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/f4987e018b37/iai00013-0140-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/cf7f66206b72/iai00013-0144-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/17a091a84f2a/iai00013-0144-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/e5b1da059dd5/iai00013-0144-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/f4987e018b37/iai00013-0140-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/cf7f66206b72/iai00013-0144-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/17a091a84f2a/iai00013-0144-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5374/302695/e5b1da059dd5/iai00013-0144-c.jpg

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本文引用的文献

1
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Oral Microbiol Immunol. 1987 Jun;2(2):77-81. doi: 10.1111/j.1399-302x.1987.tb00294.x.
2
Electrophoretic analysis of plasminogen activators in polyacrylamide gels containing sodium dodecyl sulfate and copolymerized substrates.在含有十二烷基硫酸钠和共聚底物的聚丙烯酰胺凝胶中对纤溶酶原激活剂进行电泳分析。
Anal Biochem. 1980 Feb;102(1):196-202. doi: 10.1016/0003-2697(80)90338-3.
3
Degradation of immunoglobulins A2, A2, and G by suspected principal periodontal pathogens.
利用pPGIVET系统鉴定和检测牙龈卟啉单胞菌的毒力基因
Infect Immun. 2002 Feb;70(2):928-37. doi: 10.1128/IAI.70.2.928-937.2002.
4
Transposition of the endogenous insertion sequence element IS1126 modulates gingipain expression in Porphyromonas gingivalis.内源性插入序列元件IS1126的转位调节牙龈卟啉单胞菌中牙龈蛋白酶的表达。
Infect Immun. 1999 Oct;67(10):5012-20. doi: 10.1128/IAI.67.10.5012-5020.1999.
5
Molecular mechanism for the spontaneous generation of pigmentless Porphyromonas gingivalis mutants.牙龈卟啉单胞菌无色素突变体自发产生的分子机制。
Infect Immun. 1999 Sep;67(9):4926-30. doi: 10.1128/IAI.67.9.4926-4930.1999.
6
Life below the gum line: pathogenic mechanisms of Porphyromonas gingivalis.龈下生活:牙龈卟啉单胞菌的致病机制
Microbiol Mol Biol Rev. 1998 Dec;62(4):1244-63. doi: 10.1128/MMBR.62.4.1244-1263.1998.
7
Regulation of protease expression in Porphyromonas gingivalis.牙龈卟啉单胞菌中蛋白酶表达的调控
Infect Immun. 1998 Nov;66(11):5232-7. doi: 10.1128/IAI.66.11.5232-5237.1998.
8
Role of Arg-gingipain A in virulence of Porphyromonas gingivalis.精氨酸牙龈蛋白酶A在牙龈卟啉单胞菌毒力中的作用。
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9
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疑似主要牙周病原体对免疫球蛋白A2、A2和G的降解作用。
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4
Black-pigmented Bacteroides species, Capnocytophaga species, and Actinobacillus actinomycetemcomitans in human periodontal disease: virulence factors in colonization, survival, and tissue destruction.人类牙周病中的黑色普氏菌属、二氧化碳嗜纤维菌属和伴放线放线杆菌:定植、存活及组织破坏中的毒力因子
J Dent Res. 1984 Mar;63(3):412-21. doi: 10.1177/00220345840630031101.
5
The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.pUC质粒,一种源自M13mp7的用于插入诱变和使用合成通用引物进行测序的系统。
Gene. 1982 Oct;19(3):259-68. doi: 10.1016/0378-1119(82)90015-4.
6
Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing.用核酸外切酶III进行单向消化可为DNA测序创建靶向断点。
Gene. 1984 Jun;28(3):351-9. doi: 10.1016/0378-1119(84)90153-7.
7
Characterization of a trypsin-like protease from the bacterium Bacteroides gingivalis isolated from human dental plaque.从人类牙菌斑中分离出的牙龈拟杆菌中一种类胰蛋白酶的特性研究
Arch Oral Biol. 1984;29(7):559-64. doi: 10.1016/0003-9969(84)90078-5.
8
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
9
The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites.大肠杆菌16S核糖体RNA的3'末端序列:与无义三联体及核糖体结合位点的互补性
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10
Isolation and characterization of a protease from Bacteroides gingivalis.牙龈拟杆菌中一种蛋白酶的分离与鉴定
Infect Immun. 1987 Mar;55(3):716-20. doi: 10.1128/iai.55.3.716-720.1987.