| Project/Area Number |
09470472
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
矯正・小児・社会系歯学
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| Research Institution | The University of Tokushima |
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Principal Investigator |
NAKAMURA Ryo The University of Tokushima, School of Dentistry, Professor, 歯学部, 教授 (30034169)
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| Co-Investigator(Kenkyū-buntansha) |
MASUDA Kaname The University of Tokushima, School of Dentistry, Research Associate, 歯学部, 助手 (30243710)
YOSHIOKA Masami The University of Tokushima, School of Dentistry, Assistant Professor, 歯学部・附属病院, 講師 (90243708)
HINODE Daisuke The University of Tokushima, School of Dentistry, Associate Professor, 歯学部, 助教授 (70189801)
SHIMADA Junko The University of Tokushima, School of Dentistry, Assistant, 歯学部, 教務員 (10170945)
TANABE Shin-ichi The University of Tokushima, School of Dentistry, Research Associate, 歯学部, 助手 (40284301)
赤木 毅 徳島大学, 歯学部・附属病院, 助手 (50314878)
大塚 千亜紀 徳島大学, 歯学部, 助手 (00263848)
冨田 耕治 徳島大学, 歯学部, 助手 (10263849)
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| Project Period (FY) |
1997 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥13,900,000 (Direct Cost: ¥13,900,000)
Fiscal Year 1999: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 1998: ¥4,300,000 (Direct Cost: ¥4,300,000)
Fiscal Year 1997: ¥7,000,000 (Direct Cost: ¥7,000,000)
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| Keywords | Growth of Porphyromonas gingivalis / Arginine Carboxypeptidase / ATP production / Arginine deminase / Energy production / Heat-shock proteins / Self-defense system / Periodontopathogenicity / アルギミン・デイミナーゼ / Gro-EL様蛋白質 / DnaK様蛋白質 / アルギニン・カルボキシペプチダーゼ / アルギニン関連酵素 / 細胞毒性 / 歯周病原性 / Porphyromonas gingivalis |
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| Research Abstract |
Porphyromonas gingivalis (P.g.) predominantly consumes arginine in the anaerobic BHI-broth, suggesting that this amino acid could be the primary energy source. Arginine carboxypeptidase, which is one of enzymes to participate in releasing arginine from peptides, was isolated and purified from cytoplasm of P.g. cells. SDS-PAGE of the enzyme with 2-mercaptoethanol revealed the presence of three major bands of 42, 33 and 32kDa, of which 30 amino acid sequences at NHィイD22ィエD2-terminal were identical, YEWNAYPTYEAYISMMEEFQT-KYPSLXTXS. The open reading frame (ORF), suspected from the nucleotide sequences corresponding to the N-terminal amino acids on the data bases containing unfinished P.g. W83 genome, showed to include zinc-binding regions signature, suggesting a zinc carboxypeptidase. In order to release arginine from the inside of the peptides, this enzyme, which was determined as a exo-type of carboxypeptidase, could work in combination with the trypsin like enzyme (cystein protease), which is considered as the main periodontopathogen of this bacterium. In relation to the arginine consumption and energy production, cell extracts of P. g. clearly demonstrated enzyme activities for the arginine deminase pathway and the adenosine triphosphate production. Besides arginine catabolism, P. g. conserved the heat-shock protein and increased the synthesis after a thermal shock, suggesting the physiologic role to protect their own cells. These results show that P. g. possesses self-defense systems by consuming periodontal tissues in the deep anaerobic pockets and producing heat-shock proteins for the changes of their environments.
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