Project/Area Number |
22592283
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Orthodontic/Pediatric dentistry
|
Research Institution | Osaka University |
Principal Investigator |
INAGAKI Satoko 大阪大学, 歯学部附属病院, 医員 (50527223)
|
Co-Investigator(Kenkyū-buntansha) |
OOSHIMA Takashi 大阪大学, 歯学研究科, 招聘教員 (80116003)
NAKANO Michiyo 岡山大学, 医歯薬学総合研究科, 教授 (30359848)
|
Project Period (FY) |
2010 – 2012
|
Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2010: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
Keywords | Streptococcus mutans / リコンビナーゼA / クオラムセンシング / バイオフィルム / Recombinase A / Glucosyltransferase / リコンビネーション / 耐酸性 / 臨床分離株 / う蝕 / グルコシルトランスフェラーゼ |
Research Abstract |
Streptococcus mutansproduces 3 types of glucosyltransferases (GTFs), whose cooperative action is essential for cellular adhesion, with the recombinase A (RecA) protein required for homologous recombination. Determination of the sequences of the gtfBand gtfCgenes showed that an approximately 3500-bp region was deleted in the smooth colonies of S. mutans. These results suggest that DNA recombination and phenotypic changes that occur through uptake of extracellular RecA may have a relationship with the signal transduction system involving biofilm formation in S. mutans.
|