Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Nobuichi Goto"'
Autor:
Takeshi Igarashi, Hidetoshi Arakawa, Koji Karasawa, Masako Maeda, Shigeya Suzuki, Nobuichi Goto
Publikováno v:
Analytical Biochemistry. 333:296-302
We developed a novel bioluminescent assay for detection of pyrophosphate in polymerase chain reaction (PCR) product. The principle of this method is as follows: pyrophosphate released by PCR is converted to adenosine 5'-triphosphate (ATP) by pyruvate
Publikováno v:
Oral Microbiology and Immunology. 19:102-105
In order to clarify the role that sortase (SrtA) plays in anchoring dextranase (Dex) to the cell wall of Streptococcus mutans, both Dex- and SrtA- mutants were constructed by insertional inactivation of the respective genes. Western blot analysis wit
Publikováno v:
Letters in Applied Microbiology. 35:223-227
Aims: To examine the dextran-binding domain of the dextranase (Dex) of Streptococcus mutans. Methods and Results: Deletion mutants of the Dex gene of Strep. mutans were prepared by polymerase chain reaction and expressed in Escherichia coli cells. Bi
Publikováno v:
Oral Microbiology and Immunology. 17:193-196
Dextranase (Dex) is an enzyme that hydrolyzes glucan, a polymer of glucose synthesized from sucrose by glucosyltransferases (GTFs). By comparing amino acid sequences of Dexs and GTFs, we found that the Dex enzymes of Streptococcus mutans, Streptococc
Publikováno v:
Journal of Microbiological Methods. 46:99-105
A pair of polymerase chain reaction (PCR) primers was designed on the basis of the nucleotide sequence homology of dextranase genes (dex) of Streptococcus mutans, S. sobrinus and S. downei. The primer pair amplified a 530-bp DNA fragment on the dex g
Publikováno v:
Oral Microbiology and Immunology. 15:360-364
An oral parasite Trichomonas tenax ATCC 30207 synthesizes and secretes various proteinases. By gelatin-SDS-PAGE, we found five proteinases bands (30, 37, 46, 51 and 60 kDa) in cell lysate and four bands (37, 45, 52 and 60 kDa) in culture filtrate. Th
Publikováno v:
Oral Microbiology and Immunology. 14:233-237
Three DNA fragments (SSB-1, -2 and -3) in the dextranase gene (dex) of Streptococcus sobrinus were amplified by polymerase chain reaction and used as DNA probes. The probes were examined for the specificity and the sensitivity of hybridization with D
Publikováno v:
Oral Microbiology and Immunology. 13:382-386
Thirty-one strains of 23 gram-negative oral bacterial species were examined for dextran-degrading activity on agar plates containing blue dextran. One strain each of Capnocytophaga ochracea, Capnocytophaga sputigena, Prevotella loescheii, Prevotella
Publikováno v:
Journal of Microbiological Methods. 34:81-88
Polymerase chain reaction (PCR) primers for dextranase genes ( dex ) were designed for rapid identification of oral streptococci. The primers specifically amplified a 1.2-kb DNA fragment in dex of the oral streptococcal species: Streptococcus mutans
Autor:
Takashi Miyazaki, Takeshi Igarashi, Teruo Toko, Teuku Syafiuddin, Nobuichi Goto, Hisashi Hisamitsu, Akihiro Fujishima
Publikováno v:
Biomaterials. 18:1051-1057
Class V cavities were prepared and restored with resin composite containing antibacterial filler powder (Apacider-AW, Ap-AW) using experimental restorations. The restored teeth were incubated in vitro with the cariogenic bacteria Streptococcus mutans