SR System Biology Research Group
The final goal of this research project is the understanding of all fundamental biological phenomena in a cell based on three-dimensional structure and function of all molecules. As a model organism for the structural and functional studies, an extremely thermophilic bacterium, Thermus thermophilus HB8, is very promising, because of the small genome size (2 Mbp), the availability of genetic tools for functional analysis, and the thermostability of its proteins. Using the protein structural information, this research group aims to reveal the functional information on a genome-wide scale by analyzing mRNA expression (transcriptomics), protein expression (proteomics) and metabolite dynamics (metabolomics). We use imaging technologies of SPring-8 and SACLA, and aim to establish the next basis of the prediction of the biological responses.
- Whole-Cell Project of a Model Organism, Thermus thermophilus HB8.
- Cell imaging / Biomolecular imaging, based on the synchrotoron and XFEL technologies.
- System biological analyses of anti-virus: CRISPR/Cas, transcription, Protein synthesis, and DNA repair systems in the cell.
- Functional identification of unknown functional protein (gene).
- RIKEN SPring-8 Center Website_Laboratories Page

- Structual-Biological Whole Cell Project Page

- DNA BANK Page

- November 18, 2008
- Elucidation of the regulatory mechanism of DNA recombination inducing genomic transformation, by controlling definitive choice to induce evolutional or non-evolutional transformation
- August 28, 2008
- Finding a new transcription factor from high temperature thermophilic bacteria, whicn functions when faced with a life crisis
- May 27, 2008
- Efficient protein three dimensional structure analysis in the world's top speed assisted by three types of automated crystallization robots, supporting the progress of the Structural-Biological Whole Cell Project.
- Yamamoto, T., Iino, H., Kim, K., Kuramitsu, S., and Fukui, K.:
"Evidence for ATP-dependent Structural Rearrangement of Nuclease Catalytic Site in DNA Mismatch Repair Endonuclease MutL"
J. Biol. Chem., 286, 41636-41646 (2011). - Agari, Y., Sakamoto, K., Tamakoshi, M., Oshima, T., Kuramitsu, S., Shinkai, A.:
"Transcription profile of Thermus thermophilus CRISPR systems after phage infection."
J. Mol. Biol., 395, 270-281 (2010). - Sakamoto, K., Agari, Y., Agari, K., Yokoyama, S., Kuramitsu, S., Shinkai, A.:
"X-ray crystal structure of a CRISPR-associated RAMP superfamily protein, Cmr5, from Thermus thermophilus HB8."
Proteins, 75, 528-532 (2009). - Kondo, N., Ebihara, A., Ru, H., Kuramitsu, S., Iwamoto, A., Rao, Z., and Matsuda, Z.:
"Thermus thermophilus-Derived Protein Tags That Aid in Preparation of Insoluble Viral Proteins."
Anal. Biochem. 385, 278-285 (2009). - Kondo, N., Nishikubo, T., Wakamatsu, T., Ishikawa, H., Nakagawa, N., Kuramitsu, S., and Masui, R.:
"Insights into Different Dependence of dNTP Triphosphohydrolase on Meta Ion Species from Intracellular Ion Concentrations in Thermus thermophilus."
Extremophiles 12, 217-223 (2008). - Agari, Y., Yokoyama, S., Kuramitsu, S., Shinkai, A.:
"X-ray crystal structure of a CRISPR-associated protein, Cse2, from Thermus thermophilus HB8."
Proteins, 73, 1063-1067 (2008). - Fukui, K., Takahata, Y., Nakagawa, N., Kuramitsu, S., and Masui, R.:
"Analysis of a Nuclease Activity of Catalytic Domain of Thermus thermophilus MutS2 by High-Accuracy Mass Spectrometry."
Nucleic Acids Res. 35, e100 (2007). - Mitani, Y., Lezhava, A., Kawai, Y., Kikuchi, T., Oguchi-Katayama, A., Kogo, Y., Itoh, M., Miyagi, T., Takakura, H., Hoshi, K., Kato, C., Arakawa, T., Shibata, K., Fukui, K., Masui, R., Kuramitsu, S., Kiyotani, K., Chalk, A., Tsunekawa, K., Murakami, M., Kamataki, T., Oka, T., Shimada, H., Cizdziel, P. E., and Hayashizaki, Y.:
"Rapid SNP Diagnostics Using Asymmetric Isothermal Amplification and A New Mismatch-Suppression Technology."
Nat. Methods 4, 257-262 (2007). - Hashimoto, Y., Yano, T., Kuramitsu, S., and Kagamiyama, H.:
"Disruption of Thermus thermophilus Genes by Homologous Recombination Using A Thermostable Kanamycin-Resistant Marker."
FEBS Lett. 506, 231-234 (2001). - Yokoyama, S., Hirota, H., Kigawa, T., Yabuki, T., Shirouzu, M., Terada, T., Ito, Y., Matsuo, Y., Kuroda, Y., Nishimura, Y., Kyogoku, Y., Miki, K., Masui, R., and Kuramitsu, S.:
"Structural Genomics Projects in Japan."
Nature Struct. Biol. 7, 943-945 (2000).
Principal Investigator
- Seiki KURAMITSU
- Group Director
| Functomics Integration Research Team | Seiki KURAMITSU (D.Sci.) |
| Functomics Biology I Research Team | Akeo SHINKAI (Ph.D.) |
| Functomics Biology II Research Team | Yoshitaka BESSHO (Ph.D.) |

