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前田純夫の研究室へようこそ

過去の発表論文（抜粋）
  1. Genome-wide screening of Escherichia coli genes involved in execution and promotion of cell-to-cell transfer of non-conjugative plasmids: rodZ (yfgA) is essential for plasmid acceptance in recipient cells
    Kurono N, Matsuda A, Etchuya R, Sobue R, Sasaki Y, Ito M, Ando T, Maeda S, Biochem. Biophys. Res. Commun., 421: 119-123. (2012).
  2. Genome-wide screen for Escherichia coli genes involved in repressing cell-to-cell transfer of non-conjugative plasmids
    Matsuda A, Kurono N, Kawano C, Shirota K, Hirabayashi A, Horino M, Etchuya R, Sobue R, Sasaki Y, Miyaue S, Sekoguchi A, Sugiura C, Shibata Y, Ito M, Ando T, Maeda S, Biochem. Biophys. Res. Commun., 428: 445-450. (2012).
  3. Identification of a novel DNA element that promotes cell-to-cell transformation in Escherichia coli.
    Sobue R, Kurono N, Etchuya R, Maeda S, FEBS Letters., 585: 2223-2228. (2011).
  4. Cell-to-Cell Transformation in Escherichia coli: A Novel Type of Natural Transformation Involving Cell-Derived DNA and a Putative Promoting Pheromone.
    Etchuuya R, Ito M, Kitano S, Shigi F, Sobue R, Maeda, S., PLoS ONE, 6(1): e16355. doi:10.1371/journal.pone.0016355 (2011).
  5. Genome-Wide Screening of Escherichia coli Genes Involved in Execution and Promotion of Peptide-Pheromone-Regulated Natural Transformation.
    Kurono N, Matsuda A, Etchuuya R, Sobue R, Sasaki Y, Ando T, Ito M, Maeda S, Peptide Science 2010., 79. (2011).
  6. Genome-Wide Screening of Escherichia coli Genes Involved in Repression of Peptide-Pheromone-Regulated Natural Transformation.
    Matsuda A, Kurono N, Kawano C, Shirota K, Hirabayasi A, Horino M, Etchuuya R, Sobue R, Sasaki Y, Ando T, Ito M, Maeda S, Peptide Science 2010., 81. (2011).
  7. Horizontal transfer of non-conjugative plasmid in colony biofilm of Escherichia coli on food-based media.
    Ando T, Itakura S, Uchii K, Sobue R, Maeda S, World J Microbiol Biotechnol., 25: 1865-1869. (2009).
  8. Freeze-thaw-induced lateral transfer of non-conjugative plasmids by in situ transformation in Escherichia coli in natural waters and food extracts.
    Ishimoto Y, Kato S, Maeda S, World J Microbiol Biotechnol., 24: 2731-2735. (2008).
  9. Study on horizontal gene transfer in microbial biofilms
    Maeda, S.,IFO Research Communications., 21: 71-81 (2007).
  10. Horizontal Transfer of Nonconjugative Plasmids in a Colony Biofilm of Escherichia coli.
    Maeda, S., Ito, M., Ando, T., Ishimoto, Y., Fujisawa, Y., Takahashi, H., Matsuda, A., Sawamura, A., and Kato, S., FEMS Microbiol. Lett., 255, 115-120. (2006).
  11. Application and Examination of Phi29 DNA Polymerase-Amplified Rice DNA for PCR Analyses of Genetic Polymorphism.
    Ito, M., Inoue, S., and Maeda, S., DNA Polymorphism., 15, 299-303. (2007).
  12. Application and Examination of Phi29 DNA Polymerase-Amplified Human Buccal Cell DNA for PCR Analyses of Genetic Polymorphism.
    Ito, M., Inoue, S., and Maeda, S., DNA Polymorphism., 14, 46-51. (2006).
  13. Analysis of the Process of Social Acceptance of Genetically Modified Foods.
    Sakaitani, N. and Maeda, S., ResearchJournal of Living Science., 52, 27-38. (2005).
  14. A Simplified Methods for Detection of Human Genomic SNP by Cell-Direct PCR: A Test for ALDH2 Gene polymorphism.
    Ishimoto, Y. and Maeda, S., ResearchJournal of Living Science., 51, 1-5. (2004).
  15. Transformation of Escherichia coli on solid media.
    Maeda, S., Sawamura, A., and Matsuda, A., FEMS Microbiol. Lett., 236, 61-64. (2004).
  16. Competency Development of Escherichia coli in Foodstuffs.
    Maeda, S., Kakihara, N., and Koishi, Y., Microbes Environ., 18, 100-103. (2003).
  17. Purification and Characterization of an Extracellular Laccase of a Fungus (Family Chaetomiaceae) Isolated from Soil..
    Saito, T., Hong, P., Kato, K., Okazaki, M., Inagaki, H., Tanaka, K, Takada, M., Maeda, S., Yokogawa, Y. Enzyme Microbial Technology., 33, 520-526. (2003).
  18. Spatial Distribution of mDLG6 mRNA in Embryonic and Adult Mouse Brain.
    Inagaki, H., Tanaka, K, Takada, M., Maeda, S., Ichihara, S., Saito, T. Cell Biol Int., 26, 635-640. (2002).
  19. Mechanisms of Active Cell Death in Isolated Hepatocytes.
    Maeda, S., The Hepatocyte Review (Eds. Berry, M.N. & Edwards, T., Kluwer Academic Publishers), Chapter 18, pp281-300. (2000).
  20. Staurosporine Promotion of Formation of Continuous Monolayers of Primary Rat Hepatocytes by Improving Attachment and Spreading.
    Maeda, S., Lin, K.H., Inagaki, H., and Saito, T., Biosci. Biothech. Biochem., 64, 1985-1987. (2000).
  21. rDLG6: a Novel Homolog of Drosophila DLG Expressed in Rat Brain.
    Inagaki, H., Maeda, S., Lin, K.H., Shimizu, N., and Saito, T., Biochem. Biophys. Res. Commun., 265, 462-468. (1999).
  22. Inhibition of Mitochondrial Gene Expression by Antisense RNA of Mitochondrial Transcription Factor A (mtTFA).
    Inagaki, H., Kitano, S., Lin, K.H., Maeda, S., and Saito, T., Biochem. Mol. Biol. International., 45, 567-573. (1998).
  23. Promotive Effect of DMSO on TGF-beta1-Induced Apoptosis in Primary Culture of Rat Hepatocytes.
    Maeda, S., Miyazawa, A., Lin, K.H., Inagaki, H., and Saito, T., J. Biochem. Mol. Biol. Biophys., 1, 117-124. (1997).
  24. Long-Term Culture of Rat Hepatocytes on Heparin- or Lambda Carrageenan- containing Collagen Gels.
    Lin, K.H., Maeda, S., Inagaki, H., and Saito, T., Biosci. Biothech. Biochem., 61, 971-974. (1997).
  25. Induction of Apoptosis in Primary Culture of Rat Hepatocytes by Protease Inhibitors.
    Maeda, S., Lin, K.H., Inagaki, H., and Saito, T., Biochem. Mol. Biol. International., 39, 447-453. (1996).
  26. Osteonectin Gene Expression in Fibrotic Liver.
    Inagaki, H., Lin, K.H., Maeda, S., and Saito, T., Life Sciences, 58, 927-934. (1996).
  27. DNA Fragmentation Induced in High-Cell-Density Culture of Primary Rat Hepatocytes Is an Active Process Dependent on Energy Availability, Gene Expression, and Calmodulin.
    Maeda, S., Suzuki, A., Lin, K.H., Inagaki, H., and Saito, T., J. Biochem., 118, 1161-1165. (1995).
  28. Albumin Synthesis by Rat Hepatocytes Cultured on Collagen Gels Is Sustained Specifically by Heparin.
    Lin, K.H., Hino, H., Maeda, S., Inagaki, H., Valiakhmetov, A.J., and Saito, T., Exp. Cell Res., 218, 717-721. (1995).
  29. Long-Term Maintenance of Liver-Specific Functions in Three-Dimensional Culture of Adult Rat Hepatocytes with a Porous Gelatin Sponge Support.
    Lin, K.H., Maeda, S., and Saito, T., Biotech. Appl. Biochem., 21, 19-27. (1995).
  30. Inhibition by Retinoic Acid of Albumin and DNA Synthesis in Adult Rat Hepatocytes.
    Lin, K.H., Maeda, S., Koga, N., and Saito, T., Biosci. Biotech. Biochem., 58, 584-585. (1994).
  31. Immobilization and Characterization of a Thermostable beta-Galactosidase from a Thermophilic Anaerobe on a Porous Ceramic Support..
    Saito, T., Yoshida, Y., Kawashima, K., Lin, K.H., Maeda, S., and Kobayashi, T., Appl. Microbiol. Biotech., 40, 618-621. (1994).
  32. Cell Density-Dependent DNA Fragmentation and Its Suppression by Heparin in Primary Culture of Adult Rat Hepatocytes.
    Maeda, S., Kimura, H., Koga, N., Lin, K.H., and Saito, T., Biochem. Biophys. Res. Commun., 195, 270-275. (1993).
  33. Overproduction of Thermostable beta-Galactosidase in Escherichia coli, Its Purification and Molecular Structure.
    Saito, T., Kato, K., Maeda, S., Suzuki, T., Shiba, S., Iijima, S., and Kobayashi, T., J. Ferment. Bioeng., 74, 12-16. (1992).
  34. A Modified Cololimetric MTT Assay for Primary Cultured Hepatocytes : Application to Proliferation and Cytotoxicity Assays.
    Oka, M., Maeda,S., Koga, N., Kato, K., and Saito, T., Biosci. Biotech. Biochem., 56, 1472-1473. (1992).
  35. Activation of the Osmoregulated ompC Gene by the OmpR Protein in Escherichia coli : A Study Involving Synthetic OmpR-Binding Sequences.
    Maeda, S., Takayanagi, K., Nishimura, Y., Maruyama, T., Sato, K., and Mizuno, T., J. Biochem., 110, 324-327. (1991).
  36. Expression of micF Involved in Porin Synthesis in Escherichia coli: Two Distinct Cis-Acting Elements Respectively Regulate micF Expression Positively and Negatively.
    Takayanagi, K., Maeda, S., and Mizuno, T., FEMS Microbiol. Lett., 83, 39-44. (1991).
  37. Evidence for Multiple OmpR-Binding Sites in the Upstream Activation Sequence of the ompC Promoter in Escherichia coli : a Single OmpR-Binding Site Is Capable of Activating the Promoter.
    Maeda, S. and Mizuno, T., J. Bacteriol., 172, 501-503. (1990).
  38. Activation of the ompC Gene by the OmpR Protein in Escherichia coli : the Cis-Acting Upstream Sequence Can Function in Both Orientations with Respect to the Canonical Promoter.
    Maeda, S. and Mizuno, T., J. Biol. Chem., 263, 14629-14633. (1988).
  39. Stereospecific Positioning of the Canonical Promoter Is Required for Activation of the ompC Gene by a Positive Regulator, OmpR, in Escherichia coli.
    Maeda, S., Ozawa, Y., Mizuno, T., and Mizushima, S., J. Mol. Biol., 202, 433-441. (1988).

学会発表： 国内　　　：日本分子生物学会・日本生化学会・日本微生物生態学会　など
　　　　海外・国際：ASM Conference (2005, Canada), FEMS Congress (2006, Spain; 2011, Switzerland), IUBMB International Congress (2006, Kyoto),
　　　　　　　　　　IUMS Congress (2008, Turkey; 2011, Sapporo), International Peptide Symposium (2010, Kyoto), FoodMicro2012 (2012, Turkey) など

学外・公開講演：　バイオフィルム・遺伝子水平伝播（日本食品工業倶楽部、(財)発酵研究所、など）、遺伝子組換え食品（近畿農政局、滋賀県、生協、など）、

特許：　国内特許２件、米国・欧州特許２件

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Last Updated on March-22-2013