Papers - MIYAGAWA Atsushi

Division display >> /  All the affair displays  1 - 62 of about 62
  • Preparation of β-1, 3-glucan mimics via modification of polymer backbone, and evaluation of cytokine production using the polymer library in immune activation Reviewed International journal

    Miyagawa, A., Yamamoto, N., Ohno, A., Yamamura, H

    International Journal of Biological Macromolecules   264   130546   2024.04

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: doi.org/10.1016/j.ijbiomac.2024.130546

  • Molecular basis for bacterial N-glycosylation by a soluble HMW1C-like N-glycosyltransferase Reviewed International coauthorship International journal

    Beatriz Piniello, Javier Macías-León, Shun Miyazaki, Ana García-García, Ismael Compañón, Mattia Ghirardello, Víctor Taleb, Billy Veloz, Francisco Corzana, Atsushi Miyagawa, Carme Rovira, Ramon Hurtado-Guerrero

    Nature Communications   14   5785   2023.09

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: https://doi.org/10.1038/s41467-023-41238-1

    Other Link: https://www.nature.com/articles/s41467-023-41238-1

  • Identification of a tomato UDP-arabinosyltransferase for airborne volatile reception Reviewed International journal

    Koichi Sugimoto, Eiichiro Ono, Tamaki Inaba, Takehiko Tsukahara, Kenji Matsui, Manabu Horikawa, Hiromi Toyonaga, Kohki Fujikawa, Tsukiho Osawa, Shunichi Homma, Yoshikazu Kiriiwa, Ippei Ohmura, Atsushi Miyagawa, Hatsuo Yamamura, Mikio Fujii, Rika Ozawa, Bunta Watanabe, Kenji Miura, Hiroshi Ezura, Toshiyuki Ohnishi, Junji Takabayashi

    14   677   2023.02

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: https://doi.org/10.1038/s41467-023-36381-8

    Other Link: https://www.nature.com/articles/s41467-023-36381-8

  • One-step Synthesis of Sugar Nucleotides Reviewed International journal

    Atsushi Miyagawa, Sanami Toyama, Ippei Ohmura, Shun Miyazaki, Takeru Kamiya, Hatsuo Yamamura

    The Journal of Organic Chemistry   85 ( 23 )   15645 - 15651   2020.11

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society  

    DOI: https://doi.org/10.1021/acs.joc.0c01943

  • Preparation of Amylose-Mimicking Polymers for thePurification of Maltose-Binding Protein

    63   1614 - 1627   2025.02

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/pol.20241130

  • One-step synthesis of sugar nucleotides under optimized conditions Reviewed

    Kota Fujihara,Hatsuo Yamamura, Atsushi Miyagawa

    Synthetic Communications   54 ( 14 )   1245 - 1251   2024.07

     More details

    Authorship:Last author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: https://doi.org/10.1080/00397911.2024.2380063

  • Amphiphilic cyclodextrin derivatives with antibacterial activity: chemical mutation and structure–activity relationship Reviewed

    Hatsuo Yamamura, Ayame Kato, Eri Yamada, Hisato Kato, Takashi Katsu, Kazufumi Masuda, Kayo Osawa, Atsushi Miyagawa

    New Journal of Chemistry   48   12355 - 12361   2024.06

     More details

    Authorship:Last author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/D4NJ01874E

  • 安全で抗菌性に優れた新規オリゴ糖誘導体—防腐効果のある化粧品原料の開発— Reviewed

    小見宏幸,髙田健太,竹内彩乃,村上栞菜,宮川 淳,山村初雄

    日本香粧品学会誌   48 ( 2 )   82 - 88   2024.06

     More details

    Language:Japanese   Publishing type:Research paper (scientific journal)  

  • Facile synthesis of β-1,3-glucan disaccharides using acyl protected glycosyl donors and acceptors prepared from 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose Invited Reviewed

    Atsushi Miyagawa, Ryusuke Tomita, Hatsuo Yamamura

    TRENDS IN ORGANIC CHEMISTRY   24   69 - 78   2024.05

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

  • Synthesis of cyclodextrin dimers via Diels–Alder reaction Reviewed International journal

    Atsushi Miyagawa,Takuya Hasegawa, Hatsuo Yamamura

    Synthetic Communications   53 ( 22 )   1878 - 1885   2023.09

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: https://doi.org/10.1080/00397911.2023.2254427

  • Anti-bacterial β-cyclodextrin derivatives inspired by the antimicrobial peptide polymyxin in order to better understand the role of single hydrophobic chain tail in selective anti-bacterial activity Reviewed International journal

    Hatsuo Yamamura, Masashi Owaki, Kana Isshiki, Yukari Ishihara, Hisato Kato, Takashi Katsu, Kazufumi Masuda, Kayo Osawac, Atsushi Miyagawa

    New Journal of Chemistry   47   10921 - 10929   2023.04

     More details

    Authorship:Last author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: https://doi.org/10.1039/D3NJ01028G

  • Synthesis of antimicrobial polymers with mannose residues for binding to the FimH adhesin of Escherichia coli Reviewed International journal

    Atsushi Miyagawa, Shinya Ohno, Hatsuo Yamamura

    61 ( 4 )   277 - 288   2023.02

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:John Wiley & Sons, Inc.  

    DOI: https://doi.org/10.1002/pol.20220540

  • Protecting-group-free glycosylation of phosphatidic acid in aqueous media Reviewed International journal

    Koki Kano, Nozomi Ishii, Atsushi Miyagawa, Hiroaki Takeda, Yoshio Hirabayashi, Hiroyuki Kamiguchi, Peter Greimel, Ichiro Matsuo

    Organic & Biomolecular Chemistry   21   2138 - 2142   2023.02

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: https://doi.org/10.1039/D2OB02173K

  • UDP-glucose, cereblon-dependent proinsulin degrader Reviewed International journal

    Jaeyong Cho, Atsushi Miyagawa, Kazuki Yamaguchi, Wakana Abe, Yoji Tsugawa, Hatsuo Yamamura, Takeshi Imai

    Scientific Reports   12   14568   2022.08

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1038/s41598-022-18902-5

  • UDP-Glucose: A Cereblon-Dependent Glucokinase Protein Degrader Reviewed International journal

    Jaeyong Cho, Atsushi Miyagawa, Kazuki Yamaguchi, Wakana Abe, Yoji Tsugawa, Hatsuo Yamamura, Takeshi Imai

    International Journal of Molecular Sciences   23 ( 16 )   9094   2022.08

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.3390/ijms23169094

  • Synthesis of UDP-glucose with 1,2-trans glycoside in a one-step reaction Reviewed International journal

    Atsushi Miyagawa, Saki Kamikawa, Shun Miyazaki, Takeru Kamiya, HatsuoYamamura

    Tetrahedron Letters   103   153995   2022.07

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.tetlet.2022.153995

  • Antibacterial Activity of Membrane-permeabilizing Bactericidal Cyclodextrin Derivatives Reviewed International journal

    Yamamura, Hatsuo; Hagiwara, Tatsuya; Hayashi, Yuma; Osawa, Kayo; Kato, Hisato; Katsu, Takashi; Masuda, Kazufumi; Sumino, Ayumi; Yamashita, Hayato; Jinno, Ryo; Abe, Masayuki; Miyagawa, Atsushi

    ACS Omega   6 ( 47 )   31831 - 31842   2021.11

     More details

    Authorship:Last author   Language:English   Publishing type:Research paper (scientific journal)  

  • Antimicrobial activities of amphiphilic cationic polymers and their efficacy of combination with novobiocin Reviewed International journal

    Atsushi Miyagawa, Shinya Ohno, Tomohiko Hattori, Hatsuo Yamamura

    Journal of Biomaterials Science, Polymer Edition   2021.10

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1080/09205063.2021.1985243

  • N, N-Bis (hexyl α-d-acetylmannosyl) Acrylamide Invited Reviewed International journal

    Atsushi Miyagawa, Shinya Ohno, Hatsuo Yamamura

    Molbank   3   M1255   2021.07

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.3390/M1255

  • Synthesis of β-1,3-glucan mimics by β-1,3-glucan trisaccharyl monomer polymerization Reviewed International journal

    Atsushi Miyagawa, Hatsuo Yamamura

    Carbohydrate polymers   227   115105   2019.09

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • Gramicidin S-inspired antimicrobial cyclodextrin to disrupt gram-negative and gram-positive bacterial membranes Reviewed International journal

    Hatsuo Yamamura, Kana Isshiki, Yusuke Fujita, Hisato Kato, Takashi Katsu, Kazufumi Masuda, Kayo Osawa, Atsushi Miyagawa

    MedChemComm   10 ( 8 )   1432 - 1437   2019.07

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/c9md00229d

  • Development of New Antimicrobial Agents from Cationic PG-Surfactants Containing Oligo-Lys Peptides Reviewed International journal

    Ryosuke Kimura, Masahide Shibata, Shuhei Koeda, Atsushi Miyagawa, Hatsuo Yamamura, Toshihisa Mizuno

    Bioconjugate Chemistry   2018.10

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Transglycosylation Activity of Catalytic Domain Mutant of Endo-1,3-β-glucanase from Cellulosimicrobium cellulans Reviewed International journal

    Yoshiji Hantani, Shoko Motoki, Atsushi Miyagawa, Hatsuo Yamamura, Masayuki Oda

    Protein and Peptide Letters   25 ( 8 )   734 - 739   2018.10

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Membrane-active antimicrobial poly(amino-modified alkyl) β-cyclodextrins synthesized via click reactions Reviewed International journal

    Hisato Kato, Takashi Katsu, Kazufumi Masuda, Koichi Tanimoto, Haruyoshi Tomita, Atsushi Miyagawa

    Med. Chem. Commun.   9   509 - 518   2018.02

     More details

    Language:English   Publishing type:Research paper (scientific journal)   Publisher:The Royal Society of Chemistry  

    DOI: 10.1039/C7MD00592J

  • Syntheses and structure–membrane active antimicrobial activity relationship of alkylamino-modified glucose, maltooligosaccharide, and amylose Reviewed International journal

    Hatsuo Yamamura, Takahiro Mabuchi, Tomoki Ishida, Atsushi Miyagawa

    Chemical Biology & Drug Design   90   1012 - 1018   2017.11

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1111/cbdd.12989

  • Chemical synthesis and isolation of UDP-2-deoxy glucose and galactose Reviewed International journal

    Atsushi Miyagawa, Shunya Takeuchi, Shinji Itoda, Sanami Toyama, Kenta Kurimoto, Hatsuo Yamamura, Yukishige Ito

    Synthetic Communications   46 ( 22 )   1790 - 1795   2016.08

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1080/00397911.2016.1227849

  • Aglycone Specificity of Endo-β-1,3-Glucanase Reviewed International journal

    Atsushi Miyagawa, Takahiro Yamaguchi, Yoichi Tanabe,Masayuki Oda, Hatsuo Yamamura

    JSM Chemistry   4 ( 2 )   1026   2016.07

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • 2II-VII, 3I-VII, 6I-VII-Icosa-O-acetyl-2I-deoxy-cyclomaltoheptaose Invited Reviewed International journal

    Atsushi Miyagawa, Kazuki Kano, Aya Yoshida, Hatsuo Yamamura

    Molbank   2016 ( 2 )   M900   2016.05

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • Rule of Hydrophobicity/Hydrophilicity Balance in Membrane-Disrupting Antimicrobial Activity of Polyalkylamino Cyclodextrins Synthesized via Click Chemistry Reviewed International journal

    Yamamura,H., Miyagawa, A., Sugiyama, H., Murata

    ChemistrySelect   2016.03

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Selective Deprotection of Trityl Group on Carbohydrate by Microflow Reaction Inhibiting Migration of Acetyl Group Reviewed

    Atsushi Miyagawa, Ryusuke Tomita, Kenta Kurimoto, Hatsuo Yamamura

    Synthetic Communications   2016.02

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • Sialylation with systematically protected allyl galactoside acceptors using sialyl phosphate donors Reviewed

    Kenta Kurimoto, Hatsuo Yamamura, Atsushi Miyagawa

    Tetrahedron Letters   2016.02

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • Functionalization of Aglycones on Sialoside Derivatives to Generate Precursors for Biological Applications Reviewed

    Kenta Kurimoto, Hatsuo Yamamura, Atsushi Miyagawa

    Chemistry Letters   45 ( 2 )   128 - 130   2015.11

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • Synthesis of Branched Tetrasaccharide Derivatives of Schizophyllan-like beta-Glucan Reviewed

    Atsushi Miyagawa, Tomoka Matsuda, Hatsuo Yamamura

    JOURNAL OF CARBOHYDRATE CHEMISTRY   34 ( 5 )   215 - 246   2015.06

     More details

    Language:English   Publishing type:Research paper (scientific journal)   Publisher:TAYLOR & FRANCIS INC  

    GRAPHICAL ABSTRACT
    [GRAPHICS]
    Branched tetrasaccharide derivatives as the repeating units of schizophyllan were synthesized using a common intermediate that had different protecting groups on the hydroxyl groups. Accordingly, beta-1,3-disaccharide acceptors were efficiently glycosylated in a stepwise manner using monosaccharide donors to construct the branched tetrasaccharides. As a result, oligosaccharides with an internal branch rather than a branch on the terminal residue suitable for the synthesis of branched beta-glucan were obtained.

    DOI: 10.1080/07328303.2015.1044754

    Web of Science

    researchmap

  • Synthesis of Branched Tetrasaccharide Derivatives toward the Synthesis of Schizophyllan-like β-Glucan Reviewed

    Atsushi Miyagawa, Tomoka Matsuda, Hatsuo Yamamura

    Journal of Carbohydrate Chemistry   2015.05

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • Polysulfonylated cyclodextrins. Part 14. Structural validation of tris-and pentakis(6-O-mesitylsulfony)cyclomaltooctaose isomers by H-1-NMR spectrometry Reviewed

    Hatsuo Yamamura, Mutsumi Watanabe, Sho Kawahara, Atsushi Miyagawa, Masao Kawai

    MAGNETIC RESONANCE IN CHEMISTRY   53 ( 3 )   237 - 243   2015.03

     More details

    Language:English   Publishing type:Research paper (scientific journal)   Publisher:WILEY-BLACKWELL  

    DOI: 10.1002/mrc.4165

    Web of Science

    researchmap

  • Comprehensive syntheses of sialyl galactoside regioisomers Reviewed

    Kenta Kurimoto, Hatsuo Yamamura, Atsushi Miyagawa

    Glycobiology   2014.11

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (international conference proceedings)  

  • Synthetic β-1,3-Oligoglucans as Probes to Study for Hydrolysis and Recognition of Endo-β-1,3-Glucanase Reviewed

    Atsushi Miyagawa, Masayuki Oda, Hatsuo Yamamura

    Glycobiology   2014.11

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (international conference proceedings)  

  • Chemical approach for the syntheses of GM4 isomers with sialic acid to non-natural linkage positions on galactose Reviewed

    Kenta Kurimoto, Hatsuo Yamamura, Atsushi Miyagawa

    Carbohydrate Research   40 ( 12 )   39 - 50   2014.10

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • Polysulfonylated cyclodextrins. Part 14. Structural validation of tris- and pentakis(6-O-mesitylsulfony)cyclomaltooctaose isomers by 1H-NMR spectrometry Reviewed

    Hatsuo Yamamura, Mutsumi Watanabe, Sho Kawahara, Atsushi Miyagawa, Masao Kawai

    Magnetic Resonance in Chemistry   2014.10

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Synthesis of antimicrobial cyclodextrins bearing polyarylamino and polyalkylamino groups via click chemistry for bacterial membrane disruption Reviewed

    Hatsuo Yamamura、Yuuki Sugiyama、Kensuke Murata、Takanori Yokoi、Ryuji Kurata、Atsushi Miyagawa、 Kenji Sakamoto、Keiko Komagoe、Tsuyoshi Inoue、Takashi Katsu

    Chemical Communications   2014.02

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Unique, Fast, and All-or-none Click Reaction on Cyclodextrin and Amylose Reviewed

    Hatsuo Yamamura,Kyohei Shimohara,Ryuji Kurata,Yusuke Fujita,Kensuke Murata,Takaaki Hayashi,Atsushi Miyagawa

    Chemistry Letters   42 ( 6 )   643 - 645   2013.06

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Mimicking an antimicrobial peptide polymyxin B by use of cyclodextrin Reviewed

    Hatsuo Yamamura, Ken Suzuki, Kazuma Uchibori, Atsushi Miyagawa, Masao Kawai, Chie Ohmizo, Takashi Katsu

    Chemical Communications   48   892 - 894   2011.12

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/C1CC16369H

    Other Link: http://pubs.rsc.org/en/content/articlehtml/2012/cc/c1cc16369h

  • Promiscuous activity of ER glucosidase II discovered through donor specificity analysis of UGGT Reviewed

    Atsushi Miyagawa et al.

    Biochemical and Biophysical Research Communications   403 ( 3-4 )   322 - 328   2010.12

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  • g-Cyclodextrins possessing an azido group and a triisopropylbenzenesulfonyl group as useful synthetic and authentic intermediates for unsymmetrically functionalized derivatives Reviewed

    Yoshihide Himeno, Atsushi Miyagawa, Masao Kawai, Hatsuo Yamamura

    Tetrahedron   65 ( 45 )   9474 - 9480   2009.11

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • gamma-Cyclodextrins possessing an azido group and a triisopropylbenzenesulfonyl group as useful synthetic and authentic intermediates for unsymmetrically functionalized derivatives Reviewed

    Yoshihide Himeno, Atsushi Miyagawa, Masao Kawai, Hatsuo Yamamura

    TETRAHEDRON   65 ( 45 )   9474 - 9480   2009.11

     More details

    Language:English   Publishing type:Research paper (scientific journal)   Publisher:PERGAMON-ELSEVIER SCIENCE LTD  

    Seven isomers of cyclomaltooctaose (gamma-cyclodextrin) whose C6s were unsymmetrically disubstituted with both an azido group and an arenesulfonyloxy group were prepared and each of them was isolated by reversed phase chromatography. The assignment of the modified positions in each regioisomers was unambiguously performed by chemical correlation with the authentic compounds and chemical conversion to the 3,6-anhydro derivatives followed by high-resolution 2D-(1)H NMR (COSY, TOCSY, and HO-HAHA) analyses. The compounds are versatile synthetic and authentic intermediates to prepare sophisticated derivatives with two different functionalities at desired positions on the molecule for supramolecular chemistry. (C) 2009 Elsevier Ltd. All rights reserved.

    DOI: 10.1016/j.tet.2009.08.061

    Web of Science

    researchmap

  • Development of Membrane Filter with Oligosaccharide Immobilized by Click Chemistry for Influenza Virus Adsorption Reviewed

    Tomohisa Kato, Atsushi Miyagawa, Maria Carmelita Z. Kasuya, Kenichi Hatanaka

    The Open Chemical and Biomedical Methods Journal   2   13 - 17   2009.04

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Elimination Filter for Verotoxins -Highly Adsorbing by Glycoconjugate Polymer- Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Chemistry Letters   37 ( 4 )   438 - 439   2008.03

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Purification by Centrifugal Partition Chromatography of amphiphilic compounds, glycolipids and pseudo-glycolipids synthesized by using cells Reviewed

    T. Kato, A. Miyagawa, MC. Kasuya, A. Ito, K. Hatanaka

    Journal of Chromatography A   1178 ( 1-2 )   154 - 159   2008.01

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Alternative methods of globotrioside production using Vero cells a microcarrier system procedure Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Chemistry Central Journal   1   26   2007.11

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Alternative methods of globotrioside production using Vero cells: a microcarrier system procedure Reviewed

    Atsushi Miyagawa, Maria Carmelita Z. Kasuya, Kenichi Hatanaka

    CHEMISTRY CENTRAL JOURNAL   1   26   2007.11

     More details

    Language:English   Publishing type:Research paper (scientific journal)   Publisher:BIOMED CENTRAL LTD  

    Background: Glycolipids are one component of cell membranes, and are found most prevalently at the surface of the plasma membrane. Animal cells take in amphipathic glycosides, which are later glycosylated after assimilation in biosynthetic pathways. Gycosylated glycosides are released outside of cells to the surrounding culture medium. This represents an accessible method of obtaining complex glycosides.
    Results: Vero cells are sensitive to Shiga toxins and are known to express the glycosides globotriaosyl ceramide (Gb3) and globotetraosyl ceramide (Gb4) on the surface of the plasma membrane. By administering amphipathic lactosides to Vero cells, the above mentioned glycolipids could be produced by the action of cellular enzymes. In our study, the optimum conditions (seeded cell number, incubated time period, 12-azidododecyl lactoside concentration and medium volume) for the production of Gb3 analogue were investigated. The 87.9 mu g/100 mm dish (11.7% yield) Gb3 analogue was produced under appropriate conditions. The large-scale culture of Vero cells using a microcarrier culture method with repetitions produced about 30 mg of the Gb3 analogue.
    Conclusion: The mass production of glycosides in Vero cells was carried out on a microcarrier with repeated administration of 12-azidododecyl lactoside. The results indicated that the use of both a microcarrier culture and repetition were highly effective in the production of Gb3, Gb4 and sialyl lactoside (GM3) type-oligosaccharides.

    DOI: 10.1186/1752-153X-1-26

    Web of Science

    researchmap

  • Inhibitory effects of glycopolymers having globotriose and/or lactose on cytotoxicity of Shiga toxin 1 Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Carbohydrate Polymers   67 ( 2 )   260 - 264   2007.01

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Applications of Immobilized Glycopolymers -Development and potentiality of the adsorption filter for influenza virus Reviewed

    A. Miyagawa, M. Nakane, K. Hatanaka

    seisan kenkyu   59 ( 2 )   110 - 113   2007.01

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • 糖鎖高分子の医療用途を考える

    宮川 淳、畑中 研一

    未来材料   6 ( 7 )   32 - 37   2006.07

     More details

    Language:Japanese   Publishing type:Research paper (other academic)  

  • Structural Analysis of the Interaction between Shiga Toxin B Subunits and Linear Polymers Bearing Clustered Globotriose Residues Reviewed

    M. Watanabe, K. Igai, K. Matsuoka, A. Miyagawa, T. Watanabe, R. Yanoshita, Y. Samejima, D. Terunuma, Y. Natori, K. Nishikawa

    Infection and Immunity   74 ( 3 )   1984 - 1988   2006.03

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Immobilization of Glycoconjugate Polymers on Cellulose Membrane for Affinity Separation Reviewed

    A. Miyagawa, MC. Kasuya, K. Hatanaka

    Bulletin of the Chemical Society of Japan   79 ( 2 )   348 - 356   2006.02

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Development of dialyzer with immobilized glycoconjugate polymers for removal of Shiga-toxin Reviewed

    A. Miyagawa, M. Watanabe, K. Igai, MC. Kasuya, Y. Natori, K. Nishikawa, K. Hatanaka

    Biomaterials   27 ( 17 )   3304 - 3311   2006.02

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Synthesis of polyesters from 5-hydroxymethyl-2-furfural as a starting material Reviewed

    K. Hatanaka, D. Yoshida, K. Okuyama, A. Miyagawa, K. Tamura, N. Sato, K. Hashimoto, M. Sagehashi, A. Sakoda

    Kobunshi Ronbunshu   62   316 - 320   2005.07

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Syntheses of polyesters from 5-hydroxymethyl-2-furfural as a starting material Reviewed

    K Hatanaka, D Yoshida, K Okuyama, A Miyagawa, K Tamura, N Sato, K Hashimoto, M Sagehashi, A Sakoda

    KOBUNSHI RONBUNSHU   62 ( 7 )   316 - 320   2005

     More details

    Language:Japanese   Publishing type:Research paper (scientific journal)   Publisher:SOC POLYMER SCIENCE JAPAN  

    Polyesters were synthesized from 5-hydroxymethyl-2-furfural (HMF), which can be prepared by pyrolysis of biomass or cellulose. 2,5-Bis (hydroxymethyl) furan (BHF), which was prepared by the reduction of HMF, and natural dicarboxylic acids such as succinic acid, fumaric acid, or maleic acid were polymerized to give polyesters. Polycondensations were carried out by two methods: one used acid chloride and the other one used a condensing reagent. Polycondensation of BHF and succinic acid gave a polymer of which the number averaged degree of polymerization was 30. NMR and IR spectra indicated that the obtained polymers have linear and regular polyesters. Copolymerization performed using the mixture of two kinds of dicarboxylic acids gave the copolymers. DSC measurements of polyesters showed the melting temperature and the grass transition temperature.

    Web of Science

    researchmap

  • Fluorous-tagged compound: a viable scaffold to prime oligosaccharide synthesis by cellular enzymes Reviewed

    MC. Kasuya, R. Cusi, O. Ishihara, A. Miyagawa, K. Hashimoto, T. Sato, K. Hatanaka

    Biochemical and Biophysical Research Communication   316 ( 3 )   599 - 604   2004.04

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Synthesis of glycoconjugate polymer carrying globotriaose as artificial multivalent ligand for Shigatoxin-producing Escherichia coli O157: H7. Reviewed

    A. Miyagawa, H. Kurosawa, T. Watanabe, T. Koyama, D. Terunuma, K. Matsuoka

    Carbohydrate Polymers   57   441 - 450   2004.03

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Development of Devoce Using Glyco-polymer for Treatment of Infection by Escherichia coli O157 Reviewed

    A. Miyagawa, K. Hatanaka

    seisan kenkyu   56 ( 3 )   227 - 231   2004.03

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

  • Oral therapeutic agents with highly clustered globotriose for treatment of Shiga toxigenic Escherichia coli infections Reviewed

    M. Watanabe, K. Matsuoka, E. Kita, K. Igai, N. Higashi, A. Miyagawa, T. Watanabe, R. Yanoshita, Y. Samejima, D. Terunuma, Y. Natori, K. Nishikawa

    The Journal of Infectious Diseases   189 ( 3 )   360 - 368   2004.02

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

To the head of this page.▲