{"id":46,"date":"2020-03-06T13:33:04","date_gmt":"2020-03-06T04:33:04","guid":{"rendered":"http:\/\/web.tohoku.ac.jp\/bp\/?page_id=46"},"modified":"2026-04-14T15:10:49","modified_gmt":"2026-04-14T06:10:49","slug":"publications","status":"publish","type":"page","link":"https:\/\/web.tohoku.ac.jp\/bp\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n

Abe K, Koizumi N, Takazaki H, Hirose M, Takabe K, Kato T, Nakamura S
A novel periplasmic layer formed by an outer membrane lipo-protein governs the cell-envelope integrity and stiffness of Leptospira interrogans<\/em>
Submitted, bioRxiv<\/a> (2026)<\/p>\n\n\n\n

Xu J, Nakamura S, Tomoyose S, Shimabuku R, Tomioka R, Yamashiro T
Light-activated cAMP signaling controls sodium-driven motility in Vibrio cholerae<\/em>
PNAS<\/a>, 123 (15) e2530860123 (2026) \u6771\u5317\u5927\u5b66\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/a><\/p>\n\n\n\n

Kawamoto A*, Kuribayashi T, Morita M, Nakamura S*, Koizumi N*
Asymmetric sheath coordination controls flagellar architecture and function in Leptospira<\/em> spirochete
EMBO J.<\/a> (2026) DOI: 10.1038\/s44318-026-00731-1 (*co-corresponding authors)
\u6771\u5317\u5927\u5b66\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/a><\/p>\n\n\n\n

Hou RZ, Toyabe S, Wang ZS
Recover a long-missing thermodynamic limit from experimental trajectories of F1-ATPase molecular motor
BBA – Bioenergetics<\/a> 1867, 149583 (2026).<\/p>\n\n\n\n

Ishihara T, Uchida N*, Nakamura S*
Emergent hydrodynamic synchronization between microbeads labeling bacterial flagellar motors
Submitted, bioRxiv<\/a> (2026) (*co-corresponding authors)<\/p>\n\n\n\n

Brock EE, Matthews SA, Cohen EJ, Nakamura S, Wilson LG
Species-specific surface dwell times and accumulation of microbes investigated by holographic microscopy
Phil. Trans. R. Soc. A., 383:20240265<\/a><\/p>\n\n\n\n

Aoyanagi H, Magi Y, Toyabe S
Experimental demonstration of kinetic proofreading inherited in ligation-based information replication
Phys. Rev. Res. <\/a>7, 043264 (2025)<\/p>\n\n\n\n

Oikawa S, Nakayama Y, Ito S, Sagawa T, Toyabe S
Experimentally achieving minimal dissipation via thermodynamically optimal transport
Nature Commun.<\/a> 16, 10424 (2025), Press release (in Japanese)<\/a><\/p>\n\n\n\n

Mishima T, Gupta D, Nakayama Y, Wareham WC, Ohyama T, Sivak DA*, Toyabe S*
Efficiently driving F1 molecular motor in experiment by suppressing nonequilibrium variation
Phys. Rev. Lett.<\/a> 135, 148402 (2025), featured in Physics<\/a>.
* co-corresponding authors<\/p>\n\n\n\n

Fukuda A, Nakayama Y, Toyabe S
Acceleration of enzymatic reaction-diffusion kinetics by intermediate state
Phys. Rev. E<\/a> 112, 034403 (2025)<\/p>\n\n\n\n

Nakayama Y and Toyabe S
Asymmetric enzyme kinetics of F1-ATPase induced by rotation-assisted substrate binding
Phys. Rev. Res.<\/em><\/a> 7, 023213 (2025)<\/p>\n\n\n\n

Xu J, Abe K, Kodama T, Sultana M, Chac D, Markiewicz SM, Matsunami H, Kuba E, Tsunoda S, Alam M, Weil AA, Nakamura S, Yamashiro T
The role of morphological adaptability in Vibrio cholerae\u2019s motility
mBio<\/a> in press<\/p>\n\n\n\n

Nakamura S, Minamino T
Structure and dynamics of the bacterial flagellar motor complex
Biomolecules<\/a> 14, 1488 (2024)<\/p>\n\n\n\n

Takahashi T, Aoyanagi H, Pigolotti S, Toyabe S
Blocking uncertain mispriming errors of PCR
Biophys. J<\/a> 123, 3558 – 3568 (2024)
GitHub site<\/a><\/p>\n\n\n\n

Kai T*, Abe T*, Yoshinaga N, Nakamura S, Kudo S, Toyabe S
Collective gradient sensing by dilute swimming bacteria without clustering
Phys. Rev. Res.<\/a> 6, L032061 (2024)
* equally contributed<\/p>\n\n\n\n

Patent Application
\u7279\u98582024-139284
\u767a\u660e\u8005\uff1a\u9ce5\u8c37\u90e8\u7965\u4e00\uff0c\u4e2d\u5c71\u6d0b\u5e73\uff0c\u53ca\u5ddd\u664b\u609f\uff0c\u6c99\u5ddd\u8cb4\u5927\uff0c\u4f0a\u85e4\u5275\u7950
\u8d70\u67fb\u30d1\u30bf\u30fc\u30f3\u60c5\u5831\u751f\u6210\u88c5\u7f6e\u3001\u8d70\u67fb\u30d1\u30bf\u30fc\u30f3\u60c5\u5831\u751f\u6210\u65b9\u6cd5\u3001\u8d70\u67fb\u30d1\u30bf\u30fc\u30f3\u60c5\u5831\u751f\u6210\u30d7\u30ed\u30b0\u30e9\u30e0\u3001\u53ca\u3073\u3001\u30ec\u30fc\u30b6\u5149\u7167\u5c04\u30b7\u30b9\u30c6\u30e0
\u51fa\u9858\u4eba\uff1a\u6771\u5317\u5927\u5b66\uff0c\u6771\u4eac\u5927\u5b66
\u51fa\u9858\u65e5\uff1a2024\u5e748\u670820\u65e5<\/p>\n\n\n\n

\u4e2d\u6751\u4fee\u4e00
\u7d30\u83cc\u306e\u63a5\u7740\u6027\u3068\u904b\u52d5\u6027\u306e\u610f\u7fa9\uff5e\u6a5f\u68b0\u5b66\u7fd2\u3067\u660e\u3089\u304b\u306b\u306a\u3063\u305f\u75c5\u539f\u6027\u3068\u306e\u95a2\u4fc2\uff5e
\u751f\u7269\u7269\u7406<\/a>, 64, 190-192 (2024)<\/p>\n\n\n\n

Strnad M, Koizumi N, Nakamura S, Vancov\u00e1 M, Rego R.O.M.
It\u2019s not all about flagella \u2013 sticky invasion by pathogenic spirochetes
Trends. Parasitol.<\/a>, 40, 378-385 (2024)<\/p>\n\n\n\n

Ito KI, Sato Y, Toyabe S
Design of artificial molecular motor inheriting directionality and scalability.
Biophys. J.<\/a> 123, 858-866 (2024)<\/p>\n\n\n\n

Abe K, Koizumi N, Nakamura S
Machine learning-based motion tracking reveals an inverse correlation between adhesivity and surface motility of the leptospirosis spirochete
Nat. Commun<\/a>., 14, 7703 (2023)\u3000\u6771\u5317\u5927\u5b66\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/a>\uff0cMIT Technology Review<\/a><\/p>\n\n\n\n

Aoyanagi H, Pigolotti S, Ono S, Toyabe S
Error-suppression mechanism of PCR by blocker strands
Biophys. J.<\/a> 122, 1334 – 1341 (2023)<\/p>\n\n\n\n

Gupta D, Large S J., Toyabe S, Sivak D A
Optimal control of the F1-ATPase molecular motor
J. Phys. Chem. Lett.<\/a> 13, 11844-11849 (2022)<\/p>\n\n\n\n

Toyabe S
Rotary Molecular motors
(contribution (section 5.4) to “Molecular Robotics: An Introduction<\/a>” edited by Satoshi Murata), Springer (2022) \"Amazon\"<\/a><\/p>\n\n\n\n

\u9ce5\u8c37\u90e8\u7965\u4e00\u8457 \u300e\u751f\u7269\u7269\u7406\u5b66<\/a>\u300f (2022)
\u65e5\u672c\u8a55\u8ad6\u793e \u7269\u7406\u5b66\u30a2\u30c9\u30d0\u30f3\u30b9\u30c8\u30b7\u30ea\u30fc\u30ba\uff08\u5927\u585a \u5b5d\u6cbb, \u4f50\u91ce \u96c5\u5df1, \u5bae\u4e0b\u7cbe\u4e8c \u7de8\u96c6\uff09 \"Amazon\"<\/a>
\u30b5\u30dd\u30fc\u30c8\u30b5\u30a4\u30c8\uff08Python\u7528\u30bd\u30fc\u30b9\u30b3\u30fc\u30c9\uff09\uff1a https:\/\/stoyabe.github.io\/biophys\/<\/a><\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

Xu J, Koizumi N, Morimoto YV, Ozuru R, Masuzawa T, Nakamura S
Light dependent synthesis of a nucleotide second messenger controls the motility of a spirochete bacterium
Sci Rep<\/a> (2022) 12, 6825 <\/p>\n\n\n\n

Nakamura S
Motility of the zoonotic spirochete Leptospira<\/em>: Insight into association with pathogenicity
Int. J. Mol. Sci.<\/a> (2022) 23, 1859<\/p>\n\n\n\n

Nakao R, Masuzawa T, Nakamura S, Koizumi N
Complete genome sequence of Leptospira kobayashii<\/em> strain E30, isolated from soil in Japan
Microbiol Resour Announc<\/a> (2021) 10, e0090721<\/p>\n\n\n\n

Kokubu E, Kikuchi Y, Okamoto\u2010Shibayama K, Nakamura S, Ishihara K
Crawling motility of Treponema denticola<\/em> modulated by outer sheath protein
Microbiol Immunol. <\/a>(2021) <\/p>\n\n\n\n

\u4e2d\u5c71\u6d0b\u5e73\uff0c\u9ce5\u8c37\u90e8\u7965\u4e00
\u5206\u5b50\u304c\u306f\u305f\u3089\u304f\u3068\u3044\u3046\u3053\u3068
\u73fe\u4ee3\u5316\u5b66 <\/a>605, 30 (2021) \uff082021\u5e748\u6708\u53f7\uff09<\/p>\n\n\n\n

Ito KI, Nakamura S, Toyabe S,
Cooperative stator assembly of bacterial flagellar motor mediated by rotation
Nature Communications<\/a> 12, 3218 (2021).<\/p>\n\n\n\n

Nakayama Y, Toyabe S
Optimal rectification without forward-current suppression by biological molecular motor.
Phys. Rev. Lett.<\/a> 126, 208101 (2021) (preprint: arXiv:2008.07106<\/a>)<\/p>\n\n\n\n

\u9ce5\u8c37\u90e8\u7965\u4e00
\u751f\u4f53\u5206\u5b50\u30e2\u30fc\u30bf\u30fc\u306e\u52d5\u4f5c\u30e1\u30ab\u30cb\u30ba\u30e0\u3068\u30a8\u30cd\u30eb\u30ae\u30fc\u8ad6.
Petrotech<\/a> 44, 421 (2021)<\/p>\n\n\n\n

Sebasti\u00e1n I, Okura N, Humbel BM, Xu J, Hermawan I, Matsuura C, Hall M, Takayama C, Yamashiro T, Nakamura S, Toma C
Disassembly of the apical junctional complex during the transmigration of Leptospira interrogans<\/em> across polarized renal proximal tubule epithelial cells.
Cell. Microbiol<\/a>. (2021) e13343<\/p>\n\n\n\n

Abe K, Kuribayashi T, Takabe K, Nakamura S.
Implications of back-and-forth motion and powerful propulsion for spirochetal invasion.
Sci. Rep.<\/a> (2020) 10, 13937 <\/p>\n\n\n\n

Xu J, Koizumi N, Nakamura S.
Crawling motility on the host tissue surfaces is associated with the pathogenicity of the zoonotic spirochete Leptospira<\/em>.
Front. Microbiol.<\/a> (2020) doi: 10.3389\/fmicb.2020.01886 <\/p>\n\n\n\n

\u9ce5\u8c37\u90e8\u7965\u4e00\uff0cBraun D.,
\u92f3\u578b\u8907\u88fd\u7cfb\u306b\u304a\u3051\u308b\u7a2e\u306e\u8d77\u6e90
\u751f\u7269\u7269\u7406 60, 295 – 299 (2020)<\/a><\/p>\n\n\n\n

Nakamura S
Measurement of the cell-body rotation of Leptospira<\/em>
Methods Mol Biol.<\/a> Leptospira<\/em> spp. 2134: 139-148. doi: 10.1007\/978-1-0716-0459-5_13 (2020) <\/p>\n\n\n\n

Toyabe S, Izumida Y.
Experimental characterization of autonomous heat engine based on minimal dynamical-system model.
Phys. Rev. Res<\/a> 2, 033146 (2020)<\/p>\n\n\n\n

Tanaka M, Kawakami T, Okaniwa T, Nakayama Y, Toyabe S, Ueno H, and Muneyuki E,
Tight chemomechanical coupling of the F1<\/sub> motor relies on structural stability
Biophys. J.<\/a> 119, 48 (2020) <\/p>\n\n\n\n

Morita T, Omori T, Nakayama Y, Toyabe S, and Ishikawa T,
Harnessing random low Reynolds number flow for net migration
Phys. Rev. E<\/a> 101, 063101 (2020)<\/p>\n\n\n\n

Li CB, Toyabe S,
Efficiencies of molecular motors: a comprehensible overview
Biophys. Rev.<\/a> 12, 419 – 423 (2020)<\/p>\n\n\n\n

Toyabe S, Li CB, Kinbara K,
Session 2SDA\u2014Nonequilibrium energetics of biological molecular machines
Biophys. Rev.<\/a> 12, 273 – 274 (2020)<\/p>\n\n\n\n

Nakamura S, Kage A
Session 3SCA – Diversity and universality of motile mechanism of living things: from intracellular dynamics to collective motion
Biophys Rev<\/a><\/em> 12: 293\u2013294 doi: org\/10.1007\/s12551-020-00629-0 (2020)<\/p>\n\n\n\n

Nakamura S
Spirochete flagella and motility (Review)
Biomolecules<\/a>. doi: 10.3390\/biom10040550 (2020) <\/p>\n\n\n\n

Miyata M, Robinson RC, Uyeda T.Q.P., et al.
Tree of motility \u2013 A proposed history of motility systems in the tree of life.
Genes Cells.<\/a> 25:6\u201321. (2020)<\/p>\n\n\n\n

Masuzawa T, Uno R, Matsuhashi N, Yamaguchi M, Xu J, Nakamura S
Comparison of Leptospira<\/em> species isolated from environmental water and soil in Japan.
Microbiol. Immun.<\/a> 63: 469-473 (2019)<\/p>\n\n\n\n

Nakamura S, Hanaizumi Y, Morimoto YV, Inoue Y, Erchard M, Minamino T, and Namba K
Direct observation of speed fluctuations of flagellar motor rotation at extremely low load close to zero
Mol. Microbiol.<\/a> (2019)<\/p>\n\n\n\n

Nakamura S, Minamino T.
Flagella-driven motility of bacteria. (Review)
Biomolecules<\/a>, 9: 279 (2019) <\/p>\n\n\n\n

\u4e2d\u6751\u4fee\u4e00\uff0e
\u7d30\u83cc\u306e\u904b\u52d5\u6a5f\u69cb\u306b\u95a2\u3059\u308b\u7814\u7a76 \u30fc\u5e73\u621031\u5e74\u9ed2\u5c4b\u5968\u5b66\u8cde\u53d7\u8cde\u8ad6\u6587\u30fc
\u65e5\u672c\u7d30\u83cc\u5b66\u96d1\u8a8c<\/a> 74: 157-165 (2019)<\/p>\n\n\n\n

Xu J, Koyanagi Y, Isogai E, Nakamura S.
Effects of fermentation products of the commensal bacterium Clostridium ramosum on motility, intracellular pH, and flagellar synthesis of enterohemorrhagic
Escherichia coli.
Arch. Microbiol. <\/a>201:841\u2013846  (2019) <\/p>\n\n\n\n

\u9ce5\u8c37\u90e8\u7965\u4e00\uff0e
\u56de\u8ee2\u5206\u5b50\u30e2\u30fc\u30bf\u30fc\uff0e
a chapter of “\u5206\u5b50\u30ed\u30dc\u30c6\u30a3\u30af\u30b9\u6982\u8ad6<\/a>” (CBI\u51fa\u7248, 2019) edited by Satoshi Murata<\/p>\n\n\n\n

Sato K, Nakamura S, Kudo S, Toyabe S,
Evaluation of the duty ratio of the bacterial flagellar motor by dynamic load control
Biophys. J<\/a>., 116, 1952 (2019)<\/p>\n\n\n\n

Toyabe S, Braun D
Cooperative ligation breaks sequence symmetry and stabilizes early molecular evolution
Phys. Rev. X<\/a> 9, 011056 (2019)  –  News in Nature Physics<\/a>,   ScienceDaily<\/a><\/p>\n\n\n\n

Suzuki Y, Morimoto YV, Oono K, Hayashi F, Oosawa K, Kudo S, Nakamura S (2019)
Effect of the MotA(M206I) mutation on torque generation and stator assembly in the Salmonella H+-driven flagellar motor.
J. Bacteriol.<\/a> 201:e00727-18. <\/p>\n\n\n\n

Okuno K, Xu J, Isogai E, Nakamura S (2019)
Salmonella Typhimurium is attracted to egg yolk and repelled by albumen.
Curr. Microbiol.<\/a> 76:393\u2013397. <\/p>\n\n\n\n

\u9ce5\u8c37\u90e8\u7965\u4e00\uff0e
\u751f\u4f53\u5206\u5b50\u30e2\u30fc\u30bf\u30fc\u3000\uff0d\u9032\u5316\u304c\u751f\u3093\u3060\u8d85\u9ad8\u6027\u80fd\u30ca\u30ce\u30de\u30b7\u30f3\u30fc\uff0e
\n\t\t\t\u7cbe\u5bc6\u5de5\u5b66\u4f1a\u8a8c<\/a> 84(11), 905 (2018)<\/p>\n\n\n\n

Tahara H, Takabe K, Sasaki Y, Kasuga K, Kawamoto A, Koizumi N, Nakamura S.
The mechanism of two-phase motility in the spirochete Leptospira: Swimming and crawling.
Sci. Adv.<\/a> 4, eaar7975 (2018)<\/p>\n\n\n\n

\u4e2d\u6751\u4fee\u4e00\uff0e
\u30b9\u30d4\u30ed\u30d8\u30fc\u30bf\u306e\u904b\u52d5\u30e1\u30ab\u30cb\u30ba\u30e0\uff0e
\u751f\u7269\u5de5\u5b66\u4f1a\u8a8c 96(4), p195-199\uff082018\uff09<\/p>\n\n\n\n

\u9ad8\u90e8\u97ff\u4ecb\uff0c\u5ddd\u672c\u6643\u5927\uff0c\u4e2d\u6751\u4fee\u4e00\uff0e
\u83cc\u4f53\u5185\u3079\u3093\u6bdb\u3092\u5229\u7528\u3059\u308b\u87ba\u65cb\u5f62\u7d30\u83cc\u306e\u904a\u6cf3\u30e1\u30ab\u30cb\u30ba\u30e0\uff0e
\u751f\u7269\u7269\u7406<\/a> 58\uff1a191-195\uff082018\uff09 <\/p>\n\n\n\n

Sasaki Y, Kawamoto A, Tahara H, Kasuga K, Sato R, Ohnishi M, Nakamura S, Koizumi N.
Leptospiral flagellar sheath protein FcpA interacts with FlaA2 and FlaB1 in Leptospira biflexa.
PLOS One<\/a> 13, e0194923 (2018)<\/p>\n\n\n\n

\u4e2d\u6751\u4fee\u4e00\uff0e
\n\t\t\t\u7d30\u83cc\u306e\u3079\u3093\u6bdb\u30e2\u30fc\u30bf\u30fc\uff1a\u52d5\u304d\u3092\u4e0e\u3048\u308b\u5206\u5b50\u30de\u30b7\u30f3\u306e\u4f5c\u52d5\u539f\u7406\uff0e
\n\t\t\tCSJ\u30ab\u30ec\u30f3\u30c8\u30ec\u30d3\u30e5\u30fc26\u300c\u5206\u5b50\u30de\u30b7\u30f3\u306e\u79d1\u5b66\u3000\u5206\u5b50\u306e\u52d5\u304d\u3068\u305d\u306e\u6a5f\u80fd\u3092\u898b\u308b\u300d\uff0cp91-96. \u5316\u5b66\u540c\u4eba\uff082017\uff09<\/p>\n\n\n\n

Takabe K, Kawamoto A, Tahara H, Kudo S, Nakamura S.
Implications of coordinated cell-body rotations for Leptospira motility.
Biochem. Biophys. Res. Commun.,<\/a> 491, p1040-1046 (2017) <\/p>\n\n\n\n

Terahara N, Noguchi Y, Nakamura S, Kami-ike N, Ito M, Namba K, Minamino T.
Load- and polysaccharide-dependent activation of the Na+-type MotPS stator in the Bacillus subtilis flagellar motor.
Sci. Rep.<\/a> 7: 46081 (2017) <\/p>\n\n\n\n

Takabe K, Tahara H, Md. Islam S, Affroze S, Kudo S, and Nakamura S.
Viscosity-dependent variations in the cell shape and swimming manner of Leptospira.
Microbiology<\/a> 163, p153-160 (2017)<\/p>\n\n\n\n

Nakamura S, Md. Islam S.
Motility of Spirochetes. Methods in Molecular Biology 1593 \u201cThe Bacterial Flagellum, Methods and Protocols\u201d, p243\u2013251. Springer (2017)<\/p>\n\n\n\n

S. Toyabe
\u751f\u547d\u73fe\u8c61\u306b\u304a\u3051\u308b\u975e\u5e73\u8861\u63fa\u3089\u304e\u3068\u305d\u306e\u5fdc\u7528
\n\t\t\t\u7269\u6027\u7814\u7a76<\/a> 6, 064211 (2017) (Lecture notes in Japanese)<\/p>\n\n\n\n

Sakamoto Y, Toyabe S
Assembly of a functional and responsive microstructure by heat bonding of DNA-grafted colloidal brick
Sci. Rep.<\/a> 7, 9104 (2017)<\/p>\n\n\n\n

Abe T, Nakamura S, Kudo S.
Bioconvection induced by bacterial chemotaxis in a capillary assay.
Biochem. Biophys. Res. Commun.<\/a> 483, p277-282 (2017)<\/p>\n\n\n\n

Toyabe S
Decoding Fluctuation: Diffusional Analysis of Biological Molecular Motors
J. Phys. Soc. Jpn. News Comments<\/a>, 13, 07 (2016) (News article) <\/p>\n\n\n\n

Affroze S, Md. Islam S, Takabe K, Kudo S, Nakamura S.
Characterization of leptospiral chemoreceptors using a microscopic agar drop assay.
Curr. Microbiol.<\/a> 73, 202-205. (2016)<\/p>\n\n\n\n

\n\t\t\tXu J, Nakamura S, Md. Islam S, Guo Y, Ihara K, Tomioka R, Masuda M, \n\t\t\tYoneyama H, Isogai E.
Mannose-binding lectin inhibits the motility of pathogenic \nSalmonella by affecting the driving forces of motility and the chemotactic \nresponse.
PLoS One \n\t\t\t<\/a>11, e0154165  (2016)<\/p>\n\n\n\n

Toyabe S., Sano M.
Nonequilibrium fluctuations in biological strands, machines, and cells (Review article).
J. Phys. Soc. Japan<\/a>, 84,  102001 (2015)<\/p>\n\n\n\n

Md. Shafiqul Islam, Yusuke V. Morimoto, Seishi Kudo, Shuichi Nakamura
H+ and Na+ are involved in flagellar rotation of the spirochete Leptospira
Biochem. Biophys. Res. Comm.<\/a>, 466, 196-200 (2015)<\/p>\n\n\n\n

Hayashi R., Sasaki K, Nakamura S., Kudo S., Inoue Y., Noji H. and Hayashi K..
Giant acceleration of diffusion observed in a single-molecule experiment on F1-ATPase.
Phys. Rev. Lett. 114, 248101 (2015)<\/p>\n\n\n\n

Nakamura S, Morimoto YV, Kudo S.
A lactose fermentation product produced by Lactococcus lactis subsp. lactis, acetate, inhibits the motility of flagellated pathogenic bacteria.
Microbiology 161, 701 (2015)<\/p>\n\n\n\n

Xu J, Guo Y, Nakamura S, Islam Md. S, Tomioka R, Yoneyama H, Isogai E.
Mannose-Binding Lectin Impairs Leptospira Activity through the Inhibitory Effect on the Motility of Cell.
Microbiological Research 171, 21 (2015)<\/p>\n\n\n\n

Guo Y, Fukuda T, Nakamura S, Bai L, Xu J, Kuroda K, Tomioka R, Yoneyama H, Isogai E.
Interaction between Leptospiral Lipopolysaccharide and Toll-like Receptor 2 in Pig Fibroblast Cell Line, and Inhibitory Effect of Antibody against Leptospiral Lipopolysaccharide on Interaction.
Asian Australas. J. Anim. Sci. 28: 273-279. (2015) <\/a><\/p>\n\n\n\n

Toyabe S. and Muneyuki E.
Single molecule thermodynamics of ATP synthesis by F1-ATPase
New J. Phys. 17: 015008 (2015) <\/a><\/p>\n\n\n\n

Nakamura S.,
\u30b9\u30d4\u30ed\u30d8\u30fc\u30bf\u306e\u5f62\u3068\u904b\u52d5
\u65e5\u672c\u7d30\u83cc\u5b66\u96d1\u8a8c 69: 527-538 (2014) <\/a><\/p>\n\n\n\n

Guo Y, Fukuda T, Donai K, Kuroda K, Masuda M, Nakamura S, Yoneyama H \n\t\t\tand Isogai E.
Leptospiral lipopolysaccharide stimulates the \n\t\t\texpression of toll-like receptor 2 and cytokines in pig fibroblasts.\n\t\t\t
Anim. Sci. J. in press. (2014) <\/p>\n\n\n\n

Islam Md. S, Takabe K, \n\t\t\tKudo S and Nakamura S.
Analysis of the chemotactic behaviour of \n\t\t\tLeptospira using microscopic agar-drop assay.
FEMS Microbiol. \n\t\t\tLett. 365: 39-44. (2014) <\/a><\/p>\n\n\n\n

Nakamura S, Minamino T, \n\t\t\tKami-ike N, Kudo S and Namba K.
Effect of the MotB(D33N) \n\t\t\tmutation on stator assembly and rotation of the proton-driven \n\t\t\tbacterial flagellar motor.
BIOPHYSICS 10: 35-41. (2014) \n\t\t\t<\/a><\/p>\n\n\n\n

Nakamura S., Leshansky A., Magariyama Y., Namba K., Kudo S..
Direct measurement of helical cell motion of the spirochete Leptospira.
Biophys. J. 106: 47-54. (2014)<\/a><\/p>\n\n\n\n

Che YS, Nakamura S, Morimoto YV, Kami-Ike N, Namba K, Minamino T.
Load-sensitive coupling of proton translocation and torque generation in the bacterial flagellar motor.
Mol. Microbiol. 91:175-184. (2014) <\/a><\/p>\n\n\n\n

Muneyuki E. and Toyabe S.
\u5206\u5b50\u30e2\u30fc\u30bf\u30fc\u306e\uff11\u5206\u5b50\u5b9f\u9a13\u71b1\u529b\u5b66
a chapter in “\uff11\u5206\u5b50\u30ca\u30ce\u30d0\u30a4\u30aa\u8a08\u6e2c” (\u5316\u5b66\u540c\u4eba) edited by Hiroyuki Noji (in Japanese)
see Amazon.co.jp<\/a><\/p>\n\n\n\n

Muneyuki E., Toyabe S., and Ueno H.
FoF1 \u30e2\u30fc\u30bf\u30fc
a book chapter in “\uff11\u5206\u5b50\u751f\u7269\u5b66” (\u5316\u5b66\u540c\u4eba) edited by Yoshie Harada and Shin-ichi Ishiwata (in Japanese) see Amazon.co.jp<\/a><\/p>\n\n\n\n

Castillo DJ, Nakamura S., YV. Morimoto, YS Che, N. Kami-ike, Kudo S., T. Minamino, K. Namba.
The C-terminal periplasmic domain of MotB is responsible for load-dependent control of the number of stators of the bacterial flagellar motor.
BIOPHYSICS<\/em> 9: 173-181. (2013) <\/a><\/p>\n\n\n\n

Kishikawa J, Ibuki T, Nakamura S, \n\t\t\tNakanishi A, Minamino T, Miyata T, Namba K, Konno H, Ueno H, Imada \n\t\t\tK, Yokoyama K.
Common evolutionary origin for the rotor domain of \n\t\t\trotary ATPases and flagellar protein export apparatus.
PLoS One. \n\t\t\t8:e64695. (2013)<\/a><\/p>\n\n\n\n

Takabe K, Nakamura S, Ashihara M, Kudo \n\t\t\tS.
Effect of osmolarity and viscosity on the motility of \n\t\t\tpathogenic and saprophytic Leptospira.
Microbiol. Immunol. \n\t\t\t57:236-9. (2013) <\/a><\/p>\n\n\n\n

Guo Y, Nakamura S, Ando T, Yoneyama H, Kudo S, and Isogai E.
The inhibition effect of antiserum on the motility of Leptospira.
Curr. Microbiol. 66:359-64. (2013) <\/a><\/p>\n\n\n\n

Morimoto Y.V., Nakamura S, Hiraoka K.D., Namba K, Minamino T.
Distinct roles of highly conserved charged residues at the MotA-FliG interface in bacterial flagellar motor rotation.
J. Bacteriol.195:474-81. (2013) <\/a><\/p>\n\n\n\n

Toyabe S. and Muneyuki E.
Experimental thermodynamics of single molecular motor
biophysics 9, 91 (2013) (Review article) <\/a><\/p>\n\n\n\n

Toyabe S. and \n\t\t\tMuneyuki E.
Information-to-free-energy conversion: utilizing \n\t\t\tthermal fluctuations
\n\t\t\tbiophysics 9, 107 (2013) (Review article) <\/a><\/p>\n\n\n\n

Muneyuki E. \n\t\t\tand Toyabe S.
Demonstration of Maxwell’s demon
a chapter in \n\t\t\t“\u30ca\u30ce\u30b9\u30b1\u30fc\u30eb\u30fb\u30df\u30af\u30ed\u30b9\u30b1\u30fc\u30eb\u304b\u3089\u898b\u3048\u308b\u30d3\u30c3\u30b0\u306a\u4e16\u754c” (Chuo University Press, 2013)\u3000 (in \n\t\t\tJapanese)
see amazon.co.jp<\/a><\/p>\n\n\n\n

Miyazaki S., Matsumoto M., Brier S. B., Higaki T., Yamada T., Okamoto T., Ueno H., Toyabe S., and Muneyuki E.
Properties of electrogenic activity of bacteriorhodopsin
Eur. Biophys. J. 42, 257 (2013) <\/a><\/p>\n\n\n\n

Kikuchi Y., Naka Y., Osakabe H., Okamoto T., Masaike T., Ueno H., Toyabe S., and Muneyuki E.
Thermodynamic analyses of nucleotide binding to an isolated monomeric \u03b2 subunit and the \u03b13\u03b23\u03b3 subcomplex of F1-ATPase
Biophys. J. 105, 2541 (2013) <\/a><\/p>\n\n\n\n

Toyabe S., Ueno H., and Muneyuki E.
Recovery of state-specific potential of molecular motor from single-molecule trajectory
EPL 97, 40004<\/a> (2012) <\/p>\n\n\n\n

Toyabe S. and Muneyuki E.
\u71b1\u3086\u3089\u304e\u3092\u5229\u7528\u3059\u308b\u2015\u60c5\u5831\u71b1\u6a5f\u95a2\u306e\u5b9f\u73fe\u2015
\u751f\u7269\u7269\u7406 52, 136 ( 2012)<\/a>  (Review article in Japanese) <\/p>\n\n\n\n

Faulds-Pain A., Birchall C., Aldridge C., Smith W.D., Grimaldi G.., Nakamura S., Miyata T., Gray J., Li G., Tang J.X., Namba K., Minamino T. and Aldridge P.D.
Flagellin redundancy in Caulobacter crescentus and its implications for flagellar filament assembly.
J. Bacteriol. 193, 2695-2707. (2011)<\/a><\/p>\n\n\n\n

Minamino T., Imada K., Kinoshita M., Nakamura S., Morimoto Y.V. and Namba K.
Structural insight into the rotational switching mechanism of the bacterial flagellar motor.
PLoS Biol. 9:e1000616. (2011) <\/a><\/p>\n\n\n\n

\u4e2d\u6751\u4fee\u4e00, \u5357\u91ce\u5fb9
\u6c34\u7d20\u30a4\u30aa\u30f3\u3067\u52d5\u304f\u7d30\u83cc\u3079\u3093\u6bdb\u30e2\u30fc\u30bf\u30fc\u306e\u69cb\u9020\u3068\u6a5f\u80fd
\u5316\u5b66\u3068\u751f\u7269, 49\u5dfb1\u53f7, 22-31 (2011) <\/a> (review in Japanese)<\/p>\n\n\n\n

Toyabe S., T. Watanabe-Nakayama, T. Okamoto, Kudo S., and Muneyuki E.
Thermodynamic efficiency and mechanochemical coupling of F1-ATPase
Proc. Natl. Acad. Sci. USA 108, 17951 (2011) <\/a><\/p>\n\n\n\n

Toyabe S.\n\t\t\t
\u60c5\u5831\u3068\u71b1\u3068\u60aa\u9b54\u2015\u71b1\u904b\u52d5\u3092\u5229\u7528\u3059\u308b
\u79d1\u5b66 \n\t\t\t81, 1142 (2011) <\/a> (Review article in Japanese) <\/p>\n\n\n\n

Toyabe S.
\u60c5\u5831\u3092\u81ea\u7531\u30a8\u30cd\u30eb\u30ae\u30fc\u306b\u5909\u63db\u3059\u308b
\u7269\u6027\u7814\u7a76 96, 11 (2011) <\/a>
– for a conference “Physics of Nonequilibrium Systems -Fluctuation and Collective Behavior-” at YITP (in Japanese) <\/p>\n\n\n\n

Fujii S., Kanaizuka K., Toyabe S., Kobayashi K., Muneyuki E., and Haga M.
Fabrication and Placement of a Ring Structure of Nanoparticles by a Laser-Induced Micronanobubble on a Gold Surface
Langmuir 27, 8605 (2011)<\/a><\/p>\n\n\n\n

Morimoto Y.V.*, Nakamura S.*, Kami-ike N., Namba K. and Minamino T. (*equal contribution)
Charged residues in the cytoplasmic loop of MotA are required for stator assembly in to the bacterial flagellar motor.
Mol. Microbiol. 78: 1117-1129. (2010)<\/a><\/p>\n\n\n\n

Nakamura S., Kami-ike N., Yokota J.P., Minamino, T. and K. Namba.
Evidence for symmetry in the elementary process of bidirectional torque generation by the bacterial flagellar motor.
Proc. Natl. Acad. Sci. USA. 107:17616-17620. (2010)<\/a><\/p>\n\n\n\n

Toyabe S., Sagawa \n\t\t\tT., Ueda M., Muneyuki E., and Sano M.
Experimental \n\t\t\tdemonstration of information-to-energy conversion and validation of \n\t\t\tthe generalized Jarzynski equality
Nature Physics 6, 988 (2010)<\/a> – see also News&Views<\/a>, Nature \n\t\t\tNews<\/a>, and YouTube<\/a><\/p>\n\n\n\n

Toyabe S., Okamoto T., Watanabe-Nakayama T., Taketani h., Kudo S., and Muneyuki E.
Nonequilibrium energetics of a single F1-ATPase molecule
Phys. Rev. Lett. 104, 198103 (2010)<\/a><\/p>\n\n\n\n

Toyabe S. and Muneyuki E.
Single-molecule nonequilibrium energetics of a \n\t\t\tmolecular-motor F1-ATPase
\u7269\u6027\u7814\u7a76 95, 320 \n\t\t\t(2010)<\/a>
– for a conference “4th Mini-symposium on Liquids” (in \n\t\t\tJapanese) <\/p>\n\n\n\n

Fujii S., Kobayashi K., Kanaizuka K., Okamoto T., Toyabe S., Muneyuki E., and Haga M.
Observation of DNA pinning at laser focal point on Au surface and its application to single DNA nanowire and cross-wire formation
Bioelectrochemistry 80, 26 (2010)<\/a><\/p>\n\n\n\n

Fujii S., Kobayashi K., Kanaizuka K., Okamoto T., Toyabe S., Muneyuki E., and Haga M.
Manipulation of Single DNA Using a Micronanobubble Formed by Local Laser Heating on a Au-coated Surface
Chem. Lett. 39, 92 (2010)<\/a><\/p>\n\n\n\n

Nakamura, S., Morimoto, Y.V., Kami-ike, N., Minamino, T., and K. Namba.
Role of conserved prolyl residue (Pro173) of MotA in the mechanochemical reaction cycle of the proton-driven flagellar motor of Salmonella.
J. Mol. Biol. 393:300-307. (2009) <\/a><\/p>\n\n\n\n

Nakamura S., Kami-ike N., Yokota J.P., Kudo S., Minamino T., and Namba K.
Effect of intracellular pH on the torque-speed relationship of bacterial proton-driven flagellar motor.
J. Mol. Biol. 386:332-338. (2008)<\/a><\/p>\n\n\n\n

Che Y-S., Nakamura S., Kojima S., \n\t\t\tKami-ike N., Namba K., and Minamino T.
Suppressor analysis of \n\t\t\tthe MotB(D33E) mutation to probe bacterial flagellar motor dynamics \n\t\t\tcoupled with proton translocation.
J. Bacteriol. 190:6660-6667. \n\t\t\t(2008)<\/a><\/p>\n\n\n\n

Toyabe S. and M. Sano
Evaluating Energy \n\t\t\tDissipation of a Brownian Particle in a Viscoelastic Fluid
Phys. \n\t\t\tRev. E 77, 041403 (2008)<\/a><\/p>\n\n\n\n

Watanabe-Nakayama T., Toyabe S., Kudo S., Sugiyama S., Yoshida M., and Muneyuki E.
Effect of external torque on the ATP-driven rotation of F1-ATPase
Biochem. Biophys. Res. Comm. 366, 951 (2008) <\/a><\/p>\n\n\n\n

Toyabe S., Jiang H. R., Nakamura T., Murayama Y., and Sano M.
Experimental Test of a New Equality: Measuring Heat Dissipation in an Optically Driven Colloidal System
Phys. Rev. E 75, 011122 (2007)<\/a><\/p>\n\n\n\n

T. Goto, S. Kudo and Y. Magariyama
Asymmetric Swimming Motion of Singly Flagellated Bacteria near a Rigid Surface.
a book chapter in Bio-mechanisms of Swimming and Flying, 3-15 (2007)<\/a><\/p>\n\n\n\n

\u897f\u9ce5\u7fbd\u6075\u7f8e\u3001\u66f2\u5c71\u5e78\u751f\u3001\u9ad8\u91ce\u6cf0\u6589\u3001\u98ef\u91ce\u6b63\u662d\u3001\u5de5\u85e4\u6210\u53f2
\u30ec\u30fc\u30b6\u30fc\u6697\u8996\u91ce\u9855\u5fae\u93e1\u3092\u7528\u3044\u305f\u30b5\u30eb\u30e2\u30cd\u30e9\u83cc\u3079\u3093\u6bdb\u306e\u3089\u305b\u3093\u30d1\u30e9\u30e1\u30fc\u30bf\u89b3\u6e2c.
\u53ef\u8996\u5316\u60c5\u5831\u5b66\u4f1a\u8ad6\u6587\u96c6,27(3), 15-21 (2007)<\/a><\/p>\n\n\n\n

Nakamura S., Adachi Y., Goto T. and Magariyama Y.
Improvement in motion efficiency of the spirochete Brachyspira pilosicoli in viscous environments.
Biophys. J. 90:3019\u20133026. (2006) <\/a><\/p>\n\n\n\n

Y. Hayashibara, T. Agui, T. Ito, M. Oohaba, E. Koyanagi, T. Sekine, M. Takeuchi, and S. Kudo
Educational program with making automatic machines continuously from the basic to the applications.
J. Robotics and Mechatronics,18, 215-221 (2006)<\/p>\n\n\n\n

Toyabe S. and Sano M.
Spatial Suppression of Error Catastrophe in a Growing Pattern
Physica D 203,1 (2005)<\/a><\/p>\n\n\n\n

Y. Takano, S. Kudo, M. Nishitoba, and Y. \n\t\t\tMagariyama
Analyses on Deformation of Helical Flagella of \n\t\t\tSalmonella.
JSME International J., C,48, 513-520 (2005) <\/p>\n\n\n\n

Y. Magariyama, M. Ichiba, K. Nakata, K. Baba, T. Ohtani, S. Kudo, T. Goto
Difference in bacterial motion between forward and backward swimming caused by the wall effect.
Biophys J. 88, 3648-3658 (2005)<\/p>\n\n\n\n

S. Kudo, N. Imai, M. Nishitoba, S. Sugiyama, and Y. Magariyama
Asymmetric swimming pattern of Vibrio alginolyticus cells with single-polar flagella.
FEMS Microbiol. Letters,242, 221-225 (2005)<\/p>\n\n\n\n

Y. Magariyama, S. Kudo, T. Goto and Y. Takano\n\t\t\t
An Engineering Perspective on Swimming Bacteria: High-Speed \n\t\t\tFlagellar Motor, Intelligent Flagellar Filaments, and Skillful \n\t\t\tSwimming in Viscous Environments
Bio-mechanisms of Swimming and \n\t\t\tFlying, 1-12 (2004)<\/p>\n\n\n\n

S. Sugiyama, Y. Magariyama and S. Kudo
Forced rotation of Na+-driven flagellar motor in a coupling-ion free environment.
Biochimica et Biophysica Acta,1656,32-36 (2004)<\/p>\n\n\n\n

Y. Takano, K. Yoshida, S. Kudo, M. Nishitoba and Y. Magariyama
Analysis of small deformation of Helical flagellum of swimming Vibrio alginolyticus.
JSME International J., C,46, 1241-1247 (2003)<\/p>\n\n\n\n

Y. Magariyama and S. Kudo
A Mathematical \n\t\t\tExplanation of an Increase in Bacterial Swimming Speed with \n\t\t\tViscosity in Linear-Polymer Solutions.
Biophys. J. 83,733-739 \n\t\t\t(2002)<\/p>\n\n\n\n

\u5ddd\u4e45\u4fdd\u9054\u4e4b\u3001\u5de5\u85e4\u6210\u53f2\u3001\u53e4\u91ce\u6cf0\u4e8c\u3001\u524d\u7530\u5fe0\u8a08
\u57fa\u790e\u3068\u3057\u3066\u306e\u7269\u7406\u5b66 (\u751f\u547d\u79d1\u5b66\u306e\u57fa\u790e\u30b7\u30ea\u30fc\u30ba\u7b2c2\u5dfb)
\n\t\t\t\u5b9f\u6559\u51fa\u7248 (2002)<\/p>\n\n\n\n

Y. Magariyama, S. Masuda, Y. Takano, T. Ohtani, and S. Kudo
Difference between forward and backward swimming speeds of the single-polar-flagellated bacterium, Vibrio alginolyticus.
FEMS Microbiol. Letters 205, 343-347 (2001)<\/p>\n\n\n\n

Y. Magariyama, S. Sugiyama and S. Kudo
Bacterial swimming speed and rotation rate of bundled flagella.
FEMS Microbiol. Letters,199,125-129 (2001)<\/p>\n\n\n\n

\u897f\u9ce5\u7fbd\u6075\u7f8e\u3001\u5de5\u85e4\u6210\u53f2
\u30d0\u30af\u30c6\u30ea\u30a2\u306e\u904b\u52d5\u3068\u3079\u3093\u6bdb\u30e2\u30fc\u30bf
\u65e5\u672c\u6a5f\u68b0\u5b66\u4f1a\u8a8c,104, 602-603 (2001)<\/p>\n\n\n\n

\u66f2\u5c71\u5e78\u751f\u3001\u5de5\u85e4\u6210\u53f2
\u30ca\u30ce\u30fb\u30de\u30a4\u30af\u30ed\u30de\u30b7\u30f3\u30b7\u30b9\u30c6\u30e0\u3068\u3057\u3066\u898b\u305f\u7d30\u83cc\u904b\u52d5
\u65e5\u672c\u6a5f\u68b0\u5b66\u4f1a\u8a8c,103, 38-41 (2000)<\/p>\n\n\n\n

\u9234\u6728\u4ec1\u3001\u76ca\u5b50\u4fe1\u90ce\u3001\u6749\u5c71\u6ecb\u3001\u5de5\u85e4\u6210\u53f2
\u751f\u4f53\u5206\u5b50\u6a5f\u69cb\u306b\u304a\u3051\u308b\u30c8\u30e9\u30a4\u30dc\u30ed\u30b8\u30fc\u73fe\u8c61\u306e\u89e3\u6790.
\u30c8\u30e9\u30a4\u30dc\u30ed\u30b8\u30b9\u30c8 44, 420-425 (1999)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2
\u5fae\u751f\u7269\u4e16\u754c\u306e\u904b\u52d5.
\u30d1\u30ea\u30c6\u30a3,13, 4-12<\/p>\n\n\n\n

S. \n\t\t\tKojima, T. Atsumi, K. Muramoto, S. Kudo, I. Kawagishi and M. Homma
\n\t\t\tVibrio alginolyticus mutants resistant to phenamil, a specific \n\t\t\tinhibitor of the sodium-driven flagellar motor.
J. Mol. Biol. \n\t\t\t265, 310-318 (1997)<\/p>\n\n\n\n

\u6749\u5c71\u6ecb\u3001\u5de5\u85e4\u6210\u53f2
\u3079\u3093\u6bdb\u30e2\u30fc\u30bf\u306e\u6a5f\u80fd\u89e3\u6790\u306b\u304a\u3051\u308b\u65b0\u5c55\u958b
\n\t\t\t\u5fdc\u7528\u7269\u7406\u5b66\u4f1a\u3001\u6709\u6a5f\u5206\u5b50\u30fb\u30d0\u30a4\u30aa\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u5206\u79d1\u4f1a\u30fb\u4f1a\u8a8c 8, 131-140 (1997) <\/p>\n\n\n\n

K. Muramoto, Y. Magariyama, M. Homma, I. Kawagishi, S. Sugiyama, Y. Imae and S. Kudo
Rotational fluctuation of the sodium-driven flagellar motor of Vibrio alginolyticus induced by binding of inhibitors
J. Mol. Biol. 259, 687-695 (1996)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2
\u30de\u30a4\u30af\u30ed\u4e16\u754c\u306e\u904b\u52d5\uff1a\u30d0\u30af\u30c6\u30ea\u30a2\u3068\u3079\u3093\u6bdb\u30e2\u30fc\u30bf.
\u65e5\u672c\u30ed\u30dc\u30c3\u30c8\u5b66\u4f1a\u8a8c,14, 1125-1128 (1996)<\/p>\n\n\n\n

\u83ca\u6c60\u4f51\u4e8c\u3001\u83ca\u6c60\u88d5\u5b50\u3001\u66f2\u5c71\u5e78\u751f\u3001\u6749\u5c71\u6ecb\u3001\u5de5\u85e4\u6210\u53f2
\u83cc\u8840\u75c7\u30e2\u30c7\u30eb\u306b\u304a\u3051\u308b\u767d\u8840\u7403\u30ec\u30aa\u30ed\u30b8\u30fc\u3000\u2014\u6bdb\u7d30\u8840\u7ba1\u30e2\u30c7\u30eb\u3092\u7528\u3044\u305f\u89b3\u5bdf\u2014.
Proc. 8th Jikei Symp. on Hemorheology, 53-60 (1996)<\/p>\n\n\n\n

Y. \n\t\t\tMagariyama, S. Sugiyama, K. Muramoto, I. Kawagishi, Y. Imae and S. \n\t\t\tKudo
Simultaneous Measurement of Bacterial Flagellar Rotation \n\t\t\tRate and Swimming Speed.
Biophys. J. 69, 2154-2162 (1995)<\/p>\n\n\n\n

K. Muramoto, I. Kawagishi, S. Kudo, Y. Magariyama, Y. Imae and M. Homma
High-speed Rotation and Speed Stability of the Sodium-driven Flagellar Motor in Vibrio alginolyticus
J. Mol. Biol. 251,50-58 (1995)<\/p>\n\n\n\n

Y. Kikuchi, Y. Magariyama, S. Sugiyama and S. Kudo
Leukocyte Rheology in a Model of Bacteria.
Microcirc. ann. 11, 31-32 (1995)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2\uff0c\u66f2\u5c71\u5e78\u751f\uff0c\u6749\u5c71\u6ecb
\u30d0\u30af\u30c6\u30ea\u30a2\u306e\u904b\u52d5\u3068\u3079\u3093\u6bdb\u30e2\u30fc\u30bf.
\u30c8\u30e9\u30a4\u30dc\u30ed\u30b8\u30b9\u30c8,40, 488-493 (1995)<\/p>\n\n\n\n

\u66f2\u5c71\u5e78\u751f\uff0c\u5de5\u85e4\u6210\u53f2
\u7d30\u83cc\u3079\u3093\u6bdb\u30e2\u30fc\u30bf\u306e\u6a5f\u80fd\u6e2c\u5b9a.
\u30e1\u30ab\u30e9\u30a4\u30d5 41, 38-39<\/p>\n\n\n\n

Very fast flagellar \n\t\t\trotation
Y. Magariyama, S. Sugiyama, K. Muramoto, Y. Maekawa, I. \n\t\t\tKawagishi, Y. Imae and S. Kudo
Nature 371, 752 (1994)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2\uff0c\u66f2\u5c71\u5e78\u751f\uff0c\u6749\u5c71\u6ecb
\u5206\u5b50\u6a5f\u68b0\u30fb\u3079\u3093\u6bdb\u30e2\u30fc\u30bf.
\u6a5f\u68b0\u306e\u7814\u7a76 46, 210-213 (1994)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2\u3001\u66f2\u5c71\u5e78\u751f\u3001\u6749\u5c71\u6ecb
\u751f\u7269\u306b\u5b66\u3076\u6280\u8853\u3092\u76ee\u6307\u3057\u3066\uff0d\u3079\u3093\u6bdb\u30e2\u30fc\u30bf\u306e\u7814\u7a76.
\u6280\u5831\u3000\u5b89\u5ddd\u96fb\u6a5f 58, 204-207 (1994)<\/p>\n\n\n\n

M. Washizu, Y. Kurahashi, H. Iochi, O. Kurosawa, S.-I. \n\t\t\tAizawa, S. Kudo, Y. Magariyama, and H .Hotani
Dielectrophoretic \n\t\t\tMeasurement of Bacterial Motor Characteristics.
IEEE Trans. \n\t\t\tIndustry Applicat. 29, 286-294 (1993)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2\uff0c\u66f2\u5c71\u5e78\u751f
\u7d30\u83cc\u3079\u3093\u6bdb\u30e2\u30fc\u30bf\u306e\u56de\u8ee2\u8a08\u6e2c.
\u6750\u6599\u79d1\u5b66,30, 210-214, (1993)<\/p>\n\n\n\n

N. Kami-ike, S. Kudo and H. Hotani
Rapid changes in flagellar rotation induced by external electric pulses.
Biophys. J.,60,1350-1355 (1991)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2\uff0c\u66f2\u5c71\u5e78\u751f\uff0c\u76f8\u6ca2\u614e\u4e00
\u30ec\u30fc\u30b6\u30fc\u6697\u8996\u91ce\u9855\u5fae\u93e1\u306b\u3088\u308b\u3079\u3093\u6bdb\u30e2\u30fc\u30bf\u306e\u56de\u8ee2\u8a08\u6e2c.
\u751f\u7269\u7269\u7406 31, 38-40 (1991)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2
\u751f\u7269\u306e\u5206\u5b50\u6a5f\u68b0
\u8c4a\u7530\u4e2d\u592e\u7814\u7a76\u6240 R&D \u30ec\u30d3\u30e5\u30fc 26, 31-47 (1991)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2
\u6975\u5fae\u306e\u56de\u8ee2\u6a5f\u68b0\uff1a\u3079\u3093\u6bdb\u30e2\u30fc\u30bf.
\u6771\u6d77\u5316\u5b66\u5de5\u696d\u4f1a\u5831 164, 1-4 (1991)<\/p>\n\n\n\n

S. Kudo, Y. Magariyama and S.-I. Aizawa
Abrupt changes in flagellar rotation observed by laser dark-field microscopy.
Nature 346, 677-680 (1990)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2, \u5c0f\u6fa4\u6b63\u90a6
\u8ad6 \u8907\u5408\u632f\u52d5\u5b50\u6cd5\u306b\u3088\u308b\u30bb\u30e9\u30df\u30c3\u30af\u30b9\u306e\u5f3e\u6027\u7387\u6e2c\u5b9a\uff08\u7b2c\uff11\u5831\uff09\uff0d\u7c21\u6613\u5316\u3068\u9ad8\u7cbe\u5ea6\u5316\uff0d.
\u65e5\u672c\u30bb\u30e9\u30df\u30c3\u30af\u30b9\u5354\u4f1a\u5b66\u8853\u8ad6\u6587\u8a8c,98, 653-657 (1990)<\/p>\n\n\n\n

\u5c0f\u6fa4\u6b63\u90a6, \u5de5\u85e4\u6210\u53f2
\u8907\u5408\u632f\u52d5\u5b50\u6cd5\u306b\u3088\u308b\u30bb\u30e9\u30df\u30c3\u30af\u30b9\u306e\u5f3e\u6027\u7387\u6e2c\u5b9a\uff08\u7b2c\uff12\u5831\uff09\uff0d\u9ad8\u6e29\u6e2c\u5b9a\uff0d.
\u65e5\u672c\u30bb\u30e9\u30df\u30c3\u30af\u5354\u4f1a\u5b66\u8853\u8ad6\u6587\u8a8c,98, 987-990 (1990)<\/p>\n\n\n\n

\u5c0f\u6fa4\u6b63\u90a6, \u5de5\u85e4\u6210\u53f2
\u8907\u5408\u632f\u52d5\u5b50\u6cd5\u306b\u3088\u308b\u30bb\u30e9\u30df\u30c3\u30af\u30b9\u306e\u5f3e\u6027\u7387\u6e2c\u5b9a.
\u30d5\u30a1\u30a4\u30f3\u30bb\u30e9\u30df\u30c3\u30af\u30b9,53, \n\t\t\t266-2741 (1990)<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2\uff0c\u5b9d\u8c37\u7d18\u4e00
\u30ec\u30fc\u30b6\u30fc\u659c\u5149\u6697\u8996\u91ce\u9855\u5fae\u93e1.
\u7d30\u80de,22, 267-270 (1990)<\/p>\n\n\n\n

H. Okino, M. Isomura, S. Yamaguchi, Y. Magariyama, S. Kudo and S.-I. Aizawa
Release of Flagellar Filament-Hook-Rod Complex by a Salmonella typhimurium Mutant Defective in the M-Ring of the Basal Body.
J. Bacteriol.,171(4), 2075-2082 (1989)<\/p>\n\n\n\n

S. Kudo and M. Ozawa
Evaluation and \n\t\t\tMinimization of Experimental Errors in Elastic Constants and \n\t\t\tInternal Friction Obtained by the Composite-Bar Method.
Jpn. J. \n\t\t\tAppl. Phys., 28 (Supplement 28-2),184-186 (1989)<\/p>\n\n\n\n

S. Kudo, J. Mizuno and H. Hasegawa
Raman Microprobe Study of Phase Transfor-mation in Y\uff12O\uff13-PSZ.
Adv. Ceramics,24,103-108 (1988)
<\/p>\n\n\n\n

\u5de5\u85e4\u6210\u53f2, \u6c34\u91ce\u4e8c\u90ce, \u9577\u8c37\u5ddd\u82f1\u96c4
Y\uff12O\uff13-PSZ \u306b\u304a\u3051\u308b\u5fdc\u529b\u8a98\u8d77\u76f8\u5909\u614b\u306e\u9855\u5fae\u30e9\u30de\u30f3\u89b3\u5bdf.
\u7aaf\u696d\u5354\u4f1a\u8a8c,94(8),(1986),737-741<\/p>\n\n\n\n

S. Kudo
X-Ray Determination of \n\t\t\tIncommensurate Superlattices in K\uff12SeO\uff14 and (NH\uff14)\uff12BeF\uff14.
Jpn. J. \n\t\t\tAppl. Phys.,21,255-258 (1982)<\/p>\n\n\n\n

S. Kudo and T. Ikeda
Birefringence and Lattice Strain in K\uff12SeO\uff14.
J. Phys. Soc. Jpn.,50, 3681-3687 (1981)<\/p>\n\n\n\n

S. Kudo and T. Ikeda
Hydrostatic Pressure Effect on the Dielectric Properties of K\uff12SeO\uff14.
J. Phys. Soc. Jpn.,50(3),(1981),733-734<\/p>\n\n\n\n

S. Kudo and T. Ikeda
Elastic Compliance Anomalies in K\uff12SeO\uff14.
Jpn. J. Appl. Phys.,19(1),(1980),L45-L48<\/p>\n\n\n\n

S. Kudo and T. Hikita
Brillouin \n\t\t\tScattering Study of Ferroelectric (NH\uff14)\uff12BeF\uff14.
J. Phys. Soc. \n\t\t\tJpn.,45(5),(1978),1775-1776\n\n\n<\/p>\n\n\n\n

<\/p>\n","protected":false},"excerpt":{"rendered":"

Abe K, Koizumi N, Takazaki H, Hirose M, Takabe K, Kato T, Nakamura SA novel periplasmic layer f […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-46","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/pages\/46","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/comments?post=46"}],"version-history":[{"count":138,"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/pages\/46\/revisions"}],"predecessor-version":[{"id":9345,"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/pages\/46\/revisions\/9345"}],"wp:attachment":[{"href":"https:\/\/web.tohoku.ac.jp\/bp\/wp-json\/wp\/v2\/media?parent=46"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}