{"id":23,"date":"2012-03-23T18:21:28","date_gmt":"2012-03-23T09:21:28","guid":{"rendered":"http:\/\/www.rib.okayama-u.ac.jp\/saka\/?page_id=23"},"modified":"2025-09-02T11:38:27","modified_gmt":"2025-09-02T02:38:27","slug":"list-of-publications","status":"publish","type":"page","link":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/list-of-publications\/","title":{"rendered":"List of Publications"},"content":{"rendered":"\n<p><strong>2025<\/strong><\/p>\n\n\n\n<p>Sakamoto, W. Thylakostasis: Key Factors in Thylakoid Membrane Organization with Emphasis on Biogenesis and Remodeling Proteins in Vascular Plants. Plant &amp; cell physiology, pcaf098 Doi.org\/10.1093\/pcp\/pcaf098 (2025. 8.)<\/p>\n\n\n\n<p>Gachie, S.W., Muhire, A., Li, D., Kawamoto, A., Takeda-Kamiya, N., Goto, Y., Sato, M., Toyooka, K., Yoshimura, R., Takami, T., Zhang, L., Kurisu, G., Terachi, T., Sakamoto, W.<br>The thylakoid membrane remodeling protein VIPP1 forms bundled oligomers in tobacco chloroplasts. Plant physiology, 198(1):10.1093\/plphys\/kiaf137 Doi.org\/10.1093\/plphys\/kiaf137 (2025. 4. )<\/p>\n\n\n\n<p><strong>2024<\/strong><\/p>\n\n\n\n<p>Brunje A, Fussl M, Eirich J, Boyer J, Heinkow P, Neumann U, Konert M, Ivanauskaite A, Seidel J, Ozawa S, Sakamoto W, Meinnel T, Schwarzer D, Mulo P, Giglione C, Finkemeier I. The plastidial protein acetyltransferase GNAT1 forms a complex with GNAT2, yet their interaction is dispensable for state transitions. Mol. Cell Proteomics. 23: 100850. doi.org\/10.1016\/j.mcpro.2024.100850 (2024. 11.)<\/p>\n\n\n\n<p>\u52a0\u85e4\u88d5\u4ecb\u30fb\u5742\u672c \u4e98 \u5149\u5408\u6210\u53cd\u5fdc\u306b\u304a\u3051\u308b\u5149\u640d\u50b7\u3068\u4fee\u5fa9\u306e\u30e1\u30ab\u30cb\u30ba\u30e0\u306e\u89e3\u660e . \u5149\u30a2\u30e9\u30a4\u30a2\u30f3\u30b9 35: 9-12. (2024.9.)<\/p>\n\n\n\n<p>Matsushima R, Hisano H, Kim J.S, McNelly R, Oitome N.F, Seung D, Fujita N, Sato, K. Mutations in starch BRANCHING ENZYME 2a suppress the traits caused by the loss of ISOAMYLASE1 in barley. Theor. Appl. Genet. 137: 212. doi.org\/10.1007\/s00122-024-04725-7 (2024. 8.)<\/p>\n\n\n\n<p>Islam M.F, Yamatani H, Takami T, Kusaba M, Sakamoto W. Characterization of organelle DNA degradation mediated by DPD1 exonuclease in the rice genome-edited line. Plant Mol. Biol. 114: 71. doi.org\/10.1007\/s11103-024-01452-x (2024. 6.)<\/p>\n\n\n\n<p>Kumari P, Matsushima R, Hirayama T, Mikami K. Responses of the marine filamentous red alga \u02bbBangia\u02bc sp. ESS1 to recurrent changes in seawater concentration. Algal Res. 80: 103551. doi.org\/10.1016\/j.algal.2024.103551 (2024. 5.)<\/p>\n\n\n\n<p>Sakamoto W, Takami T. Plastid Inheritance Revisited: Emerging Role of Organelle DNA Degradation in Angiosperms. Plant Cell Physiol. 65: 484-492. doi.org\/10.1093\/pcp\/pcad104 (2024. 4.)<\/p>\n\n\n\n<p>Ozawa S.I, Zhang G, Sakamoto W. Dysfunction of Chloroplast Protease Activity Mitigates pgr5 Phenotype in the Green Algae Chlamydomonas reinhardtii. Plants (Basel) 13: 606. doi.org\/10.3390\/plants13050606 (2024. 2.)<\/p>\n\n\n\n<p><strong>2023<\/strong><\/p>\n\n\n\n<p>Sakamoto, W., Takami, T. Plastid inheritance revisited: emerging role of organelle DNA degradation in angiosperms. Plant Cell Physiol. doi.org\/10.1093\/pcp\/pcad104 (2023. 9. Online preview)<\/p>\n\n\n\n<p>Kato, Y., Kuroda, H., Ozawa, S. I., Saito, K., Dogra, V., Scholz, M., Zhang, G., de Vitry, C., Ishikita, H., Kim, C., Hippler,<br>M., Takahashi, Y., Sakamoto, W. Characterization of tryptophan oxidation affecting D1 degradation by FtsH in the photosystem II quality control of chloroplasts. Elife 12: RP88822. doi.org\/10.7554\/eLife.88822 (2023. 11.)<\/p>\n\n\n\n<p>Okegawa, Y., Sato, N., Nakakura, R., Murai, R., Sakamoto, W., Motohashi, K. x- and y-type thioredoxins maintain redox homeostasis on photosystem I acceptor side under fluctuating light. Plant Physiol. 193: 2498-2512. doi.org\/10.1093\/ plphys\/kiad466 (2023. 11.)<\/p>\n\n\n\n<p>Okegawa, Y. PCP Research Highlights: Regulator y Role of Three Important Post-Translational Modifications in Chloroplast Proteins. Plant Cell Physiol. 64: 1119-1123. doi.org\/10.1093\/pcp\/pcad097 (2023. 10.)<\/p>\n\n\n\n<p>Ogawa, Y., Iwano, M., Shikanai, T., Sakamoto, W. FZL, a dynamin-like protein localized to curved grana edges, is required for efficient photosynthetic electron transfer in Arabidopsis. Front. Plant Sci. 14: 1279699. doi.org\/10.3389\/fpls.2023.1279699 (2023. 9.)<\/p>\n\n\n\n<p>Sakamoto, W. Greetings from the PCP Editor-in-Chief. Plant Cell Physiol. 64: 701-703. doi.org\/10.1093\/pcp\/pcad061(2023. 7.)<\/p>\n\n\n\n<p>Sakamoto, W., Takami, T. Maternal plastid inheritance: two abating factors identified. Trends. Genet. 39: 342-343. doi.org\/ 10.1016\/j.tig.2023.03.002 (2023. 5.)<\/p>\n\n\n\n<p>Matsushima, R., Hisano, H., Galis, I., Miura, S., Crofts, N., Takenaka, Y., Oitome, N. F., Ishimizu, T., Fujita, N., Sato, K. FLOURY ENDOSPERM 6 mutations enhance the sugary phenotype caused by the loss of ISOAMYLASE1 in barley. Theor. Appl. Genet. 136: 94. doi.org\/10.1007\/s00122-023-04339-5 (2023. 4.)<\/p>\n\n\n\n<p><strong>2022<\/strong><\/p>\n\n\n\n<p>Osinde, C., Sakamoto, W., Kajiya-Kanegae, H., Sobhy, I. S., Tugume, A. K., Nsubuga, A. M., Galis, I. Identification of quantitative trait loci associated with sorghum susceptibility to Asian stem borer damage. J. Plant Interact. 18: 2153182. doi.org\/10.1080\/17429145.2022.2153182 (2022. 12.)<\/p>\n\n\n\n<p>\u5c0f\u5ddd \u7531\u30fb\u5742\u672c \u4e98 \u30c1\u30e9\u30b3\u30a4\u30c9\u819c\u306e\u5f62\u6210\u3068\u69cb\u9020\u7dad\u6301\u306b\u95a2\u4e0e\u3059\u308b\u819c\u30ea\u30e2\u30c7\u30ea\u30f3\u30b0\u5206\u5b50\uff0e \u5149\u5408\u6210\u7814\u7a76 32: 64-74. (2022. 8.)<\/p>\n\n\n\n<p>Okegawa, Y., Sakamoto, W., Motohashi, K. Functional division of f-type and m-type thioredoxins to regulate the Calvin cycle and cyclic electron transport around photosystem I. J. Plant Res. 135: 543-553. doi.org\/10.1007\/s10265-022- 01388-7 (2022. 7.)<\/p>\n\n\n\n<p>Takanashi, H., Kajiya-Kanegae, H., Nishimura, A., Yamada, J., Ishimori, M., Kobayashi, M., Yano, K., Iwata, H., Tsutsumi,<br>N., Sakamoto, W. DOMINANT AWN INHIBITOR Encodes the ALOG Protein Originating from Gene Duplication and Inhibits AWN Elongation by Suppressing Cell Proliferation and Elongation in Sorghum. Plant Cell Physiol. 63: 901-918. doi.org\/10.1093\/pcp\/pcac057 (2022. 7.)<\/p>\n\n\n\n<p>Ohnishi, N., Sugimoto, M., Kondo, H., Shioya, K. I., Zhang, L., Sakamoto, W. Distinctive in vitro ATP Hydrolysis Activity of AtVIPP1, a Chloroplastic ESCRT-III Superfamily Protein in Arabidopsis. Front. Plant Sci. 13: 949578. doi.org\/10.3389\/fpls.2022.949578 (2022. 7.)<\/p>\n\n\n\n<p>Ida, T., Crofts, N., Miura, S., Matsushima, R., Fujita, N. Starch Biosynthetic Protein Complex Formation in Rice ss2a be2b (+) Double Mutant Differs from Their Parental Single Mutants. J. Appl. Glycosci. 69: 23-33. doi.org\/10.5458\/jag.jag. JAG-2021_0015 (2022. 5.)<\/p>\n\n\n\n<p>Wahinya, F. W., Yamazaki, K., Jing, Z., Takami, T., Kamiya, T., Kajiya-Kanegae, H., Takanashi, H., Iwata, H., Tsutsumi, N., Fujiwara, T., Sakamoto, W. Sorghum Ionomics Reveals the Functional SbHMA3a Allele that Limits Excess Cadmium Accumulation in Grains. Plant Cell Physiol. 63: 713-728. doi.org\/10.1093\/pcp\/pcac035 (2022. 5.)<\/p>\n\n\n\n<p>Yamatani, H., Ito, T., Nishimura, K., Yamada, T., Sakamoto, W., Kusaba, M. Genetic analysis of chlorophyll synthesis and degradation regulated by BALANCE of CHLOROPHYLL METABOLISM. Plant Physiol. 189: 419-432. doi.org\/10.1093\/plphys\/kiac059 (2022. 5.)<\/p>\n\n\n\n<p>Nagamatsu, S., Wada, T., Matsushima, R., Fujita, N., Miura, S., Crofts, N., Hosaka, Y., Yamaguchi, O., Kumamaru, T. Mutation in BEIIb mitigates the negative effect of the mutation in ISA1 on grain filling and amyloplast formation in rice. Plant Mol. Biol. 108: 497-512. doi.org\/10.1007\/s11103-022-01242-3 (2022. 3.)<\/p>\n\n\n\n<p>Okegawa, Y., Tsuda, N., Sakamoto, W., Motohashi, K. Maintaining the Chloroplast Redox Balance through the PGR5-Dependent Pathway and the Trx System Is Required for Light-Dependent Activation of Photosynthetic Reactions. Plant Cell Physiol. 63: 92-103. doi.org\/10.1093\/pcp\/pcab148 (2022. 1.)<\/p>\n\n\n\n<p><strong>2021<\/strong><\/p>\n\n\n\n<p>Okegawa, Y., Tsuda, N., Sakamoto, W. and Motohashi, K. Maintaining the Chloroplast Redox Balance Through the PGR5-Dependent Pathway and the Trx System is Required for Light-Dependent Activation of Photosynthetic Reactions. Plant Cell Physiol. doi: 10.1093\/pcp\/pcab148. (2021. 10. Online preview)<\/p>\n\n\n\n<p>\u6876\u5ddd\u53cb\u5b63 \u30b7\u30ed\u30a4\u30cc\u30ca\u30ba\u30ca\u306b\u304a\u3044\u3066\u5149\u5316\u5b66\u7cfb I \u30b5\u30a4\u30af\u30ea\u30c3\u30af\u96fb\u5b50\u4f1d\u9054\u306f\u53b3\u5bc6\u306b\u5236\u5fa1\u3055\u308c\u3066\u3044\u308b. \u5149\u5408\u6210\u7814\u7a76 31 (3):154-161. (2021. 12.)<\/p>\n\n\n\n<p>\u5742\u672c \u4e98 \u5149\u5408\u6210\u88c5\u7f6e\u306e\u30a2\u30c3\u30bb\u30f3\u30d6\u30ea\u3068\u5206\u89e3\u306b\u3088\u308b\u30c0\u30a4\u30ca\u30df\u30af\u30b9. \u5149\u5408\u6210 pp.189-193.\uff08\u65e5\u672c\u5149\u5408\u6210\u5b66\u4f1a\u7de8\uff09ISBN 9784254171761 (2021. 12.)<\/p>\n\n\n\n<p>Jing, Z., Wacera, F. W., Takami, T., Takanashi, H., Fukada, F., Kawano, Y., Kajiya-Kanegae, H., Iwata, H., Tsutsumi, N. and Sakamoto, W. NB-LRR-encoding genes conferring susceptibility to organophosphate pesticides in sorghum. Sci. Rep.<br>11 (1): 19828. (2021. 10.)<\/p>\n\n\n\n<p>Taketa, S., Hattori, M., Takami, T., Himi, E. and Sakamoto, W. Mutations in a Golden2-Like Gene Cause Reduced Seed Weight in Barley albino lemma 1 Mutants. Plant Cell Physiol. 62 (3): 447-457. (2021. 7.)<\/p>\n\n\n\n<p>Gupta, T. K., Klumpe, S., Gries, K., Heinz, S., Wietrzynski, W., Ohnishi, N., Niemeyer, J., Spaniol, B., Schaffer, M., Rast, A., Ostermeier, M., Strauss, M., Plitzko, J. M., Baumeister, W., Rudack, T., Sakamoto, W., Nickelsen, J., Schuller, J. M., Schroda, M. and Engel, B. D. Structural basis for VIPP1 oligomerization and maintenance of thylakoid membrane<br>integrity. Cell 184 (14): 3643-3659. (2021. 7.)<\/p>\n\n\n\n<p>Sakamoto, W. Editorial Feature: Meet the PCP Editor-In-Chief-Wataru Sakamoto. Plant Cell Physiol. 62 (2): 222-223. (2021. 5.)<\/p>\n\n\n\n<p>Sakamoto, W. With Greetings and Hope for a Recoverable 2021: From the PCP Editor-In-Chief. Plant Cell Physiol. 62 (2): 219-221. (2021. 5.)<\/p>\n\n\n\n<p>Ida, T., Crofts, N., Miura, S., Matsushima, R. and Fujita, N. Structure and Properties of Starch in Rice Double Mutants Lacking Starch Synthase (SS) IIa and Starch Branching Enzyme (BE) Iib. J. Appl. Glycosci. 68: 31-39. (2021. 4.)<\/p>\n\n\n\n<p>Takanashi, H., Shichijo, M., Sakamoto, L., Kajiya-Kanegae, H., Iwata, H., Sakamoto, W. and Tsutsumi, N. Genetic dissection of QTLs associated with spikelet-related traits and grain size in sorghum. Sci. Rep. 11 (1): 9398. (2021. 4.)<\/p>\n\n\n\n<p>Nishioka, K., Kato, Y., Ozawa, S. I., Takahashi, Y. and Sakamoto, W. Phos-tag-based approach to study protein phosphorylation in the thylakoid membrane. Photosynth. Res. 147 (1): 107-124. (2021. 1.)<\/p>\n\n\n\n<p><strong>2020<\/strong><\/p>\n\n\n\n<p>Kajiya-Kanegae, H., Takanashi, H., Fujimoto, M., Ishimori, M., Ohnishi, N., Wacera, F. W., Omollo, E. A., Kobayashi, M., Yano, K., Nakano, M., Kozuka, T., Kusaba, M., Iwata, H., Tsutsumi, N and Sakamoto, W. (2020. 7. ) RAD-seq-Based High-Density Linkage Map Construction and QTL Mapping of Biomass-Related Traits in Sorghum using the Japanese Landrace Takakibi NOG. Plant Cell Physiol. 61: 1262-1272.<\/p>\n\n\n\n<p>Gupta, T. K., Klumpe, S., Gries, K., Heinz, S., Wietrzynski, W., Ohnishi, N.,Niemeyer, J., Schaffer, M., Rast, A., Strauss, M., Plitzko, J. M., Baumeister, W., Rudack, T., Sakamoto, W., Nickelsen, J., Schuller, J. M., Schroda, M. and Engel, B. D. (2020. 8. Online preview) Structural basis for VIPP1 oligomerization and maintenance of thylakoid membrane integrity. bioRxiv. doi: https:\/\/doi.org\/10.1101\/2020.08.11.243204<\/p>\n\n\n\n<p>Islam, M. S., Nguyen, T. V., Sakamoto, W. and Takagi, S. (2020. 9.) Phototropin- and photosynthesis-dependent mitochondrial positioning in Arabidopsis thaliana mesophyll cells. J Integr Plant Biol. 62:1352-1371.<\/p>\n\n\n\n<p><strong>2019<\/strong><\/p>\n\n\n\n<p>Ohnishi N, Wacera F, Sakamoto W (2019) Photosynthetic Responses to High Temperature and Strong Light Suggest Potential Post-flowering Drought Tolerance of Sorghum Japanese Landrace Takakibi. Plant Cell Physiol. <span class=\"cit\">1;60(9):2086-2099.<\/span><\/p>\n\n\n\n<p>\u5742\u672c\u3000\u4e98\u3001\u9ad8\u898b\u5e38\u660e (2019) \u30aa\u30eb\u30ac\u30cd\u30e9DNA\u3092\u81ea\u5df1\u5206\u89e3\u3057\u3066\u6804\u990a\u5206\u306b\u3059\u308b\u301c\u7d30\u80de\u5185\u5171\u751f\u304b\u3089\u751f\u3058\u305f\u7a2e\u5b50\u690d\u7269\u306e\u751f\u5b58\u6226\u7565\u301c. \u5316\u5b66\u3068\u751f\u7269 8\u6708\u53f7<\/p>\n\n\n\n<p>Duan J, Lee KP, Dogra V, Zhang S, Liu K, Caceres-Moreno C, Lv S, Xing W, Kato Y, Sakamoto W, Liu R, Macho AP, Kim C. (2019) Impaired PSII proteostasis promotes retrograde signaling via salicylic acid. Plant Physiol. <span class=\"cit\">180(4):2182-2197.<\/span><\/p>\n\n\n\n<p>Toyoshima, M., Sakata, M., Ohnishi, K., Tokumaru, Y., Kato, Y., Tokutsu, R., Sakamoto, W., Minagawa, J., Matsuda, F., Shimizu, H. (2019) Targeted proteome analysis of microalgae under high-light conditions by optimized protein extraction of photosynthetic organisms. J. Biosci. Bioeng. 127:394-402.<\/p>\n\n\n\n<p><strong>2018<\/strong><\/p>\n\n\n\n<p>Takami, T., Ohnishi, N., Kurita, Y., Iwamura, S., Ohnishi, M., Kusaba, M., Mimura, T., Sakamoto, W. (2018) Organelle DNA degradation contributes to the efficient use of phosphate in seed plants. Nat Plants. 4:1044-1055.<\/p>\n\n\n\n<p>Kato, Y., Hyodo, K., Sakamoto, W. (2018)The Photosystem II Repair Cycle Requires FtsH Turnover through the EngA GTPase. Plant Physiol. 178:596-611.<\/p>\n\n\n\n<p>Tanaka, M., Iamshchikov, I., Kato, Y., Sabirov, R., Gusev, O., Sakamoto, W. and Sugimoto, M (2018). Structure and molecular characterization of diadenosine polyphosphate hydrolase in brachypodium distachyon. J. Plant Biochem. Physiol. 6: 220.<\/p>\n\n\n\n<p>Tominaga, J., Nakahara, Y., Horikawa, D., Tanaka, A., Kamei, Y., Takami, T., Sakamoto, W., Unno, K., Sakamoto, A., and Shimada H. (2018) Overexpression of the protein disulfide isomaerase AtCYO1 in chloroplasts slows dark-induced senescence in Arabidopsis. BMC Plant Biol., 18:80.<\/p>\n\n\n\n<p>Kato, Y. and Sakamoto, W. (2018) FtsH protease in the thylakoid membrane: physiological functions and the regulation of protease activity. Frontiers Plant Sci., 9: 855. doi: 10.3389\/fpls.2018.00855.<\/p>\n\n\n\n<p>Nakamura, S., Hidema, J., Sakamoto, W., Ishida, H., and Izumi, M. (2018) Selective elimination of membrane-damaged chloroplasts via microautophagy. Plant Physiol., 177: 1007-1026.<\/p>\n\n\n\n<p>Sakamoto, W. and Takami T. (2018) Chloroplast DNA dynamics: copy number, quality control, and degradation. Plant Cell Physiol., 59: 1120-1127.<\/p>\n\n\n\n<p>Nishimura, K., Matsushita T., Shikanai, T., and Sakamoto, W. (2018) Meeting Report \u2013 Taiwan -Japan Plant Biology 2017, Spotlight Issue: From light signals\/signaling to photosynthesis and chloroplast development. Plant Cell Physiol., 59: 1099-1103.<\/p>\n\n\n\n<p>Ohnishi, N., Zhang, L., and Sakamoto, W. (2018) VIPP1 involved in chloroplast membrane integrity has GTPase activity in vitro. Plant Physiol. 177: 328-338.<\/p>\n\n\n\n<p>Szymanski, D., Bassham, D., Munnik, T., and Sakamoto, W. (2018) Cellular Dynamics: Cellular systems in the time domain. Plant Physiol. 176: 12-15.<\/p>\n\n\n\n<p>Yamatani, H., Kohzuma, K, Nakano, M., Takami, T., Kato, Y., Hayashi, Y., Monden, Y., Okumoto, Y., Abe, T., Kumamaru, T., Tanaka, A., Sakamoto, W., and Kusaba, M. (2018) Impairment of Lhca4, a subunit of LHCI, causes high accumulation of chlorophyll and the stay-green phenotype in rice. J. Exp. Bot., 69: 1027-1035.<\/p>\n\n\n\n<p><strong>2017<\/strong><\/p>\n\n\n\n<p>Salesse, C., Sharwood, R., Sakamoto, W., and Stern D. (2017) The rubisco chaperone BSD2 may regulate chloroplast coverage in maize bundle sheath cells. Plant Physiol. 175: 1624-1633.<\/p>\n\n\n\n<p>Kohzuma K, Sato Y, Ito H, Okuzaki A, Watanabe M, Kobayashi H, Nakano M, Yamatani H, Masuda Y, Nagashima Y, Fukuoka H, Yamada T, Kanazawa A, Kitamura K, Tabei Y, Ikeuchi M, Sakamoto W, Tanaka A, Kusaba M.(2017)&nbsp;The Non-Mendelian Green Cotyledon Gene in Soybean Encodes a Small Subunit of Photosystem II. &nbsp;Plant Physiol. 173:2138-2147.<\/p>\n\n\n\n<p>Nishimura K, Kato Y, Sakamoto W.(2017) Essentials of Proteolytic Machineries in Chloroplasts. Mol Plant. 16:30166-6.<\/p>\n\n\n\n<p><strong>2016<\/strong><\/p>\n\n\n\n<p>Matsushima, R., Maekawa, M., Kusano, M., Tomita, K., Kondo, H., Nishimura, H., Crofts N., Fujita N. and Sakamoto W. (2016) Amyloplast membrane protein SUBSTANDARD STARCH GRAIN6 controls starch grain size in rice endosperm. Plant Physiology 170: 1445-1459.<\/p>\n\n\n\n<p>Toyosawa, Y., Kawagoe, Y., Matsushima, R., Crofts, N., Ogawa, M., Fukuda, M., Kumamaru, T., Okazaki, Y., Kusano, M., Saito, K., Toyooka, K., Sato, M., Ai, Y., Jane, J.-L., Nakamura, Y. and Fujita, N.(2016) Deficiency of Starch Synthase IIIa and IVb alters starch granule morphology from polyhedral to spherical in rice endosperm. Plant Physiology 170: 1225-1270<\/p>\n\n\n\n<p>\u5742\u672c\u4e98 \u5149\u5408\u6210\u306e\u52b9\u7387\u5411\u4e0a\u3068\u30b9\u30fc\u30d1\u30fc\u30d0\u30a4\u30aa\u30de\u30b9.(2016)\u30b9\u30fc\u30d1\u30fc\u30d0\u30a4\u30aa\u30de\u30b9:\u690d\u7269\u306b\u5b66\u3076\u3001\u690d\u7269\u3092\u6d3b\u304b\u3059\uff08\u798f\u7530\u88d5\u7a42\u3001\u7a32\u7530\u306e\u308a\u3053\u7de8\uff09. Pp19-39 \u6176\u61c9\u5927\u5b66\u51fa\u7248\u4f1a<\/p>\n\n\n\n<p>Zhang L, Kusaba M, Tanaka A, Sakamoto W.(2016) Protection of Chloroplast Membranes by VIPP1 Rescues Aberrant Seedling Development in Arabidopsis nyc1 Mutant. Front Plant Sci.28;7:533<\/p>\n\n\n\n<p>Zhang L, Kondo H, Kamikubo H, Kataoka M, Sakamoto W.(2016) VIPP1 Has a Disordered C-Terminal Tail Necessary for Protecting Photosynthetic Membranes against Stress.Plant Physiol. 171:1983-95<\/p>\n\n\n\n<p>Nishimura K, Kato Y, Sakamoto W.(2016) Chloroplast Proteases: Updates on Proteolysis within and across Suborganellar Compartments. Plant Physiol. 171:2280-93<\/p>\n\n\n\n<p>Tominaga J, Mizutani H, Horikawa D, Nakahara Y, Takami T, Sakamoto W, Sakamoto A, Shimada H.(2016) Rice CYO1, an ortholog of Arabidopsis thaliana cotyledon chloroplast biogenesis factor AtCYO1, is expressed in leaves and involved in photosynthetic performance. J Plant Physiol. 207:78-83.<\/p>\n\n\n\n<p><strong>2015<\/strong><\/p>\n\n\n\n<p>Matsushima R, Maekawa M, Sakamoto W. (2015) Geometrical formation of compound starch grains in rice implements voronoi&nbsp;diagram. Plant Cell Physiol. 56:2150-2157. doi: 10.1093\/pcp\/pcv123.<\/p>\n\n\n\n<p>Oikawa, K., Matsunaga, S., Mano, S., Kondo, K., Yamada, K., Hayashi, M., Kagawa, T., Kadota, A., Sakamoto, W., Higashi, S., Watanabe, M., Mitsui, T., Shigemasa, A., Takanori Iino, T., Hosokawa, Y. and Nishimura, N. (2015)\u3000Physical interaction between peroxisomes and chloroplasts elucidated by in situ laser analysis. Nature Plants 1, 15035 \u200bdoi:10.1038\/nplants.2015.57<\/p>\n\n\n\n<p>Kato, Y., Ozawa, SI., Takahashi, Y. and Sakamoto W. (2015) D1 fragmentation in photosystem II repair caused by photo-damage of a two-step model. Photosynth Res.&nbsp;<span class=\"Apple-style-span\">126:409-416. doi: 10.1007\/s11120-015-0144-7<\/span><\/p>\n\n\n\n<p>Zhang, L., and Sakamoto, W. (2015) Possible function of VIPP1 in maintaining chloroplast membranes. Biochim Biophys Acta.1847:831-7. doi: 10.1016\/j.bbabio.2015.02.013.<\/p>\n\n\n\n<p>Kamau, PK., Sano, S., Takami, T., Matsushima, R., Maekawa, M. and Sakamoto, W. (2015) A mutation in GIANT CHLOROPLAST encoding a PARC6 homolog affects spikelet fertility in rice. Plant Cell Physiol. 56:977-91. doi: 10.1093\/pcp\/pcv024.<\/p>\n\n\n\n<p><strong>2014<\/strong><\/p>\n\n\n\n<p>Kato, Y. and Sakamoto, W. (2014) Phosphorylation of photosystem II core proteins prevents undesirable cleavage of D1 and contributes to the fine-tuned repair of photosystem II. Plant J. 79:312-321.doi: 10.1111\/tpj.12562<\/p>\n\n\n\n<p>Borg, M., Rutley, N., Kagale, S., Hamamura,Y., Gherghinoiu, M., Kumar, S., Sari, U., Esparza-Franco, MA., Sakamoto, W., Rozwadowski, K., Higashiyama, H.andTwell, D. (2014) An EAR-Dependent Regulatory Module Promotes Male Germ Cell Division and Sperm Fertility in Arabidopsis. Plant Cell 26:2098-2113. &nbsp;tpc.114.124743.<\/p>\n\n\n\n<p>\u771f\u91ce\u660c\u4e8c\u30fb\u5c71\u7530\uff08\u5f8c\u85e4\uff09\u5fd7\u91ce\u30fb\u5742\u672c\u4e98 (2014) \u53d7\u7cbe\u3068\u30aa\u30eb\u30ac\u30cd\u30e9\uff1a\u30df\u30c8\u30b3\u30f3\u30c9\u30ea\u30a2\u3001\u30d7\u30e9\u30b9\u30c1\u30c9\u3001\u30da\u30eb\u30aa\u30ad\u30b7\u30bd\u30fc\u30e0. \u52d5\u690d\u7269\u306e\u53d7\u7cbe\u5b66\uff08\u6fa4\u7530\u5747\u7de8\uff09\u5316\u5b66\u540c\u4eba.pp.301-317.<\/p>\n\n\n\n<p>Sakamoto, W. and Takami, T. (2014) Nucleases in higher plants and their possible involvement in DNA degradation during leaf senescence.J.Exp.Bot. 65:3835-3834.&nbsp;doi: 10.1093\/jxb\/eru091.<\/p>\n\n\n\n<p>Adam, Z. and Sakamoto, W. (2014) Plastid proteases.PlastidBiology (edsTheg, S.andWollman, F.-A.) Advances in Plant Biology (ed. Harada, J.), Springer, 5:359-389.<\/p>\n\n\n\n<p>Shibata, M., Oikawa, K., Yoshimoto, K., Kondo, M., Mano, S., Yamada, K., Hayashi, M., Sakamoto, W., Ohsumi, Y., and Nishimura, M. Plant autophagy is responsible for peroxisomal transition and plays an important role in the maintenance of peroxisomal quality. Autophagy, 10: 936-937.<\/p>\n\n\n\n<p>Wudick, M.M., Luu, D.-T., Tournaire-Roux, C., Sakamoto, W., and Maurel, C. (2014) Vegetative and sperm cell-specificaquaporinsofArabidopsishighlightthevacuolarequipmentofpollenand contribute to plant reproduction. Plant Physiol., 164: 1697-1706.<\/p>\n\n\n\n<p>Matsushima, R., Maekawa, M., Kusano, M., Kondo, H., Fujita, N., Kawagoe, Y., and Sakamoto, W. (2014) Amyloplast-Localized SUBSTANDARD STARCH GRAIN4 Protein Influences the Size of Starch Grains in Rice Endosperm. Plant Physiol. 164: 623-636.<\/p>\n\n\n\n<p>Asai H, Abe N, Matsushima R, Crofts N, Oitome NF, Nakamura Y, Fujita N. (2014)&nbsp;Deficiencies in both starch&nbsp;synthase&nbsp;IIIa and branching enzyme IIb lead to a significant increase in&nbsp;amylose&nbsp;in SSIIa-inactive japonica rice seeds.&nbsp;J Exp Bot. 65:5497-5507.doi: 10.1093\/jxb\/eru310.<\/p>\n\n\n\n<p>\u52a0\u85e4\u88d5\u4ecb\u30fb\u5742\u672c \u4e98 (2014) \u5149\u5408\u6210\u306e\u5149\u963b\u5bb3:\u5149\u5316\u5b66\u7cfbII\u306e\u640d\u50b7\u3068\u4fee\u5fa9\u306e\u5206\u5b50\u30e1\u30ab\u30cb\u30ba\u30e0. \u5149\u5408\u6210\u7814\u7a76\u3068\u7523\u696d\u5fdc\u7528\u6700\u524d\u7dda\u3002NST pp.97-107.<\/p>\n\n\n\n<p>\u8db3\u7acb\u592a\u90ce\u30fb\u5c71\u6975\u5bff\u4e00\u30fb\u5c71\u6839\u88d5\u7f8e\u30fb\u5742\u672c \u4e98\u30fb\u5c71\u79d1\u5343\u91cc\u30fb\u5c71\u8d8a \u8a00. (2014)\u751f\u7269\u5b66\u3068\u30a2\u30d5\u30ea\u30ab\u306e\u672a\u6765. \u30a2\u30d5\u30ea\u30ab\u7814\u7a76 85:33-50<\/p>\n\n\n\n<p><strong>2013<\/strong><\/p>\n\n\n\n<p>Shibata, M., Oikawa, K., Yoshimoto, K., Kondo, M., Mano, S., Yamada, K., Hayashi, M., Sakamoto, W., Ohsumi, Y., and Nishimura. M. (2013) Highly Oxidized Peroxisomes Are Selectively Degraded via Autophagy in Arabidopsis. Plant Cell 25: 4967-4983<\/p>\n\n\n\n<p>Sakamoto, W., Miura, E., and Kato, Y. (2013) A novel link between chloroplast developmentandstressresponselessonedbyleaf-variegated mutant. In Photosynthesis Research for Food, Fuel and Future. 15th International Conference on Photosynthesis. (eds. Kuang, T., Lu, C., and Zhang, L.), pp. 669-673, Springer.<\/p>\n\n\n\n<p>Zhang, L., Kato, Y., Saigo, K., Vothknecht, U.C., and Sakamoto, W. (2013) The lattice-like structure observed by Vipp1-GFP in Arabidopsis chloroplasts. In Photosynthesis Research for Food, Fuel and Future. 15th International Conference on Photosynthesis. (eds. Kuang, T., Lu, C., and Zhang, L.), pp. 394-397, Springer.<\/p>\n\n\n\n<p>\u52a0\u85e4\u88d5\u4ecb\u30fb\u5742\u672c\u3000\u4e98 (2013) \u5149\u963b\u5bb3\u306b\u304a\u3051\u308b\u5149\u5316\u5b66\u7cfbII\u53cd\u5fdc\u4e2d\u5fc3\u30bf\u30f3\u30d1\u30af\u8ceaD1\u306e\u5206\u89e3\u3068\u8449\u7dd1\u4f53\u30d7\u30ed\u30c6\u30a2\u30fc\u30bc. \u5149\u5408\u6210\u7814\u7a76 23(2): 79-85.<\/p>\n\n\n\n<p>Kato, Y.andSakamoto, W. (2013) Plastid protein degradation during leaf development and senescence: Role of protease and chaperones. In Chloroplast Development during Leaf Growth and Senescence, Advances in Photosynthesis and Respiration Vol. 36, pp453-477 (Eds.Biswal, B., Krupinska, K., and Biswal, U.C.), Springer (ISBN 978-94-007-5723-3).<\/p>\n\n\n\n<p>Matsushima R., Yamashita J., Kariyama, S., Enomoto, T., and Sakamoto, W. (2013) A phylogenetic re-evaluationofmorphologicalvariationsofstarchgrainsamong Poaceae species.J.Appl.Glycosci. 60, 37-44.<\/p>\n\n\n\n<p>Nagai M, Ohnishi M, Uehara T, Yamagami M, Miura E, Kamakura M, Kitamura A, Sakaguchi SI, Sakamoto W, Shimmen T, Fukaki H, Reld RJ, Furukawa A, Mimura T. (2013) Ion gradients inxylemexudateandguttationfluidrelatedtotissue ion levels along primary leaves of barley. Plant Cell Environ. 36:1826-1837.<\/p>\n\n\n\n<p>Yamatani H, Sato Y, Masuda Y, Kato Y, Morita R, Fukunaga K, Nagamura Y, Nishimura M, Sakamoto W, Tanaka A, Kusaba M. (2013) NYC4, the rice ortholog of Arabidopsis THF1, is involved in the degradation of chlorophyll-protein complexes during leaf senescence. Plant J. 74: 652-662.<\/p>\n\n\n\n<p>Zhang L, Sakamoto W. (2013) Possible function of VIPP1inthylakoids: Protection but not formation?&nbsp;Plant Signaling Behavior 8: e22860.<\/p>\n\n\n\n<p>Kato Y, Sakamoto W. (2013) Possible compensatory role among chloroplast proteases under excess-light stress condition.&nbsp;Plant Signaling Behavior 8: e23198.<\/p>\n\n\n\n<p><strong>2012<\/strong><\/p>\n\n\n\n<p>Nakano RT, Matsushima R, Nagano AJ, Fukao Y, Fujiwara M, Kondo M, Nishimura M, Hara-Nishimura I. (2012) ERMO3\/MVP1\/GOLD36 is involved in a cell type-specific mechanism for maintaining ER morphology in <em>Arabidopsis thaliana<\/em> PLoS ONE e49103<\/p>\n\n\n\n<p>Zhang L, Kato Y, Otters S, Vothknecht UC, Sakamoto W. (2012) Essential Role of VIPP1 in Chloroplast Envelope Maintenance in <em>Arabidopsis <\/em>Plant Cell 24: 3695-3707<\/p>\n\n\n\n<p>Kato Y, Sun X, Zhang L, Sakamoto W. (2012)&nbsp;Cooperative D1 Degradation in the Photosystem II Repair Mediated by Chloroplastic Proteases in Arabidopsis.&nbsp;Plant Physiol.&nbsp;&nbsp;159:1428-1439<\/p>\n\n\n\n<p>MatsushimaR. (2012) Applications of a rapid method to observe starch grains. Bulletin of Applied Glycoscience 2: 147-149<\/p>\n\n\n\n<p>Tang LY, Matsushima R, Sakamoto W. (2012)&nbsp;Mutations defective in ribonucleotide reductase activityinterferewithpollenplastidDNAdegradationmediatedbyDPD1exonuclease. Plant J.70:637-49<\/p>\n\n\n\n<p>Kato Y, Kouso T, Sakamoto W. (2012)&nbsp;Variegated tobacco leaves generated by chloroplast FtsH suppression: implication of FtsH function in the maintenance of thylakoid membranes.<br>Plant Cell Physiol. 53: 391-404.<\/p>\n\n\n\n<p><strong>2011<\/strong><\/p>\n\n\n\n<p>Matsushima, R., Tang, L. Y., Zhang L., Yamada, H., Twell, D.andSakamoto, W. (2011)&nbsp;&nbsp;A conserved, Mg2+-dependentexonucleasedegradesorganelleDNA during Arabidopsis pollen development. Plant Cell 23: 1608-24.<\/p>\n\n\n\n<p>Ozawa, R., Matsushima, R., Maffei, M.E.andTakabayashi, J. (2011)&nbsp;Interaction between Phaseolus plants and two strains of Kanzawa spider mites. Journal of Plant Interactions 6: 125-128.<\/p>\n\n\n\n<p>Tang, L.Y.andSakamoto, W. (2011)&nbsp;&nbsp;Tissue-specific organelle DNA degradation mediated by DPD1exonuclease. Plant Signaling Behavior 6: 1391-1393.<\/p>\n\n\n\n<p>Sakamoto, W., Miura, E., and Kato, Y. (2011) A novel link between chloroplast development andstressresponselessonedbyleaf-variegated mutant. Proceedings of the 15th International Congress on Photosynthesis (in press)<\/p>\n\n\n\n<p>Zhang, L., Kato, Y., Saigo, K., Vothknecht, U.C., and Sakamoto, W. (2011) The lattice-like structure observed by Vipp1- GFP in Arabidopsis chloroplasts. Proceedings of the 15th International Congress on Photosynthesis (in press)<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<p><strong>2010<\/strong><\/p>\n\n\n\n<p>Zhang, D., Kato, Y., Zhang, L., Fujimoto, M., Tsutsumi, N., Sodmergen, Sakamoto, W. (2010) The FtsH Protease Heterocomplex in Arabidopsis: Dispensability of Type-B Protease Activity for Proper Chloroplast Development. Plant Cell, Nov;22(11):3710-2.<\/p>\n\n\n\n<p>Saika, H., Sakamoto, W., Maekawa, M., Toki, S. (2010) Highly efficient visual selection of transgenic rice plants using green fluorescentproteinoranthocyaninsyntheticgenes. Plant Biotech., in press.<\/p>\n\n\n\n<p>Matsushima, R., Maekawa, M., Fujita, N., Sakamoto, W. (2010) A rapid, direct observation method to isolate mutants with defects in starch grain morphology in rice. Plant Cell Physiol., 51: 728-741.<\/p>\n\n\n\n<p>Piechota, J., Kolodziejczak, M., Juszczak, I., Sakamoto, W., Janska, H. (2010) Identification and characterization of high-molecular-weight complexes by m-AAAproteasesandprohibitinsinmitochondriaof Arabidopsis thaliana. J. Biol. Chem., 285: 12512-12521.<\/p>\n\n\n\n<p>Kato, Y., Sakamoto, W. (2010) New insights into the types and function ofproteasesinplastids. Intl. Rev.Mol. Cell Biol., 161: 185-218.<\/p>\n\n\n\n<p>Miura, E., Kato, Y., Sakamoto, W. (2010) Comparative transcriptome analysis of green\/white variegated sectors in Arabidopsis yellow variegated2: responses to oxidative and other stresses in white sectors.J.Exp.Bot., 61: 2433-2445.<\/p>\n\n\n\n<p>Miura E., Kato, Y., and Sakamoto, W. (2010) Reactive oxygen species derived from impaired quality control of photosystem II are irrelevant to plasma-membrane NADPH oxidases. Plant Signaling Behavior. 5: 264-266.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<p><strong>2009<\/strong><\/p>\n\n\n\n<p>Kato Y, Miura E, Ido K, Ifuku K, Sakamoto W. (2009) The variegatedmutantslackingchloroplasticFtsHsaredefective in D1 degradation and accumulate reactive oxygen species.Plant Physiol. 151(4):1790-801.<\/p>\n\n\n\n<p>Tang LY, Nagata N, Matsushima R, Chen Y, Yoshioka Y, Sakamoto W.(2009) Visualizationofplastidsinpollen grains: involvement of FtsZ1inpollenplastiddivision.Plant Cell Physiol. 50(4):904-8.<\/p>\n\n\n\n<p>Sakamoto W, Uno Y, Zhang Q, Miura E, Kato Y, Sodmergen. (2009) Arresteddifferentiationofproplastidsintochloroplastsin variegated leaves characterized byplastidultrastructureandnucleoidmorphology. Plant Cell Physiol. 50(12):2069-83.<\/p>\n\n\n\n<p>Kato Y, Sakamoto W. (2009) Protein quality control in chloroplasts: a current model of D1 protein degradation in the photosystem II repair cycle.<br>J Biochem. 146(4):463-9. Review.<\/p>\n\n\n\n<p>Zhang L, Wei Q, Wu W, Cheng Y, Hu G, Hu F, Sun Y, Zhu Y, Sakamoto W, Huang J. (2009) Activation of the heterotrimeric G protein alpha-subunit GPA1suppressestheftsh-mediated inhibition of chloroplast development in Arabidopsis. Plant J. 58(6):1041-53.<\/p>\n\n\n\n<p>Gibala M, Kicia M, Sakamoto W, Gola EM, Kubrakiewicz J, Smakowska E, Janska H. (2009) The lack of mitochondrial AtFtsH4 protease alters Arabidopsis leaf morphology at the late stage of rosette development under short-day photoperiod. Plant J. 59(5):685-99.<\/p>\n\n\n\n<p>Nakano RT, Matsushima R, Ueda H, Tamura K, Shimada T, Li L, Hayashi Y, Kondo M, Nishimura M, Hara-NishimuraI.(2009) GNOM-LIKE1\/ERMO1 and SEC24a\/ERMO2 are required for maintenance of endoplasmic reticulum morphology in Arabidopsis thaliana. Plant Cell. :3672-85.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<p><strong>2008<\/strong><\/p>\n\n\n\n<p>MatsushimaR, Hamamura Y, Higashiyama T, Arimura S, Sodmergen, Tsutsumi N, Sakamoto W.(2008) Mitochondrial dynamics inplantmalegametophytevisualizedbyfluorescent live imaging. Plant Cell Physiol. 49(7):1074-83.<\/p>\n\n\n\n<p>Matsushima R, Hu Y, Toyoda K, Sodmergen, Sakamoto W. (2008) The model plant Medicago truncatula exhibits biparentalplastidinheritance.<br>Plant Cell Physiol. 49(1):81-91.<\/p>\n\n\n\n<p>Yoshida K, Watanabe C, Kato Y, Sakamoto W, Noguchi K. (2008) Influenceofchloroplasticphoto-oxidative stressonmitochondrial alternative oxidase capacityandrespiratory properties: a case study with Arabidopsis yellow variegated 2. Plant Cell Physiol. 49(4):592-603.<\/p>\n\n\n\n<p>Shih CH, Chu H, Tang LK, Sakamoto W, Maekawa M, Chu IK, Wang M, Lo C. (2008) Functional characterization of key structural genes in rice flavonoid biosynthesis.Planta. 228(6):1043-54.<\/p>\n\n\n\n<p>Kmiec-Wisniewska B, Krumpe K, Urantowka A, Sakamoto W, Pratje E, Janska H. (2008) Plant mitochondrial rhomboid, AtRBL12,hasdifferentsubstratespecificityfromitsyeast counterpart. Plant Mol Biol. 68(1-2):159-71.<\/p>\n\n\n\n<p>Arimura S, Fujimoto M, Doniwa Y, Kadoya N, Nakazono M, Sakamoto W, Tsutsumi N. (2008) Arabidopsis ELONGATED MITOCHONDRIA1 is required for localization of DYNAMIN-RELATED PROTEIN3A to mitochondrial fission sites. Plant Cell. 20(6):1555-66.<\/p>\n\n\n\n<p>Sakamoto W, Miyagishima S, Jarvis P (2008) Chloroplast biogenesis: Plastid division, inheritance, regulation, proteinimportandproteome. The Arabidopsis Book, http:\/\/www.aspb.org\/publications\/arabidopsis\/<\/p>\n\n\n\n<p>Sugimoto M, Sakamoto W, Fujitani Y (2008) Localization and expression of serine racemase in Arabidopsis thaliana. Amino Acids, 36(3):587-90<\/p>\n\n\n\n<p>Diaz C, Lema\u00eetre T, Christ A, Azzopardi M, Kato Y, Sato F, Morot-Gaudry JF, Le Dily F, Masclaux-Daubresse C. (2008) Nitrogenrecyclingandremobilizationaredifferentiallycontrolledbyleafsenescence and development stage in Arabidopsis under low nitrogen nutrition.Plant Physiol. 147(3):1437-49.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<p><strong><a title=\"Before 2007\" href=\"http:\/\/www.rib.okayama-u.ac.jp\/saka\/?page_id=51\">Before 2007<\/a><\/strong><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>2025 Sakamoto, W. Thylakostasis: Key Factors in Thylakoid Membrane Organization with Emphasis on Biogenesis an &hellip; <a href=\"https:\/\/www.rib.okayama-u.ac.jp\/saka\/list-of-publications\/\">\u7d9a\u304d\u3092\u8aad\u3080 <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"sidebar-page.php","meta":{"footnotes":""},"class_list":["post-23","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/pages\/23","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/comments?post=23"}],"version-history":[{"count":45,"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/pages\/23\/revisions"}],"predecessor-version":[{"id":2742,"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/pages\/23\/revisions\/2742"}],"wp:attachment":[{"href":"https:\/\/www.rib.okayama-u.ac.jp\/saka\/wp-json\/wp\/v2\/media?parent=23"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}