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Plant Response group

2023

  1. Y. Sakihama*, T. Kato, S. Sawatdee, Y. Yakushi, J. Asano, H. Hayashi, Y. Goto, M. Hashimoto, and Y. Hashidoko. Isolation of High-purity betanin from red beet and elucidation of its antioxidant activity against peroxynitrite: an in vitro study. International Journal of Molecular Sciences, 24, 15411 (2023); https://doi.org/10.3390/ijms242015411

  2. S. Sawatdee, T. Jarunglumlert, P. Pavasant, Y. A.E. Flood and C. Prommuak. Effect of mixed light emitting diode spectrum on antioxidants content and antioxidant activity of red lettuce grown in a closed soilless system. BMC Plant Biology, 23, 351 (2023); doi:10.1186/s12870-023-04364-y.

  3. H. Wakabayashi, K. Sugiyama, S. Suzuki, M. Hashimoto, M.J. Barwood, Influence of acute beetroot juice supplementation on cold-induced vasodilation and fingertip rewarming, European Journal of Applied Physiology,123, 495–507 (2023); DOI: 10.1007/s00421-022-05071-6

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2021

  1. Y. Sakihama and Hideo Yamasaki. Phytochemical Antioxidants: Past, Present and Future In Antioxidants. Ed. Viduranga Yashasvi Waisundara, IntechOpen, (2021). DOI: 10.5772/intechopen.95627.　

  2. M. Hane, H.C. Wijaya, Y.A. Nyon, Y. Sakihama,∗ M. Hashimoto,∗ H. Matsuura and Y. Hashidoko. Phenazine-1-carboxylic acid (PCA) produced by Paraburkholderia phenazinium CK-PC1 aids postgermination growth of Xyris complanata seedlings with germination induced by Penicillium rolfsii Y-1, Bioscience, Biotechnology, and Biochemistry, 85, 77-84 (2021); DOI: 10.1093/bbb/zbaa060

 

2020~

  1. D.A. Suroto, S. Kitani, K.T. Miyamoto, M. Arai, H. Ikeda, and T. Nihira. Activation of cryptic phthoxazolin A production in Streptomyces avermitilis by the disruption of autoregulator-receptor homologue AvaR3. Journal of Bioscience Bioengineering, (2017), http://dx.doi.org/10.1016/j.jbiosc. 2017.06.014.

  2. Y. Yamashita, M. Ota, Y. Inoue, Y. Hasebe, M. Okamoto, T. Inukai, C. Masuta, Y. Hashidoko, M. Kojima, H. Sakakibara, Y. Inage, K. Takahashi, T. Yoshihara, H. Matsuura. Chemical promotion of endogenous amounts of ABA in Arabidopsis thaliana by a natural product, theobroxide. Plant and Cell Physiology, 57, 986-999 (2016); DOI:10.1093/pcp/pcw037.

  3. H. Yamasaki, N.S. Watanabe, M.F. Cohen. An overview of methods in plant NO research: Why do we always need to use multiple methods? In: Methods in Molecular Biology: Plant Nitric Oxide: Methods & Protocol (K.J. Gupta ed.), Humana Press. Totowa, NJ. 1424:1-14 (2015).

  4. S.P. Putri, K. Ishido, H. Kinoshita, S. Kitani, F. Ihara, Y. Sakihama, Y. Igarashi, and T. Nihira, Production of antioomycete compounds active against the phytopathogens Phytophthora sojae and Aphanomyces cochlioides by clavicipitoid entomopathogenic fungi. Journal of Bioscience Bioengineering, 117, 557-562 (2014); DOI:10.1016/j.jbiosc.2013.10.014.

  5. M. Wang, T. Takayama, and Y. Hashidoko, Effects of different classes of attractants, cochliophilin A and N-(E)-feruloyl-4-O-methyldopamine, on the response of Aphanomyces cochlioides zoospores in their chemo- attraction and activation of motility linked with intracellular cAMP. Journal of Pesticide Science 38, 181-187 (2013); DOI:10.1584/jpestics.D13-034.

  6. Y. Sakihama, M. Maeda, M. Hashimoto, S. Tahara and Y. Hashidoko. Beetroot betalain inhibits peroxynitrite-mediated tyrosine nitration and DNA strand cleavage. Free Radical Research 46, 93-99 (2012); DOI:10.3109/10715762.2011.641157.

  7. M.T. Islam, M. Sakasai, Y. Hashidoko, A. Deora, and S. Tahara. Composition of culture medium influences zoosporogenesis and differentiation of Aphanomyces cochlioides. Journal of General Plant Pathology 73, 324-329 (2007); DOI:https://doi.org/10.1007/s10327-007-0026-8.　

  8. B.M. Tyler et al. (53人中40番目), Phytophthora genome sequences uncover evolutionary origins and mechanisms of pathogenesis. Science, 313, 1261-1266 (2006); DOI:10.1126/science.1128796.

  9. M.S. Connolly, , V. Phuntumart, Y. Jiang, F. Warren, L. Mourant and P.F. Morris, Heterologous expression of a pleiotropic drug resistance transporter from Phytophthora sojae in yeast transporter mutants. Current Genetics 48, 356-365 (2005); DOI:10.1007/s00294-005-0015-4.

  10. Y. Sakihama, T. Shimai, M. Sakasai, T. Ito, Y. Fukushi, Y. Hashidoko and S. Tahara. A photoaffinity probe designed for host-specific signal flavonoid receptors in phytopathogenic Peronosporomycete zoospores of Aphanomyces cochlioides. Archives of Biochemistry and Biophysics 432, 145-151 (2004); DOI:10.1016/j.abb.2004.09.017.

  11. Y. Sakihama, R. Tamaki, H. Shimoji, T. Ichiba, Y. Fukushi, S. Tahara, and H. Yamasaki. Enzymatic nitration of phytophenolics: evidence for peroxynitrite-independent nitration of plant secondary metabolites. FEBS Letters 533, 377-380 (2003); DOI:10.1016/S0014-5793(03)01059-7.

  12. Y. Sakihama, S. Murakami and H. Yamasaki. Involvement of nitric oxide in the mechanism for stomatal opening in Vicia faba leaves. Biologia Plantarum. 46, 117-119 (2003); DOI:10.1023/A:1022378621030.

  13. M.F. Cohen, Y.C. Takagi, T. Ichiba and H. Yamasaki. Synergistic effect of deoxyanthocyanins from the symbiotic fern Azolla on hrm A gene induction in the cyanobacterium Nostoc punctiforme. Molecular Plant-Microbe Interactions. 15, 875-882 (2002); DOI:10.1094/MPMI.2002.15.9.875.

  14. Y. Sakihama, M.F. Cohen, S.C. Grace and H. Yamasaki. Plant phenolic antioxidant and prooxidant activities: phenolics-induced oxidative damage mediated by metals in plants. Toxicology. 177, 67-80 (2002); DOI: 10.1016/S0300-483X(02)00196-8

  15. S. Takahashi, A. Tamashiro, Y. Yamamoto, Y. Kawamitsu and H. Yamasaki. High-susceptibility of photosynthesis to photoinhibition in the tropical plant Ficus microcarpa L. f. cv. Golden Leaves. BMC Plant Biology. 2, 2 (2002); DOI:https://doi.org/10.1186/1471-2229-2-2.

  16. M. Papina, C. Bena, R. van Woesik and H. Yamasaki. Separation of highly fluorescent proteins by SDS-PAGE in Acroporidae corals. Comparative Biochemistry and Physiology (2002); DOI:10.1016/S1096-4959(02)00025-8.

  17. Y. Sakihama, S. Nakamura and H. Yamasaki. Nitric oxide production mediated by nitrate reductase in the green alga Chlamydomonas reinhardtii: an alternative NO production pathway in photosynthetic organisms. Plant and Cell Physiology. 43, 290-297 (2002). DOI:10.1093/pcp/pcf034.

  18. Y. Sakihama and H. Yamasaki. Lipid peroxidation induced by phenolics in conjunction with aluminum ions. Biologia Plantarum 45, 249-254 (2002); DOI:10.1023/A:1015152908241.

  19. H. Yamasaki, H. Shimoji, Y. Ohshiro and Inhibitory effects of nitric oxide on oxidative phosphorylation in plant mitochondria. Nitric Oxide 5, 261-270 (2001); DOI10.1006/niox.2001.0353.

  20. Y. Sakihama, J. Mano, S. Sano, K. Asada and H. Yamasaki. Reduction of phenoxyl radicals mediated by monodehydroascorbate reductase. Biochemical and Biophysical Research Communications 279, 949-954 (2000); DOI10.1006/bbrc.2000.4053.

  21. H. Yamasaki and Simultaneous production of nitric oxide and peroxynitrite by plant nitrate reductase: in vitro evidence for the NR-dependent formation of active nitrogen species. FEBS Letters 468, 89-92 (2000); DOI10.1016/S0014-5793(00)01203-5.

  22. H. Yamasaki, and S. Takahashi. An alternative pathway for nitric oxide production in plants: new features of an old enzyme. Trends in Plant Science 4, 128-129 (1999); DOI10.1016/S1360-1385(99)01393-X.

  23. H. Yamasaki, and N. Ikehara. Flavonoid-peroxidase reaction as a detoxification mechanism of plant cells against H2O2. Plant Physiology 115, 1405-1412 (1997); DOI10.1104/pp.115.4.1405.

  24. H. Yamasaki, H. Uefuji and Bleaching of the red anthocyanin induced by superoxide radical. Archives of Biochemistry and Biophysics 332, 183-186 (1996); DOI10.1006/abbi.1996.0331.

  25. ・池原規勝・山崎秀雄. ヤドリフカノキSchefflera arboricola Hayata の生葉中フラボノール. 沖縄生物学会誌 33, 43-48 (1995).

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