九州大学-研究者情報 [森元聡 (教授) 薬学研究院臨床薬学部門]

薬用植物の細胞分裂メカニズムの解明
キーワード：薬用植物、細胞分裂
2002.05.

植物の生体防御に関する研究
キーワード：植物、生体防御
1995.04.

大麻成分の生合成に関する研究
キーワード：大麻、生合成
1993.04.

腸管出血性大腸菌感染症の征圧に向けた包括的研究
2015.04～2016.03, 代表者：藤井潤, 鳥取大学医学部細菌学分野
出血性大腸菌感染症に著効を示す生薬成分の解明.

中性子構造解析を利用した生物有機化学的研究
2015.04～2016.03, 代表者：玉田太郎, 日本原子力研究開発機構
大麻成分の生合成酵素の立体構造を中性子散乱法を用いて解析し、酵素反応のメカニズムを解明する。.

中性子構造解析を利用した生物有機化学的研究
2006.04～2007.03, 代表者：黒木良太, 日本原子力研究開発機構
大麻成分の生合成酵素の立体構造を中性子散乱法を用いて解析し、酵素反応のメカニズムを解明する。.

主要著書

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主要原著論文

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1.	＃Nuntawong, P., ＃Ochi, A., Chaingam, J., ＠Tanaka, H., ＠Sakamoto, S., ＠Morimoto, S., The colloidal gold nanoparticle based-lateral flow immunoassay for fast and simple detection of plant-derived doping agent, higenamine.”, Drug Test Anal., 13, 762-769, 2021.04.
2.	Sakamoto, S., Uchiyama, H., Yusakul, G., Kyokong, N., Pongkitwitoon, B., Putalun, W., Tanaka, H., Morimoto, S., Open sandwich fluorescence-linked immunosorbent assay for detection of soy isoflavone glycosides, Food Chem., 391, 129829, 2021.11.
3.	＃Minami, K., ＠Yusakul, G., ＠Fujii, S., ＠Putalun, W., ＠Tanaka, H., ＠Sakamoto, S., ＠Morimoto, S., Rapid magnetic particles-based enzyme immunoassay for the quality control of Glycyrrhiza spp. based on glycyrrhizin content., Fitoterapia,, 148, 104794, 2021.01.
4.	Nuntawong P, Horikawa T., Ochi A, Wada S. Tsuneura Y, Tanaka H, Sakamoto S, Morimoto S., A monoclonal antibody-based indirect competitive enzyme-linked immunosorbent assay to quantify swertiamarin and its related compounds in Swertia japonica Makino, Phytochem. Anal., in press , 2020.09.
5.	Nuntawong P, Lohseethong K, Juengwatanatrakul T, Yusakul G, Putalun W, Tanaka H, Sakamoto S, Morimoto, S., Competitive immunochromatographic test strips for the rapid semi-quantitative analysis of the biologically active bitter glycoside, amarogentin, J. Immunoassay Immunochem., in press, 2020.09.
6.	Sakamoto S, Eto R, Nuntawong P, Yusakul G, Juengwatanatrakul T, Putalun W, Fujii S , Tanaka H, Morimoto S , Kwakhurin-magnetic particles conjugates enable fast enzyme immunoassay for the detection of kwakhurin in Pueraria candollei, Pytochemical Analysis, in press, 2020.06.
7.	Yusakul, G., Sakamoto, S., Chanpokapaiboon, K., Tanaka, H., Morimoto, S, Preincubation format for a sensitive immunochromatographic assay for monocrotaline, a toxic pyrrolizidine alkaloid., Phytochem. Anal., 30, 6, 600-608, 2019.11.
8.	Yusakul, G., Sakamoto, S., Tanaka, H., Morimoto, S., Modification of first constant domain of heavy chain (CH1) enabled effective folding of functional anti-forskolin antigen-binding fragment (Fab) for sensitive quantitative analysis., Biotechnol. Prog., 35, 4, e2822, 2019.07.
9.	Yusakul, G., Togita, R., Minami, K., Chanpokapaiboon, K., Juengwatanatrakul, T., Putalun, W., Tanaka, H., Sakamoto, S., Morimoto, S, An indirect competitive enzyme-linked immunosorbent assay toward standardization of Pueraria candollei based on its unique isoflavonoid, kwakhurin., Fitoterapia, 133, 23-28, 2019.03.
10.	Sakamoto, S., Wada, S., Morita, Y., Yamaguchi, T., Tanaka, H., Morimoto, S., Magnetic particles-based enzyme immunoassay for rapid determination of secoiridoid glycoside, amarogentin, Talanta, in press, 2019.01.
11.	Sakamoto S.,Wada, S., Tanaka, H., Morimoto, S., Sensitive quantitative analysis of the bitter glycoside, amarogentin by specific monoclonal antibody-based indirect competitive enzyme-linked immunosorbent assay, RSC Advances, in press, 2018.05.
12.	＃Pongkitwitoon, B., Sakamoto, S., Nagamitsu, R., Putalun W., Tanaka, H., Morimoto, S., A monoclonal antibody-based enzyme-linked immunosorbent assay for determination of homoharringtonine, Planta Medica, in press, 2018.02.
13.	Sakamoto S, Miyamoto T, Usui K, Tanaka H, Morimoto S, Sodium-periodate Mediated Harringtonine Derivatives and Their　Antiproliferative Activity against HL-60 Acute Leukemia Cells, Journal of Natural Products, 81, 1, 34-40, 2018.01, Harringtonine (HT) is a naturally occurring alkaloid isolated from the plant genus Cephalotaxus. It possesses antileukemic activity and has been clinically utilized for the treatment of acute leukemia and lymphoma. Sodium periodate (NaIO4) was reacted with HT to produce five HT derivatives including four novel compounds. Their antiproliferative activity against HL-60 acute promyelocytic leukemia cells revealed that the presence of the C-5′ methyl group enhances the antiproliferative activity because the IC50 values of the HT derivatives, including HT1 (5′-de-O-methylharringtonine), was at least 2,000 times higher (> 100 μM) than that of HT (~47 nM). In addition, an indirect competitive enzyme-linked immunosorbent assay (icELISA) using a monoclonal antibody against HT (MAb 1D2) revealed that these antiproliferative activities were related to their cellular uptake. These results indicated that esterification of HT1 at the C-4′ carboxylic acid group may enhance the antiproliferative activity of HT..
14.	Paudel, MK., Sakamoto, S., Tanaka, H., Morimoto, S., An overview and comparison of a recombinant antigen-binding fragment and an antigen-binding fragment from a monoclonal antibody against wogonin glucuronide, Journal of Natural Medicines, 71, 4, 703-710, 2017.10.
15.	Sakamoto S, Nagamitsu R, Yusakul G, Tomofumi M, Hiroyuki Tanaka, Morimoto S, Ultrasensitive immunoassay for monocrotaline using monoclonal antibody produced by N, N'-carbonyldiimidazole mediated hapten-carrier protein conjugates, Talanta, 168, 67-72, 2017.06.
16.	Paudel M, Sakamoto S, Huy LV, Hiroyuki Tanaka, Miyamoto T, Morimoto S, The effect of varying the peptide linker length in a single chain variable fragment antibody against wogonin glucuronide, Journal of Biotechnology, 251, 47-52, 2017.06.
17.	Sakamoto S, Yusakul G, Tsuneura Y, Putalun W, Usui K, Miyamoto T, Tanaka H, Morimoto S, Sodium periodate-mediated conjugation of harringtonine enabling the production of a highly specific monoclonal antibody, and the development of a sensitive quantitative analysis method, Analyst, 142, 1140-1148, 2017.04.
18.	Sakamoto S., Yusakul G., Nuntawong P., Kitisripanya T., Putalun W., Miyamoto T., Tanaka H., Morimoto S, Development of an indirect competitive immunochromatographic strip test for rapid detection and determination of anticancer drug, harringtonine, J. Chromatgr. B, 1048, 150-154, 2017.03.
19.	Paudel M, Sakamoto S, Huy LV, Hiroyuki Tanaka, Miyamoto T, Takano A, Morimoto S, Development of an immunoassay using an anti-wogonin glucuronide monoclonal antibody, J. Immunoassay Immunochem., 38, 2017.02.
20.	Taura　F, Iijima　M, Yamanaka E, Takahashi H, Saeki H, Morimoto S, Asakawa Y, Kurosaki　F, Morita　H, A novel class of plant type III polyketide synthase involved in orsellinic acid biosynthesis from Rhododendron dauricum, Frontiers in Plant Science, 7, 記事番号1452, 2016.09.
21.	Yusakul G., Sakamoto　S, Pongkitwitoon B, Tanaka H, Morimoto S, Effect of linker length between variable domains of single chain variable fragment antibody against daidzin on its reactivity, Biosci. Biotechnol. Biochem., 80, 1306-1312, 2016.07.
22.	Yusakul G, Sakamoto　S, Tanaka H, Morimoto S, Efficient expression of single chain variable fragment antibody against paclitaxel using Bombyx mori nucleopolyhedrovirus bacmid DNA system and its characterizations, J. Nat. Med., 70, 3, 592-601, 2016.07.
23.	Sakamoto　S, Kohno T, kuniyoshi shimizu, Tanaka H, Morimoto S, Detection of ganoderic acid A in Ganoderma lingzhi by an indirect competitive enzyme-linked immunosorbent assay, Planta Medica, 82, 747-751, 2016.05.
24.	Sakamoto　S, Yusakul G, Pongkitwitoon B, Tanaka H, Morimoto S, Colloidal gold-based indirect competitive immunochromatographicassay for rapid detection of bioactive isoflavone glycosides daidzin andgenistin in soy products, Food Chem., 194, 191-195, 2016.03.
25.	Yusakul G, Morimoto S, Juengwatanatrakul T, Putalun W, Tanaka H, Sakamoto　S, Preparation and application of a monoclonal antibody against the isoflavone glycoside daidzin using a Mannich reaction-derived hapten conjugate, Phytochem. Anal., 27, 81-85, 2016.01.
26.	Sakamoto　S, Nagamitsu　R, Matsuura Y, Tsuneura Y, Kurose　H, Tanaka H, Morimoto S, A new approach of indirect enzyme-linked immunosorbent assay for determination of D-glutamic acid through in situ conjugation, Journal of Immunoassay and Immunochemistry, in press, 2016.01.
27.	Yusakul G, Udomsin O, Morimoto S, Tanaka H, Juengwatanatrakul T, Putalun W, Enzyme-linked immunosorbent assay by enhanced chemiluminescence detection for the standardization of estrogenic miroestrol in Pueraria candollei Graham ex Benth, Luminescence, 30, 568-575, 2015.08.
28.	Seiichi Sakamoto, Yusakul G., Pongkitwitoon B, Paudel, M.K., Hiroyuki Tanaka, Satoshi Morimoto, “Simultaneous determination of soy isoflavone glycosides, daidzin and genistin by monoclonal antibody-based highly sensitive indirect competitive enzyme-linked immunosorbent assay, Food. Chem., 169, 127-133, 2015.01.
29.	Limsuwanchote S, Wungsintaweekul J, Yusakul G, Han J.Y., Kaori Tabata, Hiroyuki Tanaka, Yukihiro Shoyama, Satoshi Morimoto, Preparation of a monoclonal antibody against notoginsenoside R1, a distinctive saponin fromPanax notoginseng, and its application to indirect competitive ELISA, Planta Med, 80, 4, 337-342, 2014.04.
30.	Madan Kumar Paudel, Osamu Shirota, Kaori Tabata, Hiroyuki Tanaka, Setsuko Sekita, Satoshi Morimoto, Development of an enzyme immunoassay using a monoclonal antibody against the psychoactive diterpenoid salvinorin A, J.Nat. Prod, 10.1021/np400358n, 76, 9, 1654-1660, 2013.09, Salvinorin A (1), the main active constituent in Salvia divinorum, is a highly selective kappa-opioid receptor agonist with hallucinogenic effects, which is regulated in several countries. In the present study, a monoclonal antibody (mAb) against 1 was prepared, and an indirect competitive enzyme-linked immunosorbent assay (icELISA) system was developed for the detection of salvinorins. To raise mAbs against 1, salvinorin B (2) hemisuccinate was synthesized and used to prepare the immunogen 2-bovine serum albumin conjugate. This technique was used to prepare a hybridoma cell line, 3D5, which secreted a rnAb that recognized 1. The mAb was shown to have specificity for 1 and other salvinorins in cross-reactivity tests. The intra-assay calibration range by icELISA using the mAb against 1 was 0.0195-0.625 mu g/mL. After validating the icELISA using intra- and interassays, a recovery experiment and analysis of several plants in the family Lamiaceae, including S. divinorum, confirmed that the analytical method based on ELISA is not only simple but also precise, accurate, sensitive, and sufficiently reliable. The results indicate that icELISA is a useful tool in the identification of S. divinorum..
31.	Tanaka H., Paudel M., Juengwatanatrakul T., Sasaki-Tabata K., Waraporn P., De-Eknamkul W., Matangkasombut O., Shoyama Y., Morimoto, S., Fluobodies against Bioactive Natural Product and Its Application in Fluorescence-Linked Immunosorbent Assay , Antibodies, in press, 2012.10, Immunochemical Analysis of Anti-malarial Drugs, Artemisinin and Artesunate.
32.	Yoshinari Shoyama, Taro Tamada, Kazuo Kurihara, Ayako Takeuchi, Futoshi Taura, Shigeki Arai, Blaber Michael, Yukihiro Shoyama, Satoshi Morimoto, Ryota Kuroki, Ph.D. , Tetrahydrocannabinolic Acid (THCA) Synthase, the Enzyme Controlling the Psychoactivity of Cannabis sativa , Journal of Molecular Biology, 423, 96-105, 2012.10, ∆1-Tetrahydrocannabinolic acid (THCA) synthase catalyzes the oxidative cyclization of cannabigerolic acid (CBGA) into THCA, the precursor of the primary psychoactive agent ∆1-tetrahydrocannabinol in Cannabis sativa. In order to investigate the structure-function relationship of THCA synthase, the enzyme was over-produced in insect cells, purified, crystallized, and the tertiary structure determined to 2.75 Å resolution by X-ray crystallography (Rcryst=19.9%). The THCA synthase enzyme is a member of the p-cresol methyl-hydroxylase superfamily, and the tertiary structure is divided into two domains (domains I and II), with a flavin adenine dinucleotide (FAD) coenzyme positioned between each domain and covalently bound to His114 and Cys176 (located in domain I). The ionized residues in the active site of THCA synthase were investigated by mutational analysis and X-ray structure. The catalysis of THCA synthesis involves a hydride transfer from C3 of CBGA to N5 of flavin adenine dinucleotide (FAD) and the deprotonation of O6’ of CBGA. Mutation analysis indicates that the reaction does not involve the carboxyl group of Glu442 that was identified as the catalytic base in the related Berberine Bridge enzyme (BBE), but instead involves the hydroxyl group of Tyr484. Mutations at the active site residues His292 and Tyr417 resulted in a decrease in, but not elimination of, the enzymatic activity of THCA synthase, suggesting a key role for these residues in substrate binding and not direct catalysis. .
33.	Sakamoto S, Pongkitwitoon B, Nakahara H, Shibata O, Shoyama Y, Tanaka H, Morimoto S , Fluobodies against Bioactive Natural Product and Its Application in Fluorescence-Linked Immunosorbent Assay , Antibodies, 1, 239-258, 2012.09, Abstract: An enzyme-linked immunosorbent assay (ELISA) using monoclonal antibody (MAb), Fab antibody, and single-chain variable fragment (scFv) antibody have become one of the promising analytical methods owing to its rapidity, sensitivity, and reliability. Recently, a chimera of green fluorescent protein (GFP) with a scFv antibody, named fluobody, has been proposed as a probe for an alternative immunosorbent assay; i.e., fluorescence-linked immunosorbent assay (FLISA). In this FLISA, even more sensitive, simple, and rapid immunoassay can be performed by detecting highly sensitive fluorophore of GFP that is genetically and directly fused to scFv antibody. In addition, time- and cost-consuming secondary antibody reaction and following enzyme-substrate reaction necessary for conventional ELISA can be avoided, making it possible to complete the assay more rapid. Focusing on naturally occurring bioactive product, fluobody recognizing 1,4-naphthoquinone, plumbagin and triterpenoid saponin, ginsenosides was successfully expressed in Escherichia coli (E. coli) and applied them to FLISA. The construction, expression, and the potential use of fluobody in quantitative/qualitative analysis of bioactive natural product have been reviewed in this article. .
34.	Sritularak, B, Juengwatanatrakul, T, Putalun, W, Tanaka, H, Morimoto, S , A rapid one-step immunochromatographic assay for the detection of asiaticoside, Journal of Natural Medicines, 10.1007/s11418-011-0582-2, 78, 11, 1287-1288, 2012.04, Asiaticoside has been identified as the most active compound in Centella asiatica. In order to screen a large number of plant samples for the presence of asiaticoside, a rapid and simple technique is required that utilizes small quantities for test samples. In this study, an immunochromatographic strip test has been developed for the detection of asiaticoside in plant samples that uses a monoclonal antibody against asiaticoside. The limit of detection for the strip test was 12.5 mu g/ml. Immunoassay using monoclonal antibodies could be useful for the determination of small quantities of asiaticoside in plant extracts. .
35.	Paudel M.K., Putalun W., Sritularak B, Morinaga, O., Shoyama Y., Tanaka H. and Morimoto S., Development pf a combined technique using a rapid one-step immunochromatographic assay and indirect competitive ELISA for the rapid detection of bacalin, Analytica Chimica Acta, 10.1016/j.aca.2011.05.054 , 701, 2, 189-193, 701, (2) 189-193, 2012.02, A colloidal gold conjugated anti-baicalin monoclonal antibody (anti-BA MAb) was prepared and used in an immunochromatographic assay (ICA) for BA in Scutellariae Radix and Kampo medicines. This competitive ICA uses an anti-BA MAb which shows a high specificity for BA and baicalein. Its advantages include a short assay time (15 min), no dependence on any instrumental systems, and it can detect BA in plant materials and Kampo medicines. The limit of detection for the ICA was found to be around 0.6 mu g mL(-1) of baicalin. Moreover, the usefulness of the combination of indirect competitive ELISA and the ICA using anti-BA MAb as a quality control method was confirmed for analysis of BA in Scutellariae Radix and Kampo medicines with a sufficient sensitivity (200 ng mL(-1) to 2 mu g mL(-1)), obtainable in an easy and timely manner. .
36.	Madan K Paudel, Ayako Takei, Junichi Sakoda, Juengwatanatrakul, Thaweesak, Kaori Tabata, Putalun Waraporn, Shoyama Yukihiro, Hiroyuki Tanaka, Satoshi Mrimoto, Preparation of a single-chain variable fragment and a recombinant antigen-binding fragment against the anti-malarial drugs, artemisinin and artesunate, and their application in an ELISA, Analytical Chemitry, 10.1021/ac203131f, 701, 2, 2002-2008, 2012.02, Two different recombinant antibodies, a single-chain variable fragment (scFv) and an antigen-binding fragment (Fab), were prepared against artemisinin (AM) and artesunate (AS) and were developed for use in an enzyme-linked immunosorbent assay (ELISA). The recombinant antibodies, which were derived from a single monoclonal antibody against AM and AS (mAb 1C1) prepared by us, were expressed by Escherichia coli cells and their reactivity and specificity were characterized. As a result, to obtain sufficient signal in indirect ELISA, a much greater amount of a first antibody was needed in the use of scFv due to the differences of the secondary antibody and conformational stability. Therefore, we focused on the development of the recombinant Fab antibodies and applied it to indirect competitive ELISA. The specificity of the Fab was similar to that of mAb 1C1 in that it showed specific reactivity toward AM and AS only. The sensitivity of the icELISA (0.16 mu g/mL to 40 mu g/mL for AM and 8.0 ng/mL to 60 ng/mL for AS) was sufficient for analysis of antimalarial drugs, and its utility for quality control of analysis of Artemisia spp. was validated. The Fab expression and refolding systems provided a good yield of high-quality antibodies. The recombinant antibody against AM and AS provides an essential component of an economically attractive immunoassay and will be useful in other immunochemical applications for the analysis and purification of antimalarial drugs.iae Radix and Kampo medicines with a sufficient sensitivity (200 ng mL(-1) to 2 mu g mL(-1)), obtainable in an easy and timely manner. .
37.	Sakamoto, S., Putalun, W., Pongkitwitoon, B., Shoyama, Y., Tanaka, H., Morimoto, S., Modulation of plumbagin production in Plumbago zeylanica using a single-chain variable fragment antibody against plumbagin, Plant Cell Reports, 10.1007/s00299-011-1143-6, 31, 1, 103-110, 2012.01, A single-chain variable fragment antibody (scFv) against plumbagin (PL) accumulated the PL production in the hairy roots of Plumbago zeylanica. Recombinant Agrobacterium rhizogenes (ATCC 15834) containing an scFv gene against PL (PL-scFv) were obtained through triparental mating and transformed into P. zeylanica to induce PL-scFv protein in the hairy roots. Up to 40 mu g recombinant PL-scFv were expressed per milligram of soluble protein in transgenic P. zeylanica hairy root cultures. The mean PL content obtained from transgenic hairy roots (12.24 mu g/100 mg dry weight) exhibited 2.2 times higher than those obtained from wild-type (5.48 mu g/100 mg dry weight). The high correlation between the PL-scFv expression level and PL content of the recombinant plants suggested that the PL biosynthesis pathway had been modulated by the expression of PL-scFv protein in the hairy roots of P. zeylanica. .
38.	Sakamoto, S., Pongkitwitoon, B., Sasaki-Tabata, K., Putalun, W., Maenaka, K., Tanaka, H., Morimoto, S. , A fluorescent single domain antibody against plumbagin expressed in silkworm larvae for fluorescence-linked immunosorbent assay (FLISA) , Analyst, 10.1039/c1an15027h , 136, 10, 2056-2063, 136 (10) 2056-2063, 2011.10.
39.	Motosuke Hirunuma, Yoshinari Shoyama, Kaori Sasaki, Seiichi Sakamoto, Futoshi Taura, Yukihiro Shoyama, Hiroyuki Tanaka and Satoshi Morimoto, Flavone-catalyzed apoptosis in Scutellaria baicalensis, Phytochemistry, 10.1016/j.phytochem.2011.02.009 , 72, 8, 752-760, 72 (8) 752-760, 2011.06.
40.	Sakamoto, S., Pongkitwitoon, B., Nakamura, S., Sasaki-Tabata, K., Tanizaki, Y., Maenaka, K. Tanaka, H., Morimoto, S. , Construction, expression, and characterization of a single-chain variable fragment antibody against 2, 4- dichlorophenoxyacetic acid in the hemolymph of silkworm larvae, Appl. Biochem. Biotechnol., 10.1007/s12010-011-9168-4 , 164, 6, 715-728, 164 (6) 715-728, 2011.06.
41.	Sakamoto, S., Tanizaki, Y., Pongkitwitoon, B., Tanaka, H., Morimoto, S., A chimera of green fluorescent protein with single chain variable fragment antibody against ginsenosides for fluorescence-linked immunosorbent assay , Protein Expression and Purification, 10.1016/j.pep.2011.01.010 , 77, 1, 124-130 , 77 (1) 124-130, 2011.05.
42.	Juengwatanatraku, T., Sritularak, B., Amornnopparattanakul, P.,Tassanawat, P.,Putalun, W., Tanaka, H., Morimoto, S. , Preparation of a specific monoclonal antibody to asiaticoside for the development of an enzyme-linked immunosorbent assay , Analyst, 10.1039/c0an00868k , 136, 5, 1013-1017, 136 (5) 1013-1017, 2011.05.
43.	B. Pongkitwitoon, S. Sakamoto, O. Morinaga, T. Juengwatanatrakul, Y. Shoyama, H. Tanaka, S. Morimoto., Single-chain variable fragment antibody against ginsenoside Re as an effective tool for the determination of ginsenosides in various ginsengs, J. Nat. Med., 10.1007/s11418-010-0446-1 , 65, 1, 24-30, 65 (1) 24-30, 2011.01.
44.	S. Sakamoto, F. Taura, R. Tsuchihashi, W. Putalun, J. Kinjo, H. Tanaka, S. Morimoto, Expression, purification and characterization of anti-plumbagin single-chain variable fragment antibody in Sf9 insect cell, Hybridoma, 10.1089/hyb.2010.0052 , 29, 6, 481-488 , 29 (6) 481-488, 2010.12.
45.	S. Sakamoto, B. Pongkitwitoon, S. Nakamura, K. Maenaka, H. Tanaka, S. Morimoto, Efficient silkworm expression of single-chain variable fragment antibody against ginsenoside Re using Bombyx mori nucleopolyhedrovirus bacmid DNA system and its application in enzyme-linked immunosorbent assay for quality control of total ginsenosides”, Journal of Biochemistry, 10.1093/jb/mvq072 , 148, 3, 335-340 , 148 (3) 335-340 , 2010.09.
46.	S. Sakamoto, F. Taura, B. Pongkitwitoon, W. Putalun, R. Tsuchihashi, J. Kinjo, H. Tanaka, S. Morimoto. , Development of sensitivity-improved fluorescence-linked immunosorbent assay using a fluorescent single domain antibody against bioactive naphthoquinone, plumbagin, Anal. Bioanal. Chem., 10.1007/s00216-010-3535-9 , 396, 8, 2955-2963, 396 (8) 2955-2963, 2010.04.
47.	F.Taura, S. Tanaka, C. Taguchi, T. Fukamizu, H. Tanaka, Y. Shoyama and S. Morimoto, Characterization of olivetol synthase, a polyketide synthase putatively involved in cannabinoid biosynthetic pathway, FEBS Letters, 10.1016/j.febslet.2009.05.024 , 583, 12, 2061-2066, 583 (12) 2061-2066, 2009.06.
48.	Yoshinari Shoyama, Chitomi Sugawa, Hiroyuki Tanaka, Satoshi Morimoto, Cannabinoids act as necrosis-inducing factors in Cannabis sativa, Plant Signaling & Behavior, 3, 12, 1111-1112, 3 (12) 1111-1112, 2008.12.
49.	Chiho Taguchi, Futoshi Taura, Taro Tamada, Yoshinari Shoyama, Yukihiro Shoyama, Hiroyuki Tanaka, Ryota Kuroki and Satoshi Morimoto, Crystallization and preliminary X-ray diffraction studies of polyketide synthase-1 (PKS-1) from Cannabis sativa, Acta Cryst. F, 10.1107/S1744309108003795 , f64, 3, 217-220, F64 (3) 217-220, 2008.02.
50.	F.Taura, E. Dono, S. Sirikantaramas, K. Yoshimura, Y. Shoyama, and S. Morimoto, Production of THCA by the biosynthetic enzyme secreted from transgenic Pichia pastoris, Biochem. Biophys. Res. Commun. , 10.1016/j.bbrc.2007.07.079, 361, 3, 675-680, 361(3) 675-680 , 2007.09.
51.	S. Morimoto, Y.Tanaka, K.Sasaki, H. Tanaka, T. Fukamizu, Y. Shoyama, Y. Shoyama and F.Taura, Identification and characterization of cannabinoids that induce cell death through mitochondrial permeablity transition in Cannabis leaf cells, J. Biol. Chem., 10.1074/jbc.M700133200 , 282, 28, 20739-20751 , 282 (28) 20739-20751, 2007.07.
52.	Sirikantaramas S, Morimoto S, Shoyama Y, Ishikawa Y, Wada Y, Shoyama Y, Taura F, The gene controlling marijuana psychoactivity molecular cloning and heterologous expression of D1-THCA from Cannabis sativa, J. Biol. Chem., 10.1074/jbc.M403693200, 279, 38, 39767-39774, 279 (38): 39767-39774 SEP 17 2004, 2004.09.

主要総説, 論評, 解説, 書評, 報告書等

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1.	Sakamoto S., Putalun W., Vimolmangkang S., Phoolcharoen W., Shoyama Y., Hiroyuki Tanaka, Morimoto S., Enzyme‑linked immunosorbent assay for the quantitative/qualitative analysis of plant secondary metabolites, Journal of Natural Medicines, 2017.11.
2.	Satoshi Mrimoto, Yukihiro Shoyama, Hiroyuki Tanaka, Seiichi Sakamoto, Application of Green Fluorescent Protein in Immunoassays , Advances in Bioscience and Biotechnology, 2014.01.
3.	森元　聡, カンナビノイドの植物生理学的研究　ネクローシス誘導因子として機能する大麻幻覚成分, ファルマシア, 2010.04.
4.	森元　聡, 生薬成分の生体防御　生薬成分の植物生体防御とのかかわり　－オウゴンについて, 臨床検査, 2009.08.
5.	森元　聡, 大麻幻覚成分の生合成に関する研究, ATIニュース　（財団法人新世代研究所）, 2009.01.
6.	森元　聡, 大麻の幻覚活性を制御する酵素, 酵素工学ニュース, 2008.04.

主要学会発表等

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1.	小松頌平, 坂元政一, Gorawit Yusakul, Warapon Putalun, 田中宏幸, 森元聡, Cephalotaxus属由来ハリントニンの一本鎖抗体の作製及びその応用研究, 日本生薬学会第6４回年会, 2017.09.
2.	和田伸司, 坂元政一, 田中宏幸, 森元聡, 苦味配糖体アマロゲンチンに対する迅速分析法の開発, 日本生薬学会第6４回年会, 2017.09.
3.	Sakamoto S, Nuntawong P, Yusakul G, Ratnatilaka N, Bhuket P, Kohno T, Kikkawa N, Rojsitthisak P, Shimizu K, Hiroyuki Tanaka, Morimoto S, The expression of anti-ganoderic acid A single chain variable fragment antibody using Escherichia coli expression systems and their reactivity THE JSPS-NRCT FOLLOW-UP SEMINAR 2017 AND 33RD INTERNATIONAL ANNUAL MEETING IN PHARMACEUTICAL SCIENCES (JSPS-NRCT 2017 AND IAMPS 33), Bangkok, Thailand, March 2-3, 2017 (poster) PP-2, HE JSPS-NRCT FOLLOW-UP SEMINAR 2017 AND 33RD INTERNATIONAL ANNUAL MEETING IN PHARMACEUTICAL SCIENCES (JSPS-NRCT 2017 AND IAMPS 33), 2017.03.
4.	橘川奈生, 坂元政一, 河野俊享, 清水邦義, 田中宏幸, 森元聡, 抗ganoderic acid Aモノクローナル抗体を用いた免疫クロマトグラフィーの確立,, 日本生薬学会第63回年会, 2016.09.
5.	坂元政一, Gorawit Yusakul, 長光梨花, 常浦裕未, Warapon Putalun, 宮本智文, 田中宏幸, 森元聡, セファロタキサス属アルカロイド、ハリントニンの高感度免疫定量法の確立, 日本生薬学会第63回年会, 2016.09.
6.	S Sakamoto, R Yusakul　, R Nagamitsu, Y Tsuneura, W Putalun, Tomofumi Miyamoto, H Tanaka, S Morimoto, Development of highly sensitive immunological techniques for determination of cephalotaxus alkaloids, harringtonine, The 9th Joint Natural Products Conference 2016 in Copenhagen, 2016.07.
7.	S Komatsu, S Sakamoto, R Yusakul　, W Putalun, Tomofumi Miyamoto, H Tanaka, S Morimoto, A single-chain variable fragment antibody against anti-leukemia agent, harringtonine as a tool for immunomodulation, The 9th Joint Natural Products Conference 2016 in Copenhagen, 2016.07.
8.	G.Yusakul, Seiichi Sakamoto, T.Juengwatanatrakul, W.Putalun, Hiroyuki Tanaka, Satoshi Morimoto, Production and characterization of monoclonal antibodies against the isoflavone glycoside daidzein, The 4th Current Drug Development International Conference 2016, 2016.06.
9.	Kohno, T, Seiichi Sakamoto, Hiroyuki Tanaka, Satoshi Morimoto, Development of an indirect competitive enzyme-linked immunosorbent assay (icELISA) using highly specific monoclonal antibody against ganoderic acid A, The 1st International Conference on Herbal and Traditional Medicine , 2015.01.
10.	Yusakul G, Seiichi Sakamoto, Hiroyuki Tanaka, Satoshi Morimoto, Construction and characterization of the antigen-binding antibody fragment against paclitaxel”, The 1st International Conference on Herbal and Traditional Medicine , 2015.01.
11.	中島　由貴, 坂元政一, 田中　宏幸, 森元　聡, 植物アポトーシスにおけるシロイヌナズナ由来Cytochromecの機能解析, 日本生薬学会第61回年会, 2014.09.
12.	堀　太樹, 坂元政一, 田中　宏幸, 森元　聡, ケシ由来パーオキシダーゼの機能解析, 日本生薬学会第61回年会, 2014.09.
13.	加藤　梨那, 中村　俊介, 相星　彩佳, 坂元　政一, 田中　宏幸, 森元　聡, 植物ネクローシスにおけるcyclophilin Dの機能解析と抗体作製”, 日本生薬学会第61回年会, 2014.09.
14.	Seiichi Sakamoto, Putalun W., Hiroyuki Tanaka, Satoshi Morimoto, Enhanced plumbagin production in hairy root culture of Plumbago zeylanica by anti-plumbagin single-chain fragment antibody, The 8th JSP-CCTCNM-KSP Joint Symposium on Pharmacognosy, 2014.09.
15.	Khono T, Bang T.H., kuniyoshi shimizu, Seiichi Sakamoto, Hiroyuki Tanaka, Satoshi Morimoto, Tubulin-polymerizing activity of Ganoderma triterpenoids and production of their monoclonal antibody, The 8th JSP-CCTCNM-KSP Joint Symposium on Pharmacognosy, 2014.09.
16.	Paudel M.K., Seiichi Sakamoto, Hiroyuki Tanaka, Satoshi Morimoto, Development of an immunoassay using anti-wogonin glucuronide monoclonal antibody, The 8th JSP-CCTCNM-KSP Joint Symposium on Pharmacognosy, 2014.09.
17.	加藤梨那, 中村俊介, 相星彩佳, 坂元政一, 田畑香織, 田中宏幸, 森元聡, 植物ネクローシスにおけるcyclophilinDの機能解析, 日本薬学会第134年会, 2014.03.
18.	常浦裕未, 田畑香織, 坂元政一, 田中宏幸, 麻生真理子, 末宗洋, 森元聡, 新規D-アミノ酸分析開発法を目指した抗D-セリンモノクローナル抗体の作成, 日本薬学会第134年会, 2014.03.
19.	加藤梨那, 田中宏幸, 森元聡, 田畑香織, 植物ネクローシスにおけるcyclophilinDの機能解析, 日本生薬学会　第60回年会, 2013.09.
20.	戸切祥恵, 田中宏幸, 森元聡, 田畑香織, ケシにおけるモルヒネ代謝酵素に関する研究, 日本生薬学会　第60回年会, 2013.09.
21.	ポウデルマダンクマル、田中宏幸、田畑香織、森元聡、代田修、関田節子, 免疫化学的手法によるチャット鑑別法の開発, 日本生薬学会　第５９回年会, 2012.09.
22.	田中宏幸、相星彩香、田畑香織、森元　聡、畠中孝彰、伊東祐二, THCA誘導性植物ネクローシスに関する研究, 日本生薬学会　第５９回年会, 2012.09.
23.	Tanaka, H, Paudel, MK, Takei, A, Sakoda, J, Juengwatanatrakul, T, Sasaki-Tabata, K, Putalun, W, Shoyama, Y, Morimoto, S , Preparation of a reconbinant fab against the anti-malarial drugs, artemisinin and artesunate and their application in an ELISA , International Congress on Natural Products Research on Global Change, Natural Products and Human Health/8th Joint Meeting of AFERP, 2012.07.
24.	Paudel M, Shirota O, Sekita S, Tanaka H, Morimoto s, Development of an immunochemical differentiation method for Salvia divinorum, International Congress on Natural Products Research, 2012.07.
25.	Benyakan Pongkitwitoon, Seiichi Sakamoto, Kaori Sasaki, Hiroyuki Tanaka, Satoshi Morimoto, Molecular cloning and expression of O-methyltransferases from opium poppy, PHYTOPHARM 2012, 2012.07, [URL], ackground: Papaver somniferum (opium poppy) has been known to be the essential source for several pharmaceutically important benzylisoquinoline alkaloids (BIAs) such as morphine, codeine, sanguinarine and papaverine. O-Methylation is regarded as an important reaction step in BIAs biosynthesis. Several cDNAs encoding proteins that catalyze these reactions have been reported, whereas many steps are still unclear. In this study, we attempt to clone P.somniferum O-methyltransferases to better understand biosynthetic pathways of BIAs in this plant. Methods: cDNA fragments encoding O-methyltransferase were amplified by homology-based RT-PCR using degenerate primers designed from conserved sequences of reported P.somniferum O-methyltransferases. 3’- and 5’- end regions of cDNAs were obtained by rapid amplifications of cDNA ends. The full length cDNAs were then engineered to be expressed in silkworm using a rapid Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid DNA system. Results and discussions: Four cDNAs encoding polypeptides named PSOMT1, PSOMT2, PSOMT3, and PSOMT4, which consist 355, 356, 354, and 358 amino acids respectively, were cloned. Conserved motifs including SAM binding region, catalytic histidine, and metal binding region were found. The cloned cDNAs encoding these peptides are successfully expressed in the hemolymph of silkworm larvae. The purified PSOMTs are to be characterized as further study. .
26.	清水瑠美, 安達基泰, 黒木良太, 山下未知, 森元聡, モルヒネの代謝反応を触媒する組換え型パーオキシダーゼの調製, 日本蛋白質科学会, 2012.06.
27.	今村聡、今村麻美、坂元政一、田畑香織、田中宏幸、森元聡, コガネバナβ-glucuronidaseの反応メカニズムに関する研究, 日本薬学会第１３２年会, 2012.03, 【目的】黄ごんの基原植物であるコガネバナは古くからバイカリンと称されるフラボン配糖体を生産していることが知られている。併せてバイカリンは内在性のグルクロニダーゼ(sGUS)によって代謝されることも明らかにされている。当研究室ではsGUS の遺伝子クローニングを行い、その一次構造を明確にしているが、本酵素の反応メカニズムに関しては、不明な点が多い。本研究では、sGUS の反応メカニズムを解明することを目的とする。【方法、結果】sGUS のTyr281 をPhe281 に変えた変異体を作製したところ、活性が大幅に低下したことから、本アミノ酸残基は活性に大きく関与することが判明した。そこで、Tyr281 の役割も含めsGUS の反応メカニズムを明確にするために、X 線結晶構造解析に向けたsGUS の大量発現系の確立及び結晶条件の検討を行った。大腸菌及びカイコを用いた系で発現した組換えsGUS を精製し、結晶条件を検討した。併せて、コガネバナカルスから抽出精製したsGUS も結晶化に使用した。この結果、カイコ由来のsGUS で結晶化がみられた。さらに、sGUS のモノクローナル抗体の作製を試みた結果、本酵素の活性を低下させる中和抗体の調整に成功した。現在、酵素抗体複合体の結晶化も検討している。【考察】sGUS の反応メカニズムに関してはGlu212 及びGlu329 がそれぞれacid/base catalyst 及びnucleophile として機能することを明らかにしているが、Tyr281 に関しては不明である。しかしながら、Tyr281 のフェノール性水酸基を除くと活性が著しく低下することから、これらのアミノ酸残基の電離に関与している可能性が推察された。今後、結晶構造の解明によって、本仮説の証明を試みる計画である。.
28.	Benyakan PONGKITWITOON，坂元　政一，佐々木　香織，田中　宏幸，森元　聡, ケシ由来O-Methyltransferase の遺伝子クローニングと発現, 日本薬学会第１３２年会, 2012.03, 【Background】 Papaver somniferum (opium poppy) has been known to be the essential source for several pharmaceutically-important benzylisoquinoline alkaloids (BIAs) such as morphine, codeine, sanguinarine and papaverine. O-Methylation is regarded as a quite important reaction step in BIAs biosynthesis. Several cDNAs encoding proteins that catalyze these reactions have been reported, whereas many steps are still unclear. In this study, we attempt to clone P.somniferum O-methyltransferases to better understand biosynthetic pathways of BIAs in this plant. 【Methods】cDNA fragments encoding O-methyltransferase were amplified by homology-based RT-PCR using degenerate primers designed from conserved sequences of reported P.somniferum O-methyltransferases. 3’- and 5’- end regions of cDNAs were obtained by rapid amplifications of cDNA ends. The full length cDNAs were then engineered to be expressed in silkworm using a rapid Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid DNA system. 【Results and discussions】Four cDNAs encoding polypeptides named PSOMT1, PSOMT2, PSOMT3, and PSOMT4, which consist 355, 356, 354, and 358 amino acids respectively, were cloned. Conserved motifs including SAM binding region, catalytic histidine, and metal binding region were found. The cloned cDNAs encoding these peptides are successfully expressed in the hemolymph of silkworm larvae. The purified PSOMTs are to be characterized as further study..
29.	峰　真也，田畑　香織，田中　宏幸，森元　聡, カンナビノイドの生育阻害の機能解明, 日本薬学会第１３２年会, 2012.03, 【目的】当研究室では、アサに含まれるカンナビノイドが、内在性の細胞死誘導因子として機能することを発見した。また、これらのカンナビノイドが他の植物にも細胞死を誘導し、生育を阻害することも明らかにしている。本研究では、カンナビノイドの生育阻害のメカニズムを明確にすることを目的とする。【方法・結果】シロイヌナズナ幼植物を各濃度のtetrahydrocannabinolic acid(THCA)溶液中で発芽を試みた結果、50μM 以上のTHCA 濃度で、根の生育阻害が認められた。そこで、根に対してfluorescein diacetate(FDA)染色を行ったところ、THCA 処理によって根のviability が著しく低下することが判明した。また、 tetramethylrhodamine methyl ester(TMRM)染色を行った結果、THCA が根のミトコンドリアに傷害を誘導することも明らかとなった。これらの結果から、THCA はシロイヌナズナの根のステムセルにネクローシス様の障害を与える可能性が示唆された。そこで、根の生育に関与している遺伝子(XXXX)の発現を調べてみた。この結果、50μM 以上THCA 処理によって、本遺伝子の発現低下が観察された。【考察】本研究により、THCA がシロイヌナズナに対しても、アレロケミカルとして機能する可能性が示唆された。THCA は根のviability を低下させるとともに、根の生育に関与している3 種の遺伝子の発現を著しく低下させることも明らかとなった。これらの3 種の遺伝子は根のステムセルに発現していることから、THCA は本細胞に傷害を与えることによって、根の生育を阻害しているものと考えられる。.
30.	Madan Kumar Paudel, 田中宏幸、森元聡、代田修、　関田節子, Development　of immunoassays using anti-salvinorin A monoclonal antibody, 日本生薬学会　第５８回年会, 2011.09.
31.	Benyakan Pongkitwitoon, Seiichi Sakamoto, Osamu Morinaga, Thaweesak Juengwatanatrakul, Yukihiro Shoyama,Hiroyuki Tanaka, Satoshi Morimoto, ELISA for the determination of ginsenosides in various ginsengs using single-chain variable fragment antibody against ginsenoside Re, The 5th JSP-CCTNM-KSP Joint Symposium on Pharmacognosy, 2010.09.
32.	Seiichi Sakamoto, Futoshi Taura, Benyakan Pongkitwitoon, Waraporn Putalun, Ryota Tsuchihashi, Junei Kinjo, Hiroyuki Tanaka, Satoshi Morimoto, Fluobody against plumbagin and its application to novel fluorescence-linked immunosorbent assay , The 5th JSP-CCTNM-KSP Joint Symposium on Pharmacognosy, 2010.09.
33.	山中絵里子、田浦太志、森元聡, エゾムラサキツツジ由来ポリケタイド合成酵素のクローニングと機能解析, 第26回日本薬学会九州支部大会, 2009.12.
34.	高取秀行、田中宏幸、森元聡, アサ由来カンナビノイドによる細胞死誘導経路に関する研究, 第26回日本薬学会九州支部大会, 2009.12.
35.	出口恭平、田浦太志、森元聡, 部位特異的変異を導入したアサポリケタイド合成酵素に関する研究, 第26回日本薬学会九州支部大会, 2009.12.
36.	S. Sakamoto, F. Taura, W. Putalun, B. Pongkitwitoon, R. Tsuchihashi, J. Kinjo, H. Tanaka and S. Morimoto., Development of fluorescence-linked immunosorbent assay using a fusion protein of green fluorescent protein and single chain variable fragment antibody against bioactive naphthoquinone, plumbagin, Asian Symposium for Pharmaceutical Science in JSPS Asian Core Program., 2009.11.
37.	B. Pongkitwitoon, S. Sakamoto, H. Tanaka, R. Tsuchihashi, J Kinjo, S. Morimoto and W. Putalun, Determination of total isoflavonoids in Pueraria Candollei by enxyme-linked immunosorbent assay using anti-puerarin and anti-daidzin polyclonal antibodies, Asian Federation for Pharmaceutical Sciences 2009, 2009.10.
38.	森元　聡, カンナビノイドの生合成に関する化学的・生物学的研究, 日本薬学会, 2009.03.
39.	S. Sakamoto, J. Sakoda, O. Morinaga, W. Putalun, R. Tsuchihashi, S. Morimoto, J. Kinjo, H. Tanaka., Determination of vitamin K3 by an indirect competitive ELISA using monoclonal　antibodies against plumbagin, The 8th Joint Seminar (INNOVATIVE RESEARCH IN NATURAL PRODUCTS FOR SUSTAINABLE DEVELOPMENT), 2009.02.
40.	森元　聡, 大麻に関する研究, 第2回薬学研究フォーラムin東京, 2008.12.
41.	斉藤由希子、田浦太志、正山征洋、森元聡, 大麻成分の生合成酵素に関する研究, 日本生薬学会第５５回年会, 2008.09.
42.	蛭沼基祐、田浦太志、正山征洋、森元聡, コガネバナにおけるフラボノイドの生理的役割の解明, 日本生薬学会第５５回年会, 2008.09.
43.	洲河千宝、田浦太志、森元聡、正山征洋, CBDAによるアサの細胞死誘導に関する研究, 日本生薬学会第５５回年会, 2008.09.
44.	鷲尾知美、田浦太志、正山征洋、森元聡, 構造研究を目的としたカタラーゼ発現システムの確立, 日本生薬学会第５５回年会, 2008.09.
45.	横尾啓史、田浦太志、正山征洋、森元聡, クルミのアレロパシーに関する研究, 日本生薬学会第５５回年会, 2008.09.
46.	M. Hirunuma, F. Taura, Y. Shoyama, and S. Morimoto, Studies on the physiological role of flavonoid in Scutellaria baicalensis, 2008.06.
47.	森元　聡, カンナビノイドの生合成に関する研究, 植物化学シンポジウム, 2007.11.
48.	田浦太志、道野恵美、Supaart Sirikantaramas, 吉村浩司、正山征洋、森元　聡, Pichia pastorisで分泌発現した生合成酵素によるTHCAの生産, 日本生薬学会第54回年会, 2007.09.
49.	Y. Shoyama, T. Tamada, A. Takeuchi, F. Taura, Y. Shoyama, R. Kuroki, S. Morimoto., Crystal structure of Delta1-tetrahydrocannabinolic acid synthase from Cannabis sativa, 2nd International Symposium on Diffraction Structural Biology 2007 , 2007.09.
50.	森元　聡, 植物の細胞死に関る分子機構, 第2回生体中性子ナノマシン構造研究会, 2006.11.
51.	Satoshi Morimoto, Studies on Physiological Functions of Secondary Metabolites in Plants, 2006.10.

特許出願・取得

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所属学会名

日本植物細胞分子生物学会

日本生薬学会

日本薬学会

学協会役員等への就任

2018.03～2019.03, 日本生薬学会, 代議員.

2015.04～2016.03, 日本生薬学会関西支部, 支部委員.

2015.04～2016.03, 日本生薬学会, 代議員.

2015.04～2017.03, 日本薬学会, 代議員.

2014.04～2015.03, 日本生薬学会, 代議員.

2013.04～2014.03, 日本生薬学会, 評議員.

2013.04～2014.03, 日本薬学会　天然物部会, 世話人.

2013.04～2014.03, 日本生薬学会関西支部, 支部委員.

2012.04～2013.03, 日本薬学会　天然物部会, 世話人.

2012.04～2013.03, 日本生薬学会関西支部, 支部委員.

2012.04～2013.03, 日本生薬学会, 評議員.

2011.04～2012.03, 日本生薬学会, 評議員.

2011.04～2012.03, 日本生薬学会, 関西支部役員.

2010.04～2011.03, 日本生薬学会, 日本生薬学会表彰者選考委員.

2010.04～2011.03, 日本生薬学会, 評議員.

2009.09～2010.03, 日本薬学会, 日本薬学会学会賞第一次選考委員.

2009.04～2010.03, 日本生薬学会, 日本生薬学会表彰者選考委員.

2008.04～2010.03, 日本生薬学会, 評議員.

2008.01～2010.01, 日本薬学会九州支部, 幹事.

2008.04～2010.03, 日本生薬学会, 関西支部役員.

2006.04, 日本生薬学会, 関西支部役員.

学会大会・会議・シンポジウム等における役割

2010.12.11～2010.12.12, 第27回日本薬学会九州支部大会, 座長（Chairmanship）.

2009.10.03～2009.12.04, 日本生薬学会第56回年会, 座長（Chairmanship）.

2007.12.08～2007.12.09, 第24回日本薬学会九州支部, 座長（Chairmanship）.

2009.12.12～2009.12.13, 第26回日本薬学会九州支部大会, 座長（Chairmanship）.

2003.10, 生体中性子ナノマシン研究会, 研究委員.

2009.12.12～2009.12.13, 第２６回日本薬学会九州支部大会　, 準備委員長.

2008.09, 第５０回天然有機化合物討論会, 準備委員会委員.

2007.10, Asian Symposium forPharmaceutical Sciences in JSPS, Organizing Committee.

2006.01, Asian Symposium forPharmaceutical Sciences in JSPS, Organizing Committee.

2003.10, 日本生薬学会第４９回年会, 準備委員会副委員長.

学会誌・雑誌・著書の編集への参加状況

2008.01, 福岡医学雑誌, 国内, 編集幹事.

学術論文等の審査

年度	外国語雑誌査読論文数	日本語雑誌査読論文数	国際会議録査読論文数	国内会議録査読論文数	合計
2011年度	2	0	0	0	2
2010年度	3				3
2009年度	1				1
2008年度	2				0
2007年度	1				1
2003年度	5				5
2002年度	10				10
2001年度	5				5
1999年度	6				6

海外渡航状況, 海外での教育研究歴

北京大学, China, 2006.10～2006.10.

北京大学, China, 2006.03～2006.03.

カリフォルニア大学サンディエゴ校, UnitedStatesofAmerica, 1988.05～1989.09.

ジョンホプキンス大学, UnitedStatesofAmerica, 1987.06～1988.04.

外国人研究者等の受入れ状況

2015.03～2015.04, 1ヶ月以上, ナレスアン大学薬学部, Thailand, 学内資金.

2015.03～2015.04, コンケン大学, Thailand, 日本学術振興会.

2010.10～2010.11, 1ヶ月以上, チュラロンコン大学, Thailand, .

科学研究費補助金の採択状況(文部科学省、日本学術振興会)

2021年度～2023年度, 基盤研究(C), 代表, 大麻成分THCAによる根冠形成阻害の分子メカニズムの解明.

2018年度～2020年度, 基盤研究(C), 代表, 構造生物学を基盤としたマルバタバコのベルベリンブリッジ酵素様蛋白質の網羅的解析.

2016年度～2017年度, 挑戦的萌芽研究, 代表, 抗体工学を応用した有用薬用植物の作出研究.

2014年度～2015年度, 挑戦的萌芽研究, 代表, Fluorobody を用いた植物細胞死の網羅的解析.

2011年度～2013年度, 基盤研究(C), 代表, 薬用植物の活性酸素代謝機構に関する構造生物学的研究.

2008年度～2010年度, 基盤研究(C), 代表, 分子生物学・構造生物学を基盤とした植物ネクローシスに関する研究.

2002年度～2003年度, 基盤研究(C), 代表, モルヒネ高含有ケシの分子育種に向けたモルヒネの代謝研究.

2003年度～2005年度, 基盤研究(B), 分担, 樹木のリグニン生合成とストレス応答におけるペルオキシダーゼ機能と発現の解析.

2005年度～2005年度, 基盤研究(C), 分担, 生体高分子の機能発現における水素・水和水の静的・動的な役割の実証.

科学研究費補助金の採択状況(文部科学省、日本学術振興会以外)

2006年度～2006年度, 科学技術振興調整費, 分担, 機能性食品等の迅速な科学的評価法の開発.

競争的資金(受託研究を含む)の採択状況

2007年度～2007年度, ＳＰring-8利用研究課題(2007年度後期分）, 代表, 大麻ポリケタイド合成酵素の結晶構造解析 .

2007年度～2008年度, 高エネルギー加速器研究機構放射光共同研究課題, 代表, 大麻成分の生合成酵素の結晶構造解析.

2005年度～2005年度, ＳＰring-8利用研究課題(2005B期）, 代表, 大麻成分の生合成酵素の結晶構造解析.

2005年度～2005年度, 日本原子力研究所黎明研究, 代表, 大麻幻覚活物質を生合成する経路の構造化学的解明.

2004年度～2004年度, ＳＰring-8利用研究課題(2004B期）, 代表, 題大麻成分の生合成酵素の結晶構造解析.

共同研究、受託研究(競争的資金を除く)の受入状況

2011.04～2012.03, 代表, 薬用植物を活用した商品の開発研究.

2010.07～2011.03, 代表, 薬用植物を活用した商品の開発研究.

2009.05～2010.03, 代表, 薬用植物を活用した商品の開発研究.

寄附金の受入状況

2008年度, ﾋｭｳｶﾞﾄｳｷに関する研究.


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