ISHII Takahiro

写真a

Title

Professor

Researcher Number(JSPS Kakenhi)

70450393

Current Affiliation Organization 【 display / non-display

  • Duty   University of the Ryukyus   Faculty of Agriculture   Bioscience and Biotechnology   Professor  

  • Concurrently   University of the Ryukyus   Graduate School of Agriculture   Professor  

University 【 display / non-display

  • 1997.04
    -
    2001.03

    Nihon University   Faculty of Science and Engineering   Graduated

Graduate School 【 display / non-display

  • 2001.04
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    2003.03

    Hokkaido University  Graduate School, Division of Earth Environmental Science and Technology  Master's Course  Completed

  • 2003.04
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    2006.06

    Hokkaido University  Graduate School, Division of Earth Environmental Science and Technology  Doctor's Course  Completed

External Career 【 display / non-display

  • 2006.07
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    2008.03

     

  • 2006.08
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    2007.03

     

  • 2006.12
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    2007.03

     

  • 2007.04
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    2008.03

     

  • 2008.04
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    2008.05

     

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Research Interests 【 display / non-display

  • 天然物有機化学,生物活性物質学,水産化学, 農薬化学,創薬化学,化学生態学

Research Areas 【 display / non-display

  • Life Science / Bioorganic chemistry

  • Life Science / Environmental and natural pharmaceutical resources

  • Life Science / Aquatic life science

  • Environmental Science/Agriculture Science / Plant protection science

Acquisition of a qualification 【 display / non-display

  • Hazardous Material Handler (first kind)

Thesis 【 display / non-display

  • Studies on Bioactive Compounds from Unutilized Marine Natural Resources

    2006.06

Published Papers 【 display / non-display

  • Morphological and Chemical Diversity within Japanese Laurencia Complex (Rhodomelaceae, Ceramiales, Rhodophyta).

    Yamagishi Y, Kamada T, Ishii T, Matsuura H, Kikuchi N, Abe T, Suzuki M

    Chemistry & biodiversity ( Wiley )    e202400833   2024.07 [ Peer Review Accepted ]

    Type of publication: Research paper (scientific journal)

     View Summary

    Seaweeds of the red algal genus Laurencia are widely distributed worldwide in tropical, subtropical to temperate zones, and grow in Japan from Hokkaido to Okinawa. Laurencia is one of the most studied seaweeds by organic chemists because it produces a variety of compounds with unique structures. In Japan, various halogenated compounds have been found in Laurencia, while some species do not produce any halogenated compounds. Laurencia is one of the most difficult seaweeds to classify morphologically; however, the major halogenated secondary metabolites produced tend to be species‐specific, and these compounds can be used as chemical markers for chemical systematics (chemotaxonomy). Similarly, it has been confirmed that domestic Laurencia species produce species‐specific halogenated compounds of certain types. Laurencia is one of the "weedy seaweeds" that have not been effectively utilized at present, but it produces a wide variety of metabolites, so there is a good possibility that compounds with specific activity may be found. Thus, it can be seen that the secondary metabolites in Laurencia have many interesting aspects. In this review, we reported significant morphological features to distinguish species in this genus, and the morphological features, habitat, distribution, and chemical composition that help discriminate Japanese Laurencia species.

  • Halogenated Cyclic Monoterpenoids with Anti-biofouling Activity from the Okinawan Red Marine Algae Portieria hornemannii.

    Ishigami S, Fukada R, Nagasaka G, Tsuruta T, Nishikawa K, Sasaki Y, Nimura K, Oshima I, Yamagishi Y, Morimoto Y, Kamada T, Ishii T

    Chemistry & biodiversity     e202400436   2024.03 [ Peer Review Accepted ]

    Type of publication: Research paper (scientific journal)

  • A new analog of dihydroxybenzoic acid from Saccharopolyspora sp. KR21-0001.

    Janthanom R, Kikuchi Y, Kanto H, Hirose T, Tahara A, Ishii T, Thamchaipenet A, Inahashi Y

    Beilstein journal of organic chemistry ( Beilstein Journal of Organic Chemistry )  20   497 - 503   2024 [ Peer Review Accepted ]

    Type of publication: Research paper (scientific journal)

     View Summary

    Actinomycetes are well-known as the main producers of bioactive compounds such as antibiotics, anticancers, and immunosuppressants. Screening of natural products from actinomycetes has been an essential part of several drug discovery programs. Finding such novel biologically active metabolites is immensely important because of their beneficial health effects. Recently, the discovery of new compounds has diverted attention to rare actinomycetes, since they are rich sources of natural products. In this study, a collection of rare actinomycetes at Kitasato University has been screened for potential novel compound producers. Among the rare actinomycetes, Saccharopolyspora sp. KR21-0001 isolated from soil on Ōha Island, Okinawa, Japan was selected as a potential producer. The strain was cultured in 20 L of production medium in a jar fermenter and the culture broth was extracted. Further purification revealed the presence of a new compound designated KR21-0001A (1). The structure was elucidated by NMR, and the absolute stereochemistry was determined by advanced Marfey's method. The results indicated that 1 is a new analog of dihydroxybenzoic acid. 1 has no antimicrobial activity against bacteria and fungi but showed potent antioxidant activity.

  • Lemnalol acetate, ylangene-type sesquiterpenoid isolated as natural product from the soft coral genus Lemnalia collected in Okinawa

    5. Nakagawa, R., Miwa, T., Miyaji, T., Nakamura, R., Nimura, K., Fukada, R., Ishii, T., Hamada, T., Kamada, T.

    Galaxea     2024 [ Peer Review Accepted ]

    Type of publication: Research paper (scientific journal)

  • A novel aromatic compound from the fungus <i>Synnemellisia</i> sp. FKR-0921

    Tahara, A; Tani, K; Wakatsuki, M; Tokiwa, T; Higo, M; Nonaka, K; Hirose, T; Hokari, R; Ishiyama, A; Iwatsuki, M; Watanabe, Y; Honsho, M; Asami, Y; Matsui, H; Sunazuka, T; Hanaki, H; Teruya, T; Ishii, T

    JOURNAL OF ANTIBIOTICS ( Journal of Antibiotics )    2023.09 [ Peer Review Accepted ]

    Type of publication: Research paper (scientific journal)

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Other Papers 【 display / non-display

  • Search for antileishmanial compounds from microbial metabolites

    橋本瑞希, 村山諒, 渡邊善洋, 渡邊善洋, 肥後茉由佳, 肥後茉由佳, 野中健一, 野中健一, 稲橋佑起, 稲橋佑起, 石川春樹, 丑田公規, 石井貴広, 照屋俊明, 石山亜紀, 石山亜紀, 穗苅玲, 穗苅玲, 岩月正人, 岩月正人

    日本薬学会年会要旨集(Web)   143rd   2023

     

    J-GLOBAL

  • Corrigendum: Two New Halogenated Compounds from the Marine Red Alga Laurencia nipponica Yamada from the Kunashiri and Etorofu Islands.

    Kosuke Sato, Kensuke Kaneko, Tsuyoshi Kamekawa, Kanako Taba, Shinnosuke Ishigami, Masahiro Wada, Takahiro Ishii, Tsuyoshi Abe, Takashi Kamada, Minoru Suzuki

    Chemistry & biodiversity   19 ( 3 ) e202200112   2022.03

     

    DOI PubMed

  • Search for antimalarial compounds from microbial metabolites

    木村奏一朗, 渡邊善洋, 渡邊善洋, 小池李茉, 穗苅玲, 穗苅玲, 石山亜紀, 石山亜紀, 浅見行弘, 浅見行弘, 野中健一, 野中健一, 稲橋佑起, 稲橋佑起, 木村透, 照屋俊明, 石井貴広, 岩月正人, 岩月正人

    日本薬学会年会要旨集(Web)   142nd   2022

     

    J-GLOBAL

  • Search for therapeutic seeds for cutaneous leishmaniasis with mitochondrial function inhibitory activity using multidrug-sensitive Saccharomyces cerevisia

    山中綾乃, 穗苅玲, 穗苅玲, 村山諒, 荒川絵美, 渡邊善洋, 渡邊善洋, 石山亜紀, 石山亜紀, 本庄雅子, 浅見行弘, 浅見行弘, 野中健一, 野中健一, 肥後茉由佳, 肥後茉由佳, 村松怜子, 稲橋佑起, 稲橋佑起, 丑田公規, 照屋俊明, 石井貴広, 臼井健郎, 岩月正人, 岩月正人

    日本薬学会年会要旨集(Web)   142nd   2022

     

    J-GLOBAL

  • Corrigendum to: Auxin signaling through SCFTIR1/AFBs mediates feedback regulation of IAA biosynthesis.

    Shin Takato, Yusuke Kakei, Marie Mitsui, Yosuke Ishida, Masashi Suzuki, Chiaki Yamazaki, Ken-Ichiro Hayashi, Takahiro Ishii, Ayako Nakamura, Kazuo Soeno, Yukihisa Shimada

    Bioscience, Biotechnology, and Biochemistry   85 ( 6 ) 1562 - 1562   2021.05  [Refereed]

     

    DOI PubMed

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Presentations 【 display / non-display

  • マレーシア産軟体サンゴ由来の生物活性物質

    Phan Chin-Soon・鎌田昂・石井貴広・濱田季之・Vairappan Charles S.

    日本サンゴ礁学会第22回大会  (札幌)  2019.11  -  2019.11 

  • マレーシアサバ州に分布する軟質サンゴ由来の新規テルペンとその生物活性

    パンチンスン・鎌田昂・濱田季之・石井貴広・バイラパンチャールズ

    第63回香料・テルペンおよび精油化学に関する討論会  (秋田)  2019.09  -  2019.09 

  • Bioactive Terpenes from Soft Corals in North Borneo

    2018.10  -  2018.10 

  • Bioactive Terpenes from Soft Corals in North Borneo

    2018.10  -  2018.10 

  • Sex steroid as the possible key in oocyte development of the scleractinian coral, Acropora tenuis

    Tan, E., Izumi, R., Ishii, T., Takeuchi, Y., Yang, S., Shikina, S., Chang, C. F., Takemura, A.

    日本動物学会第89回大会  (札幌)  2018.09  -  2018.09 

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Industrial Property 【 display / non-display

  • no_title

    Industrial Property No no_data  (1900.01.01)

    Unexpectedly No no_data  (1900.01.01)

  • no_title

    Industrial Property No no_data  (1900.01.01)

    Unexpectedly No no_data  (1900.01.01)

Academic Awards 【 display / non-display

  • Silver award (Research and Innovation Competition (Pereka) UMS 2009)

    2009.07   Universiti Malaysia Sabah  

     View Summary

    Novel marine metabolites with potent pharmaceutical potentials

Grant-in-Aid for Scientific Research 【 display / non-display

  • Grant-in-Aid for Scientific Research(C)

    Project Year: 2022.04  -  2025.03 

    Direct: 3,200,000 (YEN)  Overheads: 4,160,000 (YEN)  Total: 960,000 (YEN)

  • Search for advanced inhibitors of YUCCA, a key enzyme in auxin biosynthesis

    Grant-in-Aid for Scientific Research(C)

    Project Year: 2014.04  -  2017.03 

    Investigator(s): ISHII Takahiro, SHIMADA Yukihisa, SOENO Kazuo 

    Direct: 4,000,000 (YEN)  Overheads: 5,200,000 (YEN)  Total: 1,200,000 (YEN)

     View Summary

    From the results of screening of own chemical library (including about 200 samples) using both YUCCA enzyme inhibition test (in vitro) and plant growth test with Arabidopsis seeds (in vivo), it was found that several extracts from the red algal genus Laurencia and sea hares, together with 2-APB known as a TRP channel inhibitor, exhibited strong inhibitory effects. Bioassay-guided fractionation of these active extracts resulted in the isolation of three halogenated laurane-type sesquiterpenes with different chemical structures from known YUCCA inhibitors. Among these active compounds, laurinterol and 2-APB showed stronger inhibitory activity than known inhibitors in the plant growth inhibition assay.