Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nanami Shiotani"'
Autor:
Takatoshi Wakabayashi, Daisuke Moriyama, Ayumi Miyamoto, Hironori Okamura, Nanami Shiotani, Nobuhiro Shimizu, Masaharu Mizutani, Hirosato Takikawa, Yukihiro Sugimoto
Publikováno v:
Frontiers in Plant Science, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/d484d1cd3e9540aaac360434d2d2c8ac
Autor:
Takatoshi Wakabayashi, Daisuke Moriyama, Ayumi Miyamoto, Hironori Okamura, Nanami Shiotani, Nobuhiro Shimizu, Masaharu Mizutani, Hirosato Takikawa, Yukihiro Sugimoto
Publikováno v:
Frontiers in Plant Science, Vol 13 (2022)
Canonical strigolactones (SLs), such as orobanchol, consist of a tricyclic lactone ring (ABC-ring) connected to a methylbutenolide (D-ring). Tomato plants have been reported to produce not only orobanchol but also various canonical SLs related to the
Externí odkaz:
https://doaj.org/article/0e036c7486774b4caf63f2f0deee40a3
Autor:
Masato Homma, Takatoshi Wakabayashi, Yoshitaka Moriwaki, Nanami Shiotani, Takumi Shigeta, Kazuki Isobe, Atsushi Okazawa, Daisaku Ohta, Tohru Terada, Kentaro Shimizu, Masaharu Mizutani, Hirosato Takikawa, Yukihiro Sugimoto
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 6/25/2024, Vol. 121 Issue 26, p1-11, 44p
Autor:
Daisuke Moriyama, Takatoshi Wakabayashi, Nanami Shiotani, Shunya Yamamoto, Yui Furusato, Kohki Yabe, Masaharu Mizutani, Hirosato Takikawa, Yukihiro Sugimoto
Publikováno v:
Bioscience, Biotechnology, and Biochemistry.
Strigolactones (SLs) known as rhizosphere signaling molecules and plant hormones regulating shoot architecture, are classified into two distinct groups, canonical and non-canonical SLs based on their structures. Avenaol, a non-canonical SL found in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec07706b5c027ff092150ab460cd035
https://doi.org/10.1093/bbb/zbac069
https://doi.org/10.1093/bbb/zbac069
Autor:
Hikaru Shinde, Yukihiro Sugimoto, Nanami Shiotani, Takatoshi Wakabayashi, Hirosato Takikawa, Masaharu Mizutani, Shunya Yamamoto
Heliolactone is a non-canonical strigolactone isolated from sunflower root exudates. We have previously demonstrated that exogenously administered carlactonoic acid (CLA) was converted to heliolactone in sunflower. The conversion of CLA to heliolacto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::474763da8eb568d4d6e0a2abcba6c4f7
Autor:
Hironori Okamura, Takatoshi Wakabayashi, Nanami Shiotani, Hirosato Takikawa, Yusuke Ogura, Yukihiro Sugimoto
Publikováno v:
Tetrahedron Letters. 85:153469
Strigolactones, a class of apocarotenoids, are known to function as rhizosphere semiochemicals and plant hormones. Canonical strigolactones consist of a tricyclic lactone (ABC-rings) and a butenolide moiety (D-ring), and their biosynthesis has been e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12dd3212e8f87c00db814850da5fb478
https://doi.org/10.1016/j.tetlet.2021.153469
https://doi.org/10.1016/j.tetlet.2021.153469
Autor:
Izumi Shirakawa, Arata Yajima, Ken Ishigami, Nanami Shiotani, Ryo Katsuta, Hazuki Murakawa, Tatsuo Saito, Kazuya Ueda
Publikováno v:
Tetrahedron. 92:132253
The enantioselective synthesis of aromatic bisabolanes, such as 1,3,5-bisabolatrien-7-ol, peniciaculin A and B, and hydroxysydonic acid, has been described. Our methodology for the total synthesis of aromatic bisabolanes involves the stereoselective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::517646685d1585790f2afe43d59af80e
https://doi.org/10.1016/j.tet.2021.132253
https://doi.org/10.1016/j.tet.2021.132253
Publikováno v:
Tetrahedron Letters. 68:152922
Strigolactones are a group of apocarotenoids known as rhizosphere semiochemicals and phytohormones. Canonical strigolactone consists of a tricyclic lactone (ABC-rings) and a butenolide moiety (D-ring). Although strigolactone biosynthesis has been ext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ad0905e67058795ac350fd241eec1f3
https://doi.org/10.1016/j.tetlet.2021.152922
https://doi.org/10.1016/j.tetlet.2021.152922