Zobrazeno 1 - 10
of 276
pro vyhledávání: '"Hiromasa, Kiyota"'
Autor:
Christopher J. Vavricka, Shunsuke Takahashi, Naoki Watanabe, Musashi Takenaka, Mami Matsuda, Takanobu Yoshida, Ryo Suzuki, Hiromasa Kiyota, Jianyong Li, Hiromichi Minami, Jun Ishii, Kenji Tsuge, Michihiro Araki, Akihiko Kondo, Tomohisa Hasunuma
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022)
Producing plant secondary metabolites by microbes is limited by the known enzymatic reactions. Here, the authors apply machine learning to predict missing link enzymes of benzylisoquinoline alkaloid (BIA) biosynthesis in Papaver somniferum, and valid
Externí odkaz:
https://doaj.org/article/baf664b334934b1d89704e14d973d831
Autor:
Christopher J. Vavricka, Takanobu Yoshida, Yuki Kuriya, Shunsuke Takahashi, Teppei Ogawa, Fumie Ono, Kazuko Agari, Hiromasa Kiyota, Jianyong Li, Jun Ishii, Kenji Tsuge, Hiromichi Minami, Michihiro Araki, Tomohisa Hasunuma, Akihiko Kondo
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-11 (2019)
Bioproduction of tetrahydropapaveroline (THP) is limited by the specificity of monoamine oxidase (MAO). Here, the authors identify an insect 3,4-dihydroxyphenylacetaldehyde synthase (DHPAAS) that can bypass MAO for direct aldehyde production and demo
Externí odkaz:
https://doaj.org/article/cff5bceaa4c341b49a36d8f2870f8cb6
Autor:
Christopher J. Vavricka, Chiaki Muto, Tomohisa Hasunuma, Yoshinobu Kimura, Michihiro Araki, Yan Wu, George F. Gao, Hiroshi Ohrui, Minoru Izumi, Hiromasa Kiyota
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract The design, synthesis and application of N-acetylneuraminic acid-derived compounds bearing anomeric sulfo functional groups are described. These novel compounds, which we refer to as sulfo-sialic acid analogues, include 2-decarboxy-2-deoxy-2
Externí odkaz:
https://doaj.org/article/d71999dbcf09495f926bec89b3dbfc54
Autor:
Koji Ito, Ryota Kataoka, Shunki Katayama, Hiromasa Kiyota, Ahmad Mahmood, Takashi Kikuchi, Takashi Sato, Futa Sakakibara, Kazuhiro Takagi
Publikováno v:
Journal of Agricultural and Food Chemistry. 70:770-776
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8dfa3c91633ffbdb29b83b8806c99d2
https://doi.org/10.1021/acs.jafc.1c05987
https://doi.org/10.1021/acs.jafc.1c05987
Autor:
Shunki Katayama, Mitsuki Nishimoto, Tatsuya Ura, Taiki Ishimoto, Kousuke Ida, Yuki Sato, Christopher J. Vavricka, Minoru Izumi, Hiromasa Kiyota
Maoecrystal V is a highly oxidized and rearranged norterpenoid isolated from the Chinese herb, Isodon eriocalyx. A synthetic route for the C/D/E-ring core compound of maoecrystal V has been developed. Introduction of the C1 fragment to the D/E-ring c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6b77a7bfc477638983e2a2836ddb90
Publikováno v:
Nematological Research (Japanese Journal of Nematology). 51:33-36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fceb41afeb8ef7fe8aeb9cf85a10febb
https://doi.org/10.3725/jjn.51.33
https://doi.org/10.3725/jjn.51.33
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2556
Depending on the strain, influenza A virus causes animal, zoonotic, pandemic, or seasonal influenza with varying degrees of severity. Two surface glycoprotein spikes, hemagglutinin (HA) and neuraminidase (NA), are the most important influenza A virus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c5b016874f16b83d7cc046bd3fc1a86
https://pubmed.ncbi.nlm.nih.gov/36175642
https://pubmed.ncbi.nlm.nih.gov/36175642
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2556
Methods to synthesize influenza virus inhibitors with fluoro, phosphono, and/or sulfo functional groups are described. The resulting sialic acid analogues are produced from the natural substrate N-acetylneuraminic acid as starting material. Fluoresce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26d19cf72c0641c98edc72a5577a74bd
https://pubmed.ncbi.nlm.nih.gov/36175641
https://pubmed.ncbi.nlm.nih.gov/36175641
Autor:
Hiromasa KIYOTA1 kiyota@okayama-u.ac.jp
Publikováno v:
Journal of Pesticide Science. 2020, Vol. 45 Issue 3, p177-183. 7p.
Autor:
Christopher J. Vavricka, Takanobu Yoshida, Yuki Kuriya, Shunsuke Takahashi, Teppei Ogawa, Fumie Ono, Kazuko Agari, Hiromasa Kiyota, Jianyong Li, Jun Ishii, Kenji Tsuge, Hiromichi Minami, Michihiro Araki, Tomohisa Hasunuma, Akihiko Kondo
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
In the original version of this Article, the abbreviation of 3,4-dihydroxyphenylacetaldehyde synthase presented in the first paragraph of the Discussion section was given incorrectly as DYPAA. The correct abbreviation for this enzyme is DHPAAS. This
Externí odkaz:
https://doaj.org/article/560dc530b2c64e6cb9230b7cd891a82f