Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Diterpene biosynthesis"'
Autor:
Mafu, Sibongile, Karunanithi, Prema Sambandaswami, Palazzo, Teresa Ann, Harrod, Bronwyn Lee, Rodriguez, Selina Marakana, Mollhoff, Iris Natalie, O’Brien, Terrence Edward, Tong, Shen, Fiehn, Oliver, Tantillo, Dean J., Bohlmann, Jörg, Zerbe, Philipp
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2017 Jan . 114(5), 974-979.
Externí odkaz:
https://www.jstor.org/stable/26479121
Autor:
Changbiao Chi, Donghui Yang, Hongli Jia, Annan Li, Luqi Huang, Jiahui Yu, Qingxia Xu, Zhengdong Wang, Ming Ma, Fuling Yin, Baiying Xing, Xueyang Ma, Tan Liu, Yuanjie Ge, Juan Guo
Publikováno v:
Communications Chemistry, Vol 4, Iss 1, Pp 1-11 (2021)
Pimarane-type diterpenoids are widely distributed in all domains of life, but no structures or catalytic mechanisms of pimarane-type diterpene synthases (DTSs) have been characterized. Here, we report that two class I DTSs, Sat1646 and Stt4548, each
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bbf747b33519a48a9a45bd40ea9cb3e
https://doi.org/10.1038/s42004-021-00578-z
https://doi.org/10.1038/s42004-021-00578-z
Autor:
Jeroen S. Dickschat
This article gives an overview of the recent developments in diterpene biosynthesis. The section is structured by the producing organisms, starting with diterpenes from bacteria, followed by fungi and plants, and finishing with social amoebae that we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8f0f581ae2b1fa29d696552ae9e5abb
https://doi.org/10.1016/b978-0-12-409547-2.14624-4
https://doi.org/10.1016/b978-0-12-409547-2.14624-4
Autor:
Yoshimi Yamamura
Publikováno v:
ASPB PLANT BIOLOGY 2020.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0576b7059a735f9197172917f41113df
https://doi.org/10.46678/pb.20.107440
https://doi.org/10.46678/pb.20.107440
Autor:
Jeroen S. Dickschat
Publikováno v:
Angewandte Chemie (International ed. in English). 58(45)
This Minireview summarises recent developments in the biosynthesis of diterpenes by diterpene synthases in bacteria. It is structured by the class of enzyme involved in the first committed step towards diterpenes, starting with type I diterpene synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0676f0e21e7e6d5b27edae45cf7136a
https://pubmed.ncbi.nlm.nih.gov/31183935
https://pubmed.ncbi.nlm.nih.gov/31183935
Publikováno v:
The FASEB Journal. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d66a149d957b3d19a4567c589f264c81
https://doi.org/10.1096/fasebj.2019.33.1_supplement.lb311
https://doi.org/10.1096/fasebj.2019.33.1_supplement.lb311
Publikováno v:
Angewandte Chemie (International ed. in English). 58(27)
Three diterpene synthases from actinomycetes have been studied. The first enzyme from Streptomyces cattleya produced the novel compound cattleyene. The other two enzymes from Nocardia testacea and Nocardia rhamnosiphila were identified as phomopsene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d52705af7911d1c46d6c525b12e48f1d
https://pubmed.ncbi.nlm.nih.gov/31034729
https://pubmed.ncbi.nlm.nih.gov/31034729
Publikováno v:
Planta Medica. 81:S1-S381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f25939f17f06fae5ad988bf26590f89c
https://doi.org/10.1055/s-0036-1596189
https://doi.org/10.1055/s-0036-1596189
Akademický článek
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Autor:
Stephen P. Marsden, Matthew Lilburn, Axel Pahl, Philip G. E. Craven, James D. Firth, Adam Nelson
Publikováno v:
Chemical communications (Cambridge, England). 52(63)
A synthetic approach to diverse scaffolds was developed that was inspired by diterpene biosynthesis. Initial scaffolds, generated using Diels–Alder reactions of furyl-functionalised amines, were transformed into alternative scaffolds using cleavage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54082932ba9337a27b5c5c4039be3cc9
https://pubmed.ncbi.nlm.nih.gov/27424656
https://pubmed.ncbi.nlm.nih.gov/27424656