Evangelos Tatsis

Affiliations: 
CAS Center for Excellence in Molecular Plant Sciences 
Area:
natural products biosynthesis
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"Evangelos Tatsis"
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Publications

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Li H, Wu S, Lin R, et al. (2023) The genomes of medicinal skullcaps reveal the polyphyletic origins of clerodane diterpene biosynthesis in the family Lamiaceae. Molecular Plant
Wang Z, Xiao Y, Wu S, et al. (2022) Deciphering and reprogramming the cyclization regioselectivity in bifurcation of indole alkaloid biosynthesis. Chemical Science. 13: 12389-12395
Langley C, Tatsis E, Hong B, et al. (2022) Expansion of the Catalytic Repertoire of Alcohol Dehydrogenases in Plant Metabolism. Angewandte Chemie (International Ed. in English)
Howes MR, Quave CL, Collemare J, et al. (2020) Molecules from nature: Reconciling biodiversity conservation and global healthcare imperatives for sustainable use of medicinal plants and fungi Plants, People, Planet. 2: 463-481
Franke J, Kim J, Hamilton JP, et al. (2018) Gene discovery in Gelsemium highlights conserved gene clusters in monoterpene indole alkaloid biosynthesis. Chembiochem : a European Journal of Chemical Biology
Casini A, Chang FY, Eluere R, et al. (2018) A pressure test to make 10 molecules in 90 days: External evaluation of methods to engineer biology. Journal of the American Chemical Society
Stavrinides A, Tatsis E, Dang TT, et al. (2018) Discovery of a short chain dehydrogenase from Catharanthus roseus that produces a novel monoterpene indole alkaloid. Chembiochem : a European Journal of Chemical Biology
Tatsis EC, Carqueijeiro I, Dugé de Bernonville T, et al. (2017) A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate. Nature Communications. 8: 316
Dang TT, Franke J, Tatsis EC, et al. (2017) Dual catalytic activity of a cytochrome P450 controls bifurcation at a metabolic branch point of alkaloid biosynthesis in Rauwolfia serpentina. Angewandte Chemie (International Ed. in English)
Payne RM, Xu D, Foureau E, et al. (2017) An NPF transporter exports a central monoterpene indole alkaloid intermediate from the vacuole. Nature Plants. 3: 16208
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