Evolva scientists co-author paper on diterpene biosynthesis of economically relevant commercial targets
Stereoselective biosynthesis of over 50 diterpene skeletons was demonstrated, including natural variants and novel enantiomeric or diastereomeric counterparts. Among others, the researchers produced a number of precursors for high-value diterpenoids such as forskolin (a cyclic AMP booster) and ambrox (an important fragrance molecule) by fermentation of bio-engineered strains of Saccharomyces cerevisiae (baker’s yeast).
“In this study we have once again demonstrated the synergies possible when you combine the knowledge on plant secondary metabolite biosynthesis and Evolva’s knowledge and toolset in yeast metabolic engineering,” said Evolva Senior Scientist Dr. Niels Bjerg Jensen.
“This work opens the door to the efficient and targeted production of a wealth of commercially interesting diterpenoids for both the food and flavour industries,” said Birger Lindberg Møller, Professor at the Plant Biochemistry Laboratory at the University of Copenhagen.
Original publication
J. Andersen-Ranberg, K. T. Kongstad, M. T. Nielsen, N. B. Jensen, I. Pateraki, S. S. Bach, B. Hamberger, P. Zerbe, D. Staerk, J. Bohlmann, B. L. Møller, B. Hamberger; "Expanding the Landscape of Diterpene Structural Diversity through Stereochemically Controlled Combinatorial Biosynthesis"; Angew. Chem. Int. Ed.; 2016
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Original publication
J. Andersen-Ranberg, K. T. Kongstad, M. T. Nielsen, N. B. Jensen, I. Pateraki, S. S. Bach, B. Hamberger, P. Zerbe, D. Staerk, J. Bohlmann, B. L. Møller, B. Hamberger; "Expanding the Landscape of Diterpene Structural Diversity through Stereochemically Controlled Combinatorial Biosynthesis"; Angew. Chem. Int. Ed.; 2016
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