CYP712K4 Catalyzes the C-29 Oxidation of Friedelin in the Maytenus ilicifolia Quinone Methide Triterpenoid Biosynthesis Pathway

Espinheira santa 20mar20

Fri, 20 Mar 2020

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Authors:

Bicalho, Keylla U. 1, 2, 3, 4 ; Santoni, Mariana M. 3, 4 ; Arendt, Philipp 1, 2 ; Zanelli, Cleslei F. 4 ; Furlan, Maysa 3 ; Goossens, Alain 1, 2 ; Pollier, Jacob 1, 2, 5


Abstract:

The native Brazilian plant Maytenus ilicifolia accumulates a set of quinone methide triterpenoids with important pharmacological properties, of which maytenin, pristimerin and celastrol accumulate exclusively in the root bark of this medicinal plant. The first committed step in the quinone methide triterpenoid biosynthesis is the cyclization of 2,3-oxidosqualene to friedelin, catalyzed by the oxidosqualene cyclase friedelin synthase (FRS). In this study, we produced heterologous friedelin by the expression of M. ilicifolia FRS in Nicotiana benthamiana leaves and in a Saccharomyces cerevisiae strain engineered using CRISPR/Cas9. Furthermore, friedelin-producing N. benthamiana leaves and S. cerevisiae cells were used for the characterization of CYP712K4, a cytochrome P450 from M. ilicifolia that catalyzes the oxidation of friedelin at the C-29 position, leading to maytenoic acid, an intermediate of the quinone methide triterpenoid biosynthesis pathway. Maytenoic acid produced in N. benthamiana leaves was purified and its structure was confirmed using high-resolution mass spectrometry and nuclear magnetic resonance analysis. The three-step oxidation of friedelin to maytenoic acid by CYP712K4 can be considered as the second step of the quinone methide triterpenoid biosynthesis pathway, and may form the basis for further discovery of the pathway and heterologous production of friedelanes and ultimately quinone methide triterpenoids.


1   Department of Plant Biotechnology and Bioinformatics, Ghent University, 9052 Ghent, Belgium

2   VIB Center for Plant Systems Biology, 9052 Ghent, Belgium

3   Department of Organic Chemistry, Institute of Chemistry, Sao Paulo State University (UNESP), Araraquara, Sao Paulo, Brazil

4   Department of Biological Sciences, School of Pharmaceutical Sciences, Sao Paulo State University (UNESP), Araraquara, Sao Paulo, Brazil

5   VIB Metabolomics Core, 9052 Ghent, Belgium


Link to article:   https://academic.oup.com/pcp/article/60/11/2510/5539493

 

 

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