CYP98A22, a phenolic ester 3’-hydroxylase specialized in the synthesis of chlorogenic acid, as a new tool for enhancing the furanocoumarin concentration in Ruta graveolens

CYP98A22 — 3′-гидроксилаза фенольных эфиров, специализированная в биосинтезе хлорогеновой кислоты, как новый инструмент для повышения концентрации фуранокумаринов у Ruta graveolens
Pascaline Ullmann, Danièle Werck‐Reichhart, Frédéric Bourgaud, Alain Hehn, Alexandre Olry, Sébastien Doerper, Fazeelat Karamat, Guilhem Vialart
2012-08-29

CYP98A22Ruta graveolenschlorogenic acidcytochrome P450 hydroxylasefuranocoumarin biosynthesis
BACKGROUND: Furanocoumarins are molecules with proven therapeutic properties and are produced in only a small number of medicinal plant species such as Ruta graveolens. In vivo, these molecules play a protective role against phytophageous insect attack. Furanocoumarins are members of the phenylpropanoids family, and their biosynthetic pathway is initiated from p-coumaroyl coA. The enzymes belonging to the CYP98A cytochrome P450 family have been widely described as being aromatic meta-hydroxylases of various substrates, such as p-coumaroyl ester derivatives, and are involved in the synthesis of coumarins such as scopoletin. In furanocoumarin-producing plants, these enzymes catalyze the step directly downstream of the junction with the furanocoumarin biosynthetic pathway and might indirectly impact their synthesis. RESULTS: In this work, we describe the cloning and functional characterization of the first CYP98A encoding gene isolated from R. graveolens. Using Nicotiana benthamiana as a heterologous expression system, we have demonstrated that this enzyme adds a 3-OH to p-coumaroyl ester derivatives but is more efficient to convert p-coumaroyl quinate into chlorogenic acid than to metabolize p-coumaroyl shikimate. Plants exposed to UV-B stress showed an enhanced expression level of the corresponding gene. The R. graveolens cyp98a22 open reading frame and the orthologous Arabidopsis thaliana cyp98a3 open reading frame were overexpressed in stable transgenic Ruta plants. Both plant series were analyzed for their production of scopoletin and furanocoumarin. A detailed analysis indicates that both genes enhance the production of furanocoumarins but that CYP98A22, unlike CYP98A3, doesn't affect the synthesis of scopoletin. CONCLUSIONS: The overexpression of CYP98A22 positively impacts the concentration of furanocoumarins in R. graveolens. This gene is therefore a valuable tool to engineer plants with improved therapeutical values that might also be more resistant to phytophageous insects.
1
CYP98A22 is the first CYP98A gene characterized from Ruta graveolens and catalyzes 3′-hydroxylation of p-coumaroyl ester derivatives.
2
CYP98A22 preferentially converts p-coumaroyl quinate into chlorogenic acid rather than metabolizing p-coumaroyl shikimate.
3
Stable overexpression of CYP98A22 or Arabidopsis CYP98A3 enhances furanocoumarin production in transgenic R. graveolens plants.
4
UV-B stress increases expression of the R. graveolens CYP98A22 gene.
5
Unlike CYP98A3, CYP98A22 increases furanocoumarin concentration without affecting scopoletin biosynthesis, making it a potential engineering tool for improving therapeutic value and phytophage resistance.

CYP98A22-mediated phenylpropanoid metabolism and furanocoumarin production in transgenic Ruta graveolens plants

The effects of CYP98A22 overexpression on chlorogenic acid, scopoletin, and furanocoumarin production, including substrate specificity and response to UV-B stress

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2012-08-29
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Pascaline Ullmann
Danièle Werck‐Reichhart
Frédéric Bourgaud
Alain Hehn
Alexandre Olry
Sébastien Doerper
Fazeelat Karamat
Guilhem Vialart
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