4.7 Article

Piper nigrum CYP719A37 Catalyzes the Decisive Methylenedioxy Bridge Formation in Piperine Biosynthesis

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PLANTS-BASEL
卷 10, 期 1, 页码 -

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MDPI
DOI: 10.3390/plants10010128

关键词

black pepper; cytochrome P450; enzyme activity; methylenedioxy bridge; piperine; Piper nigrum; yeast expression

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  1. Deutsche Forschungsgemeinschaft (DFG) [VO 719/15-1/2]

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The biosynthesis of piperine in black pepper is still largely unknown, but a study using RNA-sequencing and yeast functional expression found that a specific cytochrome P450 transcript expressed in immature black pepper fruits is responsible for the formation of the methylenedioxy bridge characteristic of piperine. The enzyme identified, classified as CYP719A37, has specificity towards feruperic acid as a substrate and plays a crucial role in the biosynthesis process of piperine.
Black pepper (Piper nigrum) is among the world's most popular spices. Its pungent principle, piperine, has already been identified 200 years ago, yet the biosynthesis of piperine in black pepper remains largely enigmatic. In this report we analyzed the characteristic methylenedioxy bridge formation of the aromatic part of piperine by a combination of RNA-sequencing, functional expression in yeast, and LC-MS based analysis of substrate and product profiles. We identified a single cytochrome P450 transcript, specifically expressed in black pepper immature fruits. The corresponding gene was functionally expressed in yeast (Saccharomyces cerevisiae) and characterized for substrate specificity with a series of putative aromatic precursors with an aromatic vanilloid structure. Methylenedioxy bridge formation was only detected when feruperic acid (5-(4-hydroxy-3-methoxyphenyl)-2,4-pentadienoic acid) was used as a substrate, and the corresponding product was identified as piperic acid. Two alternative precursors, ferulic acid and feruperine, were not accepted. Our data provide experimental evidence that formation of the piperine methylenedioxy bridge takes place in young black pepper fruits after a currently hypothetical chain elongation of ferulic acid and before the formation of the amide bond. The partially characterized enzyme was classified as CYP719A37 and is discussed in terms of specificity, storage, and phylogenetic origin of CYP719 catalyzed reactions in magnoliids and eudicots.

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