Abstract

BackgroundCapsaicinoids, including capsaicin and its analogs, are responsible for the pungency of pepper (Capsicum species) fruits. Even though capsaicin is familiar and used daily by humans, the genes involved in the capsaicin biosynthesis pathway have not been well characterized. The putative aminotransferase (pAMT) and Pungent gene 1 (Pun1) proteins are believed to catalyze the second to last and the last steps in the pathway, respectively, making the Pun1 protein the putative capsaicin synthase. However, there is no direct evidence that Pun1 has capsaicin synthase activity.ResultsTo verify that the Pun1 protein actually plays a role in capsaicin production, we generated anti-Pun1 antibodies against an Escherichia coli-synthesized Pun1 protein and used them to antagonize endogenous Pun1 activity. To confirm the anti-Pun1 antibodies’ specificity, we targeted Pun1 mRNA using virus-induced gene silencing. In the Pun1-down-regulated placental tissues, the accumulated levels of the Pun1 protein, which was identified on a western blot using the anti-Pun1 antibodies, were reduced, and simultaneously, capsaicin accumulations were reduced in the same tissues. In the de novo capsaicin synthesis in vitro cell-free assay, which uses protoplasts isolated from placental tissues, capsaicin synthesis was inhibited by the addition of anti-Pun1 antibodies. We next analyzed the expression profiles of pAMT and Pun1 in various pepper cultivars and found that high levels of capsaicin accumulation always accompanied high expression levels of both pAMT and Pun1, indicating that both genes are important for capsaicin synthesis. However, comparisons of the accumulated levels of vanillylamine (a precursor of capsaicin) and capsaicin between pungent and nonpungent cultivars revealed that vanillylamine levels in the pungent cultivars were very low, probably owing to its rapid conversion to capsaicin by Pun1 soon after synthesis, and that in nonpungent cultivars, vanillylamine accumulated to quite high levels owing to the lack of Pun1.ConclusionsUsing a newly developed protoplast-based assay for de novo capsaicin synthesis and the anti-Pun1 antibodies, we successfully demonstrated that the Pun1 gene and its gene product are involved in capsaicin synthesis. The analysis of the vanillylamine accumulation relative to that of capsaicin indicated that Pun1 was the primary determinant of their accumulation levels.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-015-0476-7) contains supplementary material, which is available to authorized users.

Highlights

  • Capsaicinoids, including capsaicin and its analogs, are responsible for the pungency of pepper (Capsicum species) fruits

  • We tested whether the antibodies crossreact with another acyltransferase, hydroxycinnamoyl transferase (HCT), which is listed as a candidate enzyme in the capsaicinoid synthesis pathway [21,22]

  • The reduced level of the Pungent gene 1 (Pun1) protein detected by our antibodies reasonably reflected the reduced levels of capsaicinoid, and we concluded that the specificity of the antibodies for the Pun1 protein was satisfactory

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Summary

Introduction

Capsaicinoids, including capsaicin and its analogs, are responsible for the pungency of pepper (Capsicum species) fruits. Capsaicinoids are used in the human diet for their distinct pungent taste and bioactivities, such as thermogenesis [3,4] and the suppression of fat accumulation [5]. They are used for pharmaceutical purposes because they have potential bioactivities that are ascribed to antioxidants [6] and anti-cancer agents [7]. Nonpungent cultivars have been shown either to accumulate very few capsaicinoids or to accumulate capsinoids, such as capsiate, which are capsaicinoid analogs (branched-chain fatty acid ester of vanillyl alcohol) that lack the stimuli of the capsaicinoids [8]

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