Evidence map›Paper›PMID 25884984›Full record

ArticleBMC plant biology2015

Evidence of capsaicin synthase activity of the Pun1-encoded protein and its role as a determinant of capsaicinoid accumulation in pepper.

Kana Ogawa, Katsunori Murota, Hanako Shimura, Misaki Furuya, Yasuko Togawa, Takeshi Matsumura, Chikara Masuta

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 55 citations in OpenAlex.

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  15. Discovery of novel unfunctionalBreeding science · 2019
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  16. Article
  17. Mutation in the putative ketoacyl-ACP reductase CaKR1 induces loss of pungency in Capsicum.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2019
    Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Kana OgawaGraduate School of Agriculture, Hokkaido University, Sapporo, 060-8589, Japan. kana9999102@yahoo.co.jp.
Katsunori MurotaGraduate School of Agriculture, Hokkaido University, Sapporo, 060-8589, Japan. murota@abs.agr.hokudai.ac.jp.
Hanako ShimuraGraduate School of Agriculture, Hokkaido University, Sapporo, 060-8589, Japan. hana@res.agr.hokudai.ac.jp.
Misaki FuruyaGraduate School of Agriculture, Hokkaido University, Sapporo, 060-8589, Japan. fam.ggb.836@gmail.com.
Yasuko TogawaGraduate School of Agriculture, Hokkaido University, Sapporo, 060-8589, Japan. ytogawa@res.agr.hokudai.ac.jp.
Takeshi MatsumuraPlant Molecular Technology Research Group, Research Institute of Bioproduction, National Institute of Advanced Industrial Science and Technology, Sapporo, 062-8517, Japan. matsumura-t@aist.go.jp.
Chikara MasutaGraduate School of Agriculture, Hokkaido University, Sapporo, 060-8589, Japan. masuta@res.agr.hokudai.ac.jp.
Hokkaido University · JPNational Institute of Advanced Industrial Science and Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Gene Expression Regulation, PlantCapsaicinCapsicumPlant ProteinsProtoplastsCapsaicinPlant Proteins

Identifiers

PMID25884984
PMCPMC4386094
OpenAlexW2044677127

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.