Evidence map›Paper›PMID 37391700›Full record

ArticleBMC plant biology2023

The revealing of a novel double bond reductase related to perilla ketone biosynthesis in Perilla frutescens.

Peina Zhou, Yongfang Shao, Zheng Jiang, Jingjie Dang, Cheng Qu, Qinan Wu

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

9 citing papers in PubMed, 12 citations in OpenAlex.

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  7. Comprehensive Review ofFoods (Basel, Switzerland) · 2025
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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

6 authors at 1 institution in 1 country.

Peina Zhou *College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Yongfang Shao *College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Zheng JiangCollege of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Jingjie DangCollege of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Cheng QuCollege of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China. qucheng@njucm.edu.cn.
Qinan WuCollege of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China. wuqn@njucm.edu.cn.
Nanjing University of Chinese Medicine · CN

Funding

National Natural Science Foundation of China 81973435National Natural Science Foundation of China 82204597
6 · The paper itself

Abstract

backgroundPerilla frutescens is widely used as both a medicine and a food worldwide. Its volatile oils are its active ingredients, and, based on the different volatile constituents, P. frutescens can be divided into several chemotypes, with perilla ketone (PK) being the most common. However, the key genes involved in PK biosynthesis have not yet been identified.

resultsIn this study, metabolite constituents and transcriptomic data were compared in leaves of different levels. The variation in PK levels was the opposite of that of isoegoma ketone and egoma ketone in leaves at different levels. Based on transcriptome data, eight candidate genes were identified and successfully expressed in a prokaryotic system. Sequence analysis revealed them to be double bond reductases (PfDBRs), which are members of the NADPH-dependent, medium-chain dehydrogenase/reductase (MDR) superfamily. They catalyze the conversion of isoegoma ketone and egoma ketone into PK in in vitro enzymatic assays. PfDBRs also showed activity on pulegone, 3-nonen-2-one, and 4-hydroxybenzalacetone. In addition, several genes and transcription factors were predicted to be associated with monoterpenoid biosynthesis, and their expression profiles were positively correlated with variations in PK abundance, suggesting their potential functions in PK biosynthesis.

conclusionsThe eight candidate genes encoding a novel double bond reductase related to perilla ketone biosynthesis were identified in P. frutescens, which carries similar sequences and molecular features as the MpPR and NtPR from Nepeta tenuifolia and Mentha piperita, respectively. These findings not only reveal the pivotal roles of PfDBR in exploring and interpreting PK biological pathway but also contribute to facilitating future studies on this DBR protein family.

Indexed as

PerillaPerilla frutescensKetonesMonoterpenesOxidoreductasesKetonesMonoterpenesOxidoreductasesperilla ketoneDouble bond reductaseEnzyme assaysPerilla frutescensPerilla ketone biosynthesisTranscriptome

Identifiers

PMID37391700
PMCPMC10311769
OpenAlexW4382776551

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.