Evidence map›Paper›PMID 30531909›Full record

ArticleNature chemical biology2019

Uncoupled activation and cyclization in catmint reductive terpenoid biosynthesis.

Benjamin R Lichman, Mohamed O Kamileen, Gabriel R Titchiner, Gerhard Saalbach, Clare E M Stevenson, David M Lawson, Sarah E O'Connor

Abstract read
In one paragraph

Article in Nature chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Haplotype-resolved genome ofHorticulture research · 2025
    Article
  5. Via Air or Rhizosphere: The Phytotoxicity ofPlants (Basel, Switzerland) · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Plant terpene specialized metabolism: complex networks or simple linear pathways?The Plant journal : for cell and molecular biology · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Biosynthesis of iridoid sex pheromones in aphids.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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 1 institution in 1 country.

Benjamin R LichmanThe John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.ORCID http://orcid.org/0000-0002-0033-1120
Mohamed O KamileenThe John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.
Gabriel R TitchinerThe John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.ORCID http://orcid.org/0000-0002-6378-9884
Gerhard SaalbachThe John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.
Clare E M StevensonThe John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.ORCID http://orcid.org/0000-0001-6695-8201
David M LawsonThe John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.ORCID http://orcid.org/0000-0002-7637-4303
Sarah E O'ConnorThe John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK. sarah.Oconnor@jic.ac.uk.ORCID http://orcid.org/0000-0003-0356-6213
John Innes Centre · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L014130/1Biotechnology and Biological Sciences Research Council BBS/E/J/000PR9790European Research Council 311363
6 · The paper itself

Abstract

Terpene synthases typically form complex molecular scaffolds by concerted activation and cyclization of linear starting materials in a single enzyme active site. Here we show that iridoid synthase, an atypical reductive terpene synthase, catalyzes the activation of its substrate 8-oxogeranial into a reactive enol intermediate, but does not catalyze the subsequent cyclization into nepetalactol. This discovery led us to identify a class of nepetalactol-related short-chain dehydrogenase enzymes (NEPS) from catmint (Nepeta mussinii) that capture this reactive intermediate and catalyze the stereoselective cyclisation into distinct nepetalactol stereoisomers. Subsequent oxidation of nepetalactols by NEPS1 provides nepetalactones, metabolites that are well known for both insect-repellent activity and euphoric effects in cats. Structural characterization of the NEPS3 cyclase reveals that it binds to NAD

Indexed as

Alkyl and Aryl TransferasesBinding SitesBridged Bicyclo Compounds, HeterocyclicCrystallography, X-RayCyclizationIridoidsMonoterpenesNepetaOxidation-ReductionOxidoreductasesPlant ProteinsSerineAlkyl and Aryl TransferasesBridged Bicyclo Compounds, HeterocyclicIridoidsMonoterpenesnepetalactolOxidoreductasesPlant ProteinsSerineterpene synthase

Identifiers

PMID30531909
PMCPMC6513753
OpenAlexW2885313085

What OpenQuestion holds

Textmetadata
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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.