Evidence map›Paper›PMID 26343621›Full record

ArticleMolecules (Basel, Switzerland)2015

Molecular Cloning and Characterization of a Xanthone Prenyltransferase from Hypericum calycinum Cell Cultures.

Tobias Fiesel, Mariam Gaid, Andreas Müller, Joana Bartels, Islam El-Awaad, Till Beuerle, Ludger Ernst, Sönke Behrends, Ludger Beerhues

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Reverse prenylation in plants by non-canonical aromatic prenyltransferases.The Plant journal : for cell and molecular biology · 2025
    Article
  4. Review
  5. Xanthone Biosynthetic Pathway in Plants: A Review.Frontiers in plant science · 2022
    Review
  6. Review
  7. Isolation ofCommunications biology · 2019
    Article
  8. Molecular architectures of benzoic acid-specific type III polyketide synthases.Acta crystallographica. Section D, Structural biology · 2017
    Article
  9. Review
  10. 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

9 authors.

Tobias FieselInstitute of Pharmaceutical Biology, Technische Universität Braunschweig, Mendelssohnstraße 1, Braunschweig 38106, Germany. t.fiesel@tu-bs.de.
Mariam GaidInstitute of Pharmaceutical Biology, Technische Universität Braunschweig, Mendelssohnstraße 1, Braunschweig 38106, Germany. m.gaid@tu-bs.de.
Andreas MüllerInstitute of Pharmaceutical Biology, Technische Universität Braunschweig, Mendelssohnstraße 1, Braunschweig 38106, Germany. der.andreas.mueller@gmx.net.
Joana BartelsCenter of Pharmaceutical Engineering (PVZ), Technische Universität Braunschweig, Franz-Liszt-Straße 35 A, Braunschweig 38106, Germany. jo.bartels@tu-bs.de.
Islam El-AwaadInstitute of Pharmaceutical Biology, Technische Universität Braunschweig, Mendelssohnstraße 1, Braunschweig 38106, Germany. i.el-awaad@tu-bs.de.
Till BeuerleInstitute of Pharmaceutical Biology, Technische Universität Braunschweig, Mendelssohnstraße 1, Braunschweig 38106, Germany. t.beuerle@tu-bs.de.
Ludger ErnstCentral NMR Laboratory, Technische Universität Braunschweig, Hagenring 30, Braunschweig 38106, Germany. l.ernst@tu-bs.de.
Sönke BehrendsCenter of Pharmaceutical Engineering (PVZ), Technische Universität Braunschweig, Franz-Liszt-Straße 35 A, Braunschweig 38106, Germany. s.behrends@tu-bs.de.
Ludger BeerhuesInstitute of Pharmaceutical Biology, Technische Universität Braunschweig, Mendelssohnstraße 1, Braunschweig 38106, Germany. l.beerhues@tu-bs.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In plants, prenylation of metabolites is widely distributed to generate compounds with efficient defense potential and distinct pharmacological activities profitable to human health. Prenylated compounds are formed by members of the prenyltransferase (PT) superfamily, which catalyze the addition of prenyl moieties to a variety of acceptor molecules. Cell cultures of Hypericum calycinum respond to elicitor treatment with the accumulation of the prenylated xanthone hyperxanthone E. A cDNA encoding a membrane-bound PT (HcPT) was isolated from a subtracted cDNA library and transcript preparations of H. calycinum. An increase in the HcPT transcript level preceded hyperxanthone E accumulation in cell cultures of H. calycinum treated with elicitor. The HcPT cDNA was functionally characterized by expression in baculovirus-infected insect cells. The recombinant enzyme catalyzed biosynthesis of 1,3,6,7-tetrahydroxy-8-prenylxanthone through regiospecific C-8 prenylation of 1,3,6,7-tetrahydroxyxanthone, indicating its involvement in hyperxanthone E formation. The enzymatic product shared significant structural features with the previously reported cholinesterase inhibitor γ-mangostin. Thus, our findings may offer a chance for semisynthesis of new active agents to be involved in the treatment of Alzheimer's disease.

Indexed as

Cloning, MolecularDimethylallyltranstransferaseGene LibraryHypericumModels, MolecularPlant ProteinsProtein ConformationRecombinant ProteinsXanthonesDimethylallyltranstransferasePlant ProteinsRecombinant ProteinsXanthonesAlzheimer’s diseasearomatic prenyltransferaseHypericummembrane-bound enzymexanthone

Identifiers

PMID26343621
PMCPMC6332024

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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.