Evidence map›Paper›PMID 25675512›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

De novo production of the plant-derived alkaloid strictosidine in yeast.

Stephanie Brown, Marc Clastre, Vincent Courdavault, Sarah E O'Connor

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 176 papers.

0numbers the graph read from it
0cells of the map it votes in
176citing papers in PubMed
36.6field-weighted citation impact, top 1% 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

176 citing papers in PubMed, 463 citations in OpenAlex.

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  15. Functional Characterization ofInternational journal of molecular sciences · 2025
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116 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Stephanie BrownDepartment of Biological Chemistry, John Innes Centre, Norwich NR4 7UH, United Kingdom; and.
Marc ClastreÉquipe d'Accueil EA2106, "Biomolécules et Biotechnologies Végétales," Université François-Rabelais de Tours, 37200 Tours, France.
Vincent CourdavaultÉquipe d'Accueil EA2106, "Biomolécules et Biotechnologies Végétales," Université François-Rabelais de Tours, 37200 Tours, France.
Sarah E O'ConnorDepartment of Biological Chemistry, John Innes Centre, Norwich NR4 7UH, United Kingdom; and Sarah.O'Connor@jic.ac.uk.
John Innes Centre · GBUniversité de Tours · FR

Funding

Biotechnology and Biological Sciences Research Council BB/J009091/1European Research Council 311363
6 · The paper itself

Abstract

The monoterpene indole alkaloids are a large group of plant-derived specialized metabolites, many of which have valuable pharmaceutical or biological activity. There are ∼3,000 monoterpene indole alkaloids produced by thousands of plant species in numerous families. The diverse chemical structures found in this metabolite class originate from strictosidine, which is the last common biosynthetic intermediate for all monoterpene indole alkaloid enzymatic pathways. Reconstitution of biosynthetic pathways in a heterologous host is a promising strategy for rapid and inexpensive production of complex molecules that are found in plants. Here, we demonstrate how strictosidine can be produced de novo in a Saccharomyces cerevisiae host from 14 known monoterpene indole alkaloid pathway genes, along with an additional seven genes and three gene deletions that enhance secondary metabolism. This system provides an important resource for developing the production of more complex plant-derived alkaloids, engineering of nonnatural derivatives, identification of bottlenecks in monoterpene indole alkaloid biosynthesis, and discovery of new pathway genes in a convenient yeast host.

Indexed as

Alcohol DehydrogenaseBiosynthetic PathwaysChromatography, LiquidGenetic EngineeringMass SpectrometryPlantsSaccharomyces cerevisiaeVinca AlkaloidsAlcohol DehydrogenasestrictosidineVinca AlkaloidsCatharanthus roseusmonoterpene indole alkaloidSaccharomyces cerevisiaesecologaninstrictosidine

Identifiers

PMID25675512
PMCPMC4371906
OpenAlexW2011945340

What OpenQuestion holds

Textmetadata
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.