Evidence map›Paper›PMID 35732945›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Generating an EMS Mutant Population and Rapid Mutant Screening by Thin-Layer Chromatography Enables the Studies of Monoterpenoid Indole Alkaloids Biosynthesis in Catharanthus Roseus.

Mohammadamin Shahsavarani, Maisha Farzana, Vincenzo De Luca, Yang Qu

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Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 country.

Mohammadamin ShahsavaraniDepartment of Chemical Engineering, University of New Brunswick, Fredericton, NB, Canada.
Maisha FarzanaDepartment of Chemistry, University of New Brunswick, Fredericton, NB, Canada.
Vincenzo De LucaDepartment of Biological Sciences, Brock University, St. Catharines, ON, Canada.
Yang QuDepartment of Chemical Engineering, University of New Brunswick, Fredericton, NB, Canada. yang.qu@unb.ca.
University of New Brunswick · CABrock University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decades of research on the medicinal plant Catharanthus roseus have led to the complete elucidation of the 29-step pathway for the biosynthesis of the anticancer drug vinblastine from geraniol and tryptophan precursors. Several approaches have been used to identify the enzymes involved in this iconic and remarkably complex pathway. This chapter describes the use of the classic ethyl methanesulfonate (EMS) mutagenesis to create a selfed M2 mutant population, which can be rapidly screened to select mutants with altered monoterpenoid indole alkaloid (MIA) biosynthesis with a simple, high-throughput thin-layer chromatography (TLC)-based screening strategy. This TLC-based MIA screening has led to the discovery and characterization of three enzymes responsible for vinblastine biosynthesis.

Indexed as

CatharanthusSecologanin Tryptamine AlkaloidsChromatography, Thin LayerEthyl MethanesulfonateGene Expression Regulation, PlantPlant ProteinsVinblastineEthyl MethanesulfonatePlant ProteinsSecologanin Tryptamine AlkaloidsVinblastineCatharanthus roseusEMS mutagenesisMonoterpenoid indole alkaloid (MIA) biosynthesisThin-layer chromatography (TLC)

Identifiers

PMID35732945
OpenAlexW4285310138

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.